Name: rs2032678
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs2032678

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrY:13396820-13396830 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: delTTCTC
Variation Type: Indel Insertion and Deletion
Frequency: delTTCTC=0.02101 (634/30183, GnomAD)
delTTCTC=0.1646 (203/1233, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: UTY : Intron Variant
Publications: 4 citations
Genomic View: See rs on genome

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
gnomAD - Genomes	Global	Study-wide	30183	(CTTCT)₂C=0.97899	delTTCTC=0.02101
gnomAD - Genomes	European	Sub	16340	(CTTCT)₂C=0.99994	delTTCTC=0.00006
gnomAD - Genomes	African	Sub	8584	(CTTCT)₂C=0.9978	delTTCTC=0.0022
gnomAD - Genomes	American	Sub	3331	(CTTCT)₂C=0.9985	delTTCTC=0.0015
gnomAD - Genomes	Ashkenazi Jewish	Sub	750	(CTTCT)₂C=1.000	delTTCTC=0.000
gnomAD - Genomes	East Asian	Sub	714	(CTTCT)₂C=0.164	delTTCTC=0.836
gnomAD - Genomes	Other	Sub	464	(CTTCT)₂C=0.974	delTTCTC=0.026
1000Genomes	Global	Study-wide	1233	(CTTCT)₂C=0.8354	delTTCTC=0.1646
1000Genomes	African	Sub	319	(CTTCT)₂C=1.000	delTTCTC=0.000
1000Genomes	South Asian	Sub	260	(CTTCT)₂C=0.985	delTTCTC=0.015
1000Genomes	East Asian	Sub	244	(CTTCT)₂C=0.184	delTTCTC=0.816
1000Genomes	Europe	Sub	240	(CTTCT)₂C=1.000	delTTCTC=0.000
1000Genomes	American	Sub	170	(CTTCT)₂C=1.000	delTTCTC=0.000

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr Y	NC_000024.10:g.13396821TTCTC[1]
GRCh37.p13 chr Y	NC_000024.9:g.15508701TTCTC[1]

Gene: UTY, ubiquitously transcribed tetratricopeptide repeat containing, Y-linked (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
UTY transcript variant 4	NM_001258249.2:c.610+94_6… NM_001258249.2:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 5	NM_001258250.1:c.610+94_6… NM_001258250.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 6	NM_001258251.1:c.610+94_6… NM_001258251.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 7	NM_001258252.1:c.610+94_6… NM_001258252.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 8	NM_001258253.1:c.610+94_6… NM_001258253.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 9	NM_001258254.1:c.610+94_6… NM_001258254.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 10	NM_001258255.1:c.610+94_6… NM_001258255.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 11	NM_001258256.1:c.610+94_6… NM_001258256.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 12	NM_001258257.1:c.610+94_6… NM_001258257.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 13	NM_001258258.1:c.610+94_6… NM_001258258.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 14	NM_001258259.1:c.610+94_6… NM_001258259.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 15	NM_001258260.1:c.610+94_6… NM_001258260.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 16	NM_001258261.1:c.610+94_6… NM_001258261.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 17	NM_001258262.1:c.610+94_6… NM_001258262.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 18	NM_001258263.1:c.610+94_6… NM_001258263.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 19	NM_001258264.1:c.610+94_6… NM_001258264.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 20	NM_001258265.1:c.396+1416… NM_001258265.1:c.396+14169_396+14173del	N/A	Intron Variant
UTY transcript variant 21	NM_001258266.1:c.610+94_6… NM_001258266.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 22	NM_001258267.1:c.610+94_6… NM_001258267.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 23	NM_001258268.1:c.610+94_6… NM_001258268.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 24	NM_001258269.1:c.610+94_6… NM_001258269.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 25	NM_001258270.1:c.610+94_6… NM_001258270.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 78	NM_001400170.1:c.610+94_6… NM_001400170.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 79	NM_001400171.1:c.610+94_6… NM_001400171.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 80	NM_001400173.1:c.610+94_6… NM_001400173.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 81	NM_001400175.1:c.610+94_6… NM_001400175.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 82	NM_001400177.1:c.610+94_6… NM_001400177.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 83	NM_001400178.1:c.610+94_6… NM_001400178.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 84	NM_001400181.1:c.610+94_6… NM_001400181.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 85	NM_001400183.1:c.610+94_6… NM_001400183.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 86	NM_001400185.1:c.610+94_6… NM_001400185.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 87	NM_001400187.1:c.610+94_6… NM_001400187.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 88	NM_001400189.1:c.610+94_6… NM_001400189.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 89	NM_001400192.1:c.610+94_6… NM_001400192.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 90	NM_001400195.1:c.610+94_6… NM_001400195.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 91	NM_001400199.1:c.610+94_6… NM_001400199.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 3	NM_007125.4:c.610+94_610+… NM_007125.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 2	NM_182659.1:c.610+94_610+… NM_182659.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 1	NM_182660.1:c.610+94_610+… NM_182660.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant 26	NR_047596.1:n.	N/A	Intron Variant
UTY transcript variant 27	NR_047597.1:n.	N/A	Intron Variant
UTY transcript variant 28	NR_047598.1:n.	N/A	Intron Variant
UTY transcript variant 29	NR_047599.1:n.	N/A	Intron Variant
UTY transcript variant 30	NR_047600.1:n.	N/A	Intron Variant
UTY transcript variant 31	NR_047601.1:n.	N/A	Intron Variant
UTY transcript variant 32	NR_047602.1:n.	N/A	Intron Variant
UTY transcript variant 33	NR_047603.1:n.	N/A	Intron Variant
UTY transcript variant 34	NR_047604.1:n.	N/A	Intron Variant
UTY transcript variant 35	NR_047605.1:n.	N/A	Intron Variant
UTY transcript variant 36	NR_047606.1:n.	N/A	Intron Variant
UTY transcript variant 37	NR_047607.1:n.	N/A	Intron Variant
UTY transcript variant 38	NR_047608.1:n.	N/A	Intron Variant
UTY transcript variant 39	NR_047609.1:n.	N/A	Intron Variant
UTY transcript variant 40	NR_047610.1:n.	N/A	Intron Variant
UTY transcript variant 41	NR_047611.1:n.	N/A	Intron Variant
UTY transcript variant 42	NR_047612.1:n.	N/A	Intron Variant
UTY transcript variant 43	NR_047613.1:n.	N/A	Intron Variant
UTY transcript variant 44	NR_047614.1:n.	N/A	Intron Variant
UTY transcript variant 45	NR_047615.1:n.	N/A	Intron Variant
UTY transcript variant 46	NR_047616.1:n.	N/A	Intron Variant
UTY transcript variant 47	NR_047617.1:n.	N/A	Intron Variant
UTY transcript variant 48	NR_047618.1:n.	N/A	Intron Variant
UTY transcript variant 49	NR_047619.1:n.	N/A	Intron Variant
UTY transcript variant 50	NR_047620.1:n.	N/A	Intron Variant
UTY transcript variant 51	NR_047621.1:n.	N/A	Intron Variant
UTY transcript variant 52	NR_047622.1:n.	N/A	Intron Variant
UTY transcript variant 53	NR_047623.1:n.	N/A	Intron Variant
UTY transcript variant 54	NR_047624.1:n.	N/A	Intron Variant
UTY transcript variant 55	NR_047625.1:n.	N/A	Intron Variant
UTY transcript variant 56	NR_047626.1:n.	N/A	Intron Variant
UTY transcript variant 57	NR_047627.1:n.	N/A	Intron Variant
UTY transcript variant 58	NR_047628.1:n.	N/A	Intron Variant
UTY transcript variant 59	NR_047629.1:n.	N/A	Intron Variant
UTY transcript variant 60	NR_047630.1:n.	N/A	Intron Variant
UTY transcript variant 61	NR_047631.1:n.	N/A	Intron Variant
UTY transcript variant 62	NR_047632.1:n.	N/A	Intron Variant
UTY transcript variant 63	NR_047633.1:n.	N/A	Intron Variant
UTY transcript variant 64	NR_047634.1:n.	N/A	Intron Variant
UTY transcript variant 65	NR_047635.1:n.	N/A	Intron Variant
UTY transcript variant 66	NR_047636.1:n.	N/A	Intron Variant
UTY transcript variant 67	NR_047637.1:n.	N/A	Intron Variant
UTY transcript variant 68	NR_047638.1:n.	N/A	Intron Variant
UTY transcript variant 69	NR_047639.1:n.	N/A	Intron Variant
UTY transcript variant 70	NR_047640.1:n.	N/A	Intron Variant
UTY transcript variant 71	NR_047641.1:n.	N/A	Intron Variant
UTY transcript variant 72	NR_047642.1:n.	N/A	Intron Variant
UTY transcript variant 73	NR_047643.1:n.	N/A	Intron Variant
UTY transcript variant 74	NR_047644.1:n.	N/A	Intron Variant
UTY transcript variant 75	NR_047645.1:n.	N/A	Intron Variant
UTY transcript variant 76	NR_047646.1:n.	N/A	Intron Variant
UTY transcript variant 77	NR_047647.1:n.	N/A	Intron Variant
UTY transcript variant 92	NR_174404.1:n.	N/A	Intron Variant
UTY transcript variant 93	NR_174405.1:n.	N/A	Intron Variant
UTY transcript variant X1	XM_011531441.4:c.610+94_6… XM_011531441.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X2	XM_011531442.4:c.610+94_6… XM_011531442.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X3	XM_011531443.4:c.610+94_6… XM_011531443.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X5	XM_011531445.4:c.610+94_6… XM_011531445.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X6	XM_011531446.4:c.610+94_6… XM_011531446.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X7	XM_011531447.4:c.610+94_6… XM_011531447.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X8	XM_011531448.4:c.610+94_6… XM_011531448.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X9	XM_011531451.4:c.610+94_6… XM_011531451.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X10	XM_011531453.4:c.610+94_6… XM_011531453.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X11	XM_011531454.4:c.610+94_6… XM_011531454.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X12	XM_011531455.4:c.610+94_6… XM_011531455.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X21	XM_011531459.4:c.610+94_6… XM_011531459.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X26	XM_011531460.4:c.610+94_6… XM_011531460.4:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X24	XM_017030070.3:c.610+94_6… XM_017030070.3:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X29	XM_017030071.3:c.610+94_6… XM_017030071.3:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X30	XM_017030073.3:c.610+94_6… XM_017030073.3:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X4	XM_047442746.1:c.610+94_6… XM_047442746.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X13	XM_047442747.1:c.610+94_6… XM_047442747.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X14	XM_047442748.1:c.610+94_6… XM_047442748.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X15	XM_047442749.1:c.610+94_6… XM_047442749.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X16	XM_047442750.1:c.610+94_6… XM_047442750.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X17	XM_047442751.1:c.610+94_6… XM_047442751.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X18	XM_047442752.1:c.610+94_6… XM_047442752.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X19	XM_047442753.1:c.610+94_6… XM_047442753.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X20	XM_047442754.1:c.610+94_6… XM_047442754.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X22	XM_047442755.1:c.610+94_6… XM_047442755.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X27	XM_047442756.1:c.610+94_6… XM_047442756.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X28	XM_047442757.1:c.610+94_6… XM_047442757.1:c.610+94_610+98del	N/A	Intron Variant
UTY transcript variant X23	XR_007068451.1:n.	N/A	Intron Variant
UTY transcript variant X25	XR_007068452.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(CTTCT)₂C=	delTTCTC
GRCh38.p14 chr Y	NC_000024.10:g.13396820_13396830=	NC_000024.10:g.13396821TTCTC[1]
GRCh37.p13 chr Y	NC_000024.9:g.15508700_15508710=	NC_000024.9:g.15508701TTCTC[1]
UTY transcript variant 4	NM_001258249.1:c.610+98=	NM_001258249.1:c.610+94_610+98del
UTY transcript variant 4	NM_001258249.2:c.610+98=	NM_001258249.2:c.610+94_610+98del
UTY transcript variant 5	NM_001258250.1:c.610+98=	NM_001258250.1:c.610+94_610+98del
UTY transcript variant 6	NM_001258251.1:c.610+98=	NM_001258251.1:c.610+94_610+98del
UTY transcript variant 7	NM_001258252.1:c.610+98=	NM_001258252.1:c.610+94_610+98del
UTY transcript variant 8	NM_001258253.1:c.610+98=	NM_001258253.1:c.610+94_610+98del
UTY transcript variant 9	NM_001258254.1:c.610+98=	NM_001258254.1:c.610+94_610+98del
UTY transcript variant 10	NM_001258255.1:c.610+98=	NM_001258255.1:c.610+94_610+98del
UTY transcript variant 11	NM_001258256.1:c.610+98=	NM_001258256.1:c.610+94_610+98del
UTY transcript variant 12	NM_001258257.1:c.610+98=	NM_001258257.1:c.610+94_610+98del
UTY transcript variant 13	NM_001258258.1:c.610+98=	NM_001258258.1:c.610+94_610+98del
UTY transcript variant 14	NM_001258259.1:c.610+98=	NM_001258259.1:c.610+94_610+98del
UTY transcript variant 15	NM_001258260.1:c.610+98=	NM_001258260.1:c.610+94_610+98del
UTY transcript variant 16	NM_001258261.1:c.610+98=	NM_001258261.1:c.610+94_610+98del
UTY transcript variant 17	NM_001258262.1:c.610+98=	NM_001258262.1:c.610+94_610+98del
UTY transcript variant 18	NM_001258263.1:c.610+98=	NM_001258263.1:c.610+94_610+98del
UTY transcript variant 19	NM_001258264.1:c.610+98=	NM_001258264.1:c.610+94_610+98del
UTY transcript variant 20	NM_001258265.1:c.396+14173=	NM_001258265.1:c.396+14169_396+14173del
UTY transcript variant 21	NM_001258266.1:c.610+98=	NM_001258266.1:c.610+94_610+98del
UTY transcript variant 22	NM_001258267.1:c.610+98=	NM_001258267.1:c.610+94_610+98del
UTY transcript variant 23	NM_001258268.1:c.610+98=	NM_001258268.1:c.610+94_610+98del
UTY transcript variant 24	NM_001258269.1:c.610+98=	NM_001258269.1:c.610+94_610+98del
UTY transcript variant 25	NM_001258270.1:c.610+98=	NM_001258270.1:c.610+94_610+98del
UTY transcript variant 78	NM_001400170.1:c.610+98=	NM_001400170.1:c.610+94_610+98del
UTY transcript variant 79	NM_001400171.1:c.610+98=	NM_001400171.1:c.610+94_610+98del
UTY transcript variant 80	NM_001400173.1:c.610+98=	NM_001400173.1:c.610+94_610+98del
UTY transcript variant 81	NM_001400175.1:c.610+98=	NM_001400175.1:c.610+94_610+98del
UTY transcript variant 82	NM_001400177.1:c.610+98=	NM_001400177.1:c.610+94_610+98del
UTY transcript variant 83	NM_001400178.1:c.610+98=	NM_001400178.1:c.610+94_610+98del
UTY transcript variant 84	NM_001400181.1:c.610+98=	NM_001400181.1:c.610+94_610+98del
UTY transcript variant 85	NM_001400183.1:c.610+98=	NM_001400183.1:c.610+94_610+98del
UTY transcript variant 86	NM_001400185.1:c.610+98=	NM_001400185.1:c.610+94_610+98del
UTY transcript variant 87	NM_001400187.1:c.610+98=	NM_001400187.1:c.610+94_610+98del
UTY transcript variant 88	NM_001400189.1:c.610+98=	NM_001400189.1:c.610+94_610+98del
UTY transcript variant 89	NM_001400192.1:c.610+98=	NM_001400192.1:c.610+94_610+98del
UTY transcript variant 90	NM_001400195.1:c.610+98=	NM_001400195.1:c.610+94_610+98del
UTY transcript variant 91	NM_001400199.1:c.610+98=	NM_001400199.1:c.610+94_610+98del
UTY transcript variant 3	NM_007125.4:c.610+98=	NM_007125.4:c.610+94_610+98del
UTY transcript variant 2	NM_182659.1:c.610+98=	NM_182659.1:c.610+94_610+98del
UTY transcript variant 1	NM_182660.1:c.610+98=	NM_182660.1:c.610+94_610+98del
UTY transcript variant X1	XM_005262518.1:c.610+98=	XM_005262518.1:c.610+94_610+98del
UTY transcript variant X2	XM_005262519.1:c.9+98=	XM_005262519.1:c.9+94_9+98del
UTY transcript variant X3	XM_005262520.1:c.610+98=	XM_005262520.1:c.610+94_610+98del
UTY transcript variant X4	XM_005262521.1:c.610+98=	XM_005262521.1:c.610+94_610+98del
UTY transcript variant X5	XM_005262522.1:c.555+14173=	XM_005262522.1:c.555+14169_555+14173del
UTY transcript variant X6	XM_005262523.1:c.610+98=	XM_005262523.1:c.610+94_610+98del
UTY transcript variant X7	XM_005262524.1:c.9+98=	XM_005262524.1:c.9+94_9+98del
UTY transcript variant X8	XM_005262525.1:c.610+98=	XM_005262525.1:c.610+94_610+98del
UTY transcript variant X9	XM_005262526.1:c.610+98=	XM_005262526.1:c.610+94_610+98del
UTY transcript variant X10	XM_005262527.1:c.610+98=	XM_005262527.1:c.610+94_610+98del
UTY transcript variant X11	XM_005262528.1:c.-135+98=	XM_005262528.1:c.-135+94_-135+98del
UTY transcript variant X12	XM_005262529.1:c.610+98=	XM_005262529.1:c.610+94_610+98del
UTY transcript variant X13	XM_005262530.1:c.-135+98=	XM_005262530.1:c.-135+94_-135+98del
UTY transcript variant X14	XM_005262531.1:c.610+98=	XM_005262531.1:c.610+94_610+98del
UTY transcript variant X15	XM_005262532.1:c.610+98=	XM_005262532.1:c.610+94_610+98del
UTY transcript variant X16	XM_005262533.1:c.610+98=	XM_005262533.1:c.610+94_610+98del
UTY transcript variant X17	XM_005262534.1:c.610+98=	XM_005262534.1:c.610+94_610+98del
UTY transcript variant X18	XM_005262535.1:c.610+98=	XM_005262535.1:c.610+94_610+98del
UTY transcript variant X19	XM_005262536.1:c.555+14173=	XM_005262536.1:c.555+14169_555+14173del
UTY transcript variant X20	XM_005262537.1:c.610+98=	XM_005262537.1:c.610+94_610+98del
UTY transcript variant X21	XM_005262538.1:c.-130+98=	XM_005262538.1:c.-130+94_-130+98del
UTY transcript variant X22	XM_005262539.1:c.-95+98=	XM_005262539.1:c.-95+94_-95+98del
UTY transcript variant X23	XM_005262540.1:c.610+98=	XM_005262540.1:c.610+94_610+98del
UTY transcript variant X24	XM_005262541.1:c.-341+98=	XM_005262541.1:c.-341+94_-341+98del
UTY transcript variant X25	XM_005262542.1:c.-257+98=	XM_005262542.1:c.-257+94_-257+98del
UTY transcript variant X26	XM_005262543.1:c.610+98=	XM_005262543.1:c.610+94_610+98del
UTY transcript variant X27	XM_005262544.1:c.610+98=	XM_005262544.1:c.610+94_610+98del
UTY transcript variant X28	XM_005262545.1:c.610+98=	XM_005262545.1:c.610+94_610+98del
UTY transcript variant X29	XM_005262546.1:c.610+98=	XM_005262546.1:c.610+94_610+98del
UTY transcript variant X30	XM_005262547.1:c.-511+98=	XM_005262547.1:c.-511+94_-511+98del
UTY transcript variant X31	XM_005262548.1:c.610+98=	XM_005262548.1:c.610+94_610+98del
UTY transcript variant X32	XM_005262549.1:c.610+98=	XM_005262549.1:c.610+94_610+98del
UTY transcript variant X33	XM_005262550.1:c.610+98=	XM_005262550.1:c.610+94_610+98del
UTY transcript variant X34	XM_005262551.1:c.610+98=	XM_005262551.1:c.610+94_610+98del
UTY transcript variant X35	XM_005262552.1:c.555+14173=	XM_005262552.1:c.555+14169_555+14173del
UTY transcript variant X36	XM_005262553.1:c.610+98=	XM_005262553.1:c.610+94_610+98del
UTY transcript variant X37	XM_005262554.1:c.610+98=	XM_005262554.1:c.610+94_610+98del
UTY transcript variant X38	XM_005262555.1:c.-949+98=	XM_005262555.1:c.-949+94_-949+98del
UTY transcript variant X39	XM_005262556.1:c.217-60485=	XM_005262556.1:c.217-60489_217-60485del
UTY transcript variant X40	XM_005262557.1:c.610+98=	XM_005262557.1:c.610+94_610+98del
UTY transcript variant X41	XM_005262558.1:c.-1007+98=	XM_005262558.1:c.-1007+94_-1007+98del
UTY transcript variant X42	XM_005262559.1:c.-511+98=	XM_005262559.1:c.-511+94_-511+98del
UTY transcript variant X1	XM_011531441.4:c.610+98=	XM_011531441.4:c.610+94_610+98del
UTY transcript variant X2	XM_011531442.4:c.610+98=	XM_011531442.4:c.610+94_610+98del
UTY transcript variant X3	XM_011531443.4:c.610+98=	XM_011531443.4:c.610+94_610+98del
UTY transcript variant X5	XM_011531445.4:c.610+98=	XM_011531445.4:c.610+94_610+98del
UTY transcript variant X6	XM_011531446.4:c.610+98=	XM_011531446.4:c.610+94_610+98del
UTY transcript variant X7	XM_011531447.4:c.610+98=	XM_011531447.4:c.610+94_610+98del
UTY transcript variant X8	XM_011531448.4:c.610+98=	XM_011531448.4:c.610+94_610+98del
UTY transcript variant X9	XM_011531451.4:c.610+98=	XM_011531451.4:c.610+94_610+98del
UTY transcript variant X10	XM_011531453.4:c.610+98=	XM_011531453.4:c.610+94_610+98del
UTY transcript variant X11	XM_011531454.4:c.610+98=	XM_011531454.4:c.610+94_610+98del
UTY transcript variant X12	XM_011531455.4:c.610+98=	XM_011531455.4:c.610+94_610+98del
UTY transcript variant X21	XM_011531459.4:c.610+98=	XM_011531459.4:c.610+94_610+98del
UTY transcript variant X26	XM_011531460.4:c.610+98=	XM_011531460.4:c.610+94_610+98del
UTY transcript variant X24	XM_017030070.3:c.610+98=	XM_017030070.3:c.610+94_610+98del
UTY transcript variant X29	XM_017030071.3:c.610+98=	XM_017030071.3:c.610+94_610+98del
UTY transcript variant X30	XM_017030073.3:c.610+98=	XM_017030073.3:c.610+94_610+98del
UTY transcript variant X4	XM_047442746.1:c.610+98=	XM_047442746.1:c.610+94_610+98del
UTY transcript variant X13	XM_047442747.1:c.610+98=	XM_047442747.1:c.610+94_610+98del
UTY transcript variant X14	XM_047442748.1:c.610+98=	XM_047442748.1:c.610+94_610+98del
UTY transcript variant X15	XM_047442749.1:c.610+98=	XM_047442749.1:c.610+94_610+98del
UTY transcript variant X16	XM_047442750.1:c.610+98=	XM_047442750.1:c.610+94_610+98del
UTY transcript variant X17	XM_047442751.1:c.610+98=	XM_047442751.1:c.610+94_610+98del
UTY transcript variant X18	XM_047442752.1:c.610+98=	XM_047442752.1:c.610+94_610+98del
UTY transcript variant X19	XM_047442753.1:c.610+98=	XM_047442753.1:c.610+94_610+98del
UTY transcript variant X20	XM_047442754.1:c.610+98=	XM_047442754.1:c.610+94_610+98del
UTY transcript variant X22	XM_047442755.1:c.610+98=	XM_047442755.1:c.610+94_610+98del
UTY transcript variant X27	XM_047442756.1:c.610+98=	XM_047442756.1:c.610+94_610+98del
UTY transcript variant X28	XM_047442757.1:c.610+98=	XM_047442757.1:c.610+94_610+98del

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

13 SubSNP, 2 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	OEFNER	ss2941642	Apr 12, 2001 (94)
2	GMI	ss155886603	Dec 01, 2009 (131)
3	GMI	ss478865968	May 04, 2012 (137)
4	SSMP	ss664588586	Apr 01, 2015 (144)
5	1000GENOMES	ss1556752156	Apr 01, 2015 (144)
6	SYSTEMSBIOZJU	ss2629804711	Nov 08, 2017 (151)
7	KHV_HUMAN_GENOMES	ss3823535506	Jul 14, 2019 (153)
8	EVA	ss3986888953	Apr 27, 2021 (155)
9	GNOMAD	ss4126138630	Apr 27, 2021 (155)
10	HUGCELL_USP	ss5505742953	Oct 17, 2022 (156)
11	SANFORD_IMAGENETICS	ss5666137361	Oct 17, 2022 (156)
12	YY_MCH	ss5819515030	Oct 17, 2022 (156)
13	EVA	ss5857247085	Oct 17, 2022 (156)
14	1000Genomes	NC_000024.9 - 15508700	Oct 12, 2018 (152)
15	gnomAD - Genomes	NC_000024.10 - 13396820	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss478865968	NC_000024.8:14018093:CTTCT:	NC_000024.10:13396819:CTTCTCTTCTC:… NC_000024.10:13396819:CTTCTCTTCTC:CTTCTC	(self)
84705144, ss664588586, ss1556752156, ss2629804711, ss3986888953, ss5666137361	NC_000024.9:15508699:CTTCT:	NC_000024.10:13396819:CTTCTCTTCTC:… NC_000024.10:13396819:CTTCTCTTCTC:CTTCTC	(self)
594972505, ss3823535506, ss4126138630, ss5505742953, ss5819515030, ss5857247085	NC_000024.10:13396819:CTTCT:	NC_000024.10:13396819:CTTCTCTTCTC:… NC_000024.10:13396819:CTTCTCTTCTC:CTTCTC	(self)
ss2941642, ss155886603	NT_011875.12:1710127:TTCTC:	NC_000024.10:13396819:CTTCTCTTCTC:… NC_000024.10:13396819:CTTCTCTTCTC:CTTCTC	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

4 citations for rs2032678

PMID	Title	Author	Year	Journal
28445836	A forensic multiplex of nine novel pentameric-repeat STRs.	de la Puente M et al.	2017	Forensic science international. Genetics
31056738	Forensic features and genetic structure of 23 autosomal STRs in Artux Turkic-speaking population residing in southwestern Xinjiang Uyghur Autonomous Region.	Chen P et al.	2019	International journal of legal medicine
31437781	Pilot study for forensic evaluations of the Precision ID GlobalFiler™ NGS STR Panel v2 with the Ion S5™ system.	Tao R et al.	2019	Forensic science international. Genetics
31665944	Genetic admixture history and forensic characteristics of Turkic-speaking Kyrgyz population via 23 autosomal STRs.	Chen P et al.	2019	Annals of human biology

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs2032678