Name: rs2032667
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.

rs2032667

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrY:13324436 (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: G>A
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.02649 (1892/71418, ALFA)
A=0.00835 (250/29957, GnomAD)
A=0.0150 (24/1599, 1000G_30x) (+ 7 more)
A=0.0162 (20/1233, 1000G)
A=0.021 (19/895, chrY)
A=0.020 (16/816, Daghestan)
A=0.000 (0/160, HapMap)
A=0.04 (2/53, Qatari)
A=0.4 (4/10, Ancient Sardinia)
G=0.0 (0/6, SGDP_PRJ)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: UTY : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	71418	G=0.97351	A=0.02649
European	Sub	63268	G=0.97185	A=0.02815
African	Sub	1296	G=0.9923	A=0.0077
African Others	Sub	58	G=1.00	A=0.00
African American	Sub	1238	G=0.9919	A=0.0081
Asian	Sub	1756	G=0.9966	A=0.0034
East Asian	Sub	1394	G=0.9957	A=0.0043
Other Asian	Sub	362	G=1.000	A=0.000
Latin American 1	Sub	294	G=0.973	A=0.027
Latin American 2	Sub	1446	G=0.9938	A=0.0062
South Asian	Sub	132	G=0.955	A=0.045
Other	Sub	3226	G=0.9777	A=0.0223

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
Allele Frequency Aggregator	Total	Global	71418	G=0.97351	A=0.02649
Allele Frequency Aggregator	European	Sub	63268	G=0.97185	A=0.02815
Allele Frequency Aggregator	Other	Sub	3226	G=0.9777	A=0.0223
Allele Frequency Aggregator	Asian	Sub	1756	G=0.9966	A=0.0034
Allele Frequency Aggregator	Latin American 2	Sub	1446	G=0.9938	A=0.0062
Allele Frequency Aggregator	African	Sub	1296	G=0.9923	A=0.0077
Allele Frequency Aggregator	Latin American 1	Sub	294	G=0.973	A=0.027
Allele Frequency Aggregator	South Asian	Sub	132	G=0.955	A=0.045
gnomAD - Genomes	Global	Study-wide	29957	G=0.99165	A=0.00835
gnomAD - Genomes	European	Sub	16196	G=0.98994	A=0.01006
gnomAD - Genomes	African	Sub	8524	G=0.9971	A=0.0029
gnomAD - Genomes	American	Sub	3259	G=0.9899	A=0.0101
gnomAD - Genomes	East Asian	Sub	785	G=1.000	A=0.000
gnomAD - Genomes	Ashkenazi Jewish	Sub	744	G=0.966	A=0.034
gnomAD - Genomes	Other	Sub	449	G=0.991	A=0.009
1000Genomes_30x	Global	Study-wide	1599	G=0.9850	A=0.0150
1000Genomes_30x	African	Sub	458	G=1.000	A=0.000
1000Genomes_30x	South Asian	Sub	319	G=0.956	A=0.044
1000Genomes_30x	Europe	Sub	305	G=0.967	A=0.033
1000Genomes_30x	East Asian	Sub	292	G=1.000	A=0.000
1000Genomes_30x	American	Sub	225	G=1.000	A=0.000
1000Genomes	Global	Study-wide	1233	G=0.9838	A=0.0162
1000Genomes	African	Sub	319	G=1.000	A=0.000
1000Genomes	South Asian	Sub	260	G=0.954	A=0.046
1000Genomes	East Asian	Sub	244	G=1.000	A=0.000
1000Genomes	Europe	Sub	240	G=0.967	A=0.033
1000Genomes	American	Sub	170	G=1.000	A=0.000
chrY_custom_capture	Global	Study-wide	895	G=0.979	A=0.021
chrY_custom_capture	AFP	Sub	0	G=0	A=0
chrY_custom_capture	AHG	Sub	0	G=0	A=0
chrY_custom_capture	ASC	Sub	0	G=0	A=0
chrY_custom_capture	ASE	Sub	0	G=0	A=0
chrY_custom_capture	AUS	Sub	0	G=0	A=0
chrY_custom_capture	BRI	Sub	0	G=0	A=0
chrY_custom_capture	ENV	Sub	0	G=0	A=0
chrY_custom_capture	ESC	Sub	0	G=0	A=0
chrY_custom_capture	ESE	Sub	0	G=0	A=0
chrY_custom_capture	ESW	Sub	0	G=0	A=0
chrY_custom_capture	MEX	Sub	0	G=0	A=0
chrY_custom_capture	MNE	Sub	0	G=0	A=0
chrY_custom_capture	SCA	Sub	0	G=0	A=0
Genome-wide autozygosity in Daghestan	Global	Study-wide	816	G=0.980	A=0.020
Genome-wide autozygosity in Daghestan	Daghestan	Sub	308	G=1.000	A=0.000
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	G=0.972	A=0.028
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	G=0.984	A=0.016
Genome-wide autozygosity in Daghestan	Europe	Sub	108	G=0.963	A=0.037
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	G=0.94	A=0.06
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	G=1.00	A=0.00
HapMap	Global	Study-wide	160	G=1.000	A=0.000
HapMap	African	Sub	60	G=1.00	A=0.00
HapMap	American	Sub	60	G=1.00	A=0.00
HapMap	Asian	Sub	40	G=1.00	A=0.00
Qatari	Global	Study-wide	53	G=0.96	A=0.04
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	10	G=0.6	A=0.4
SGDP_PRJ	Global	Study-wide	6	G=0.0	A=1.0

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.13324436G>A
GRCh37.p13 chr Y	NC_000024.9:g.15436316G>A

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.3070+165… NM_001258249.2:c.3070+165C>T	N/A	Intron Variant
UTY transcript variant 5	NM_001258250.1:c.2359+165… NM_001258250.1:c.2359+165C>T	N/A	Intron Variant
UTY transcript variant 6	NM_001258251.1:c.2827+165… NM_001258251.1:c.2827+165C>T	N/A	Intron Variant
UTY transcript variant 7	NM_001258252.1:c.2914+165… NM_001258252.1:c.2914+165C>T	N/A	Intron Variant
UTY transcript variant 8	NM_001258253.1:c.2827+165… NM_001258253.1:c.2827+165C>T	N/A	Intron Variant
UTY transcript variant 9	NM_001258254.1:c.2542+165… NM_001258254.1:c.2542+165C>T	N/A	Intron Variant
UTY transcript variant 10	NM_001258255.1:c.2542+165… NM_001258255.1:c.2542+165C>T	N/A	Intron Variant
UTY transcript variant 11	NM_001258256.1:c.2914+165… NM_001258256.1:c.2914+165C>T	N/A	Intron Variant
UTY transcript variant 12	NM_001258257.1:c.2407+165… NM_001258257.1:c.2407+165C>T	N/A	Intron Variant
UTY transcript variant 13	NM_001258258.1:c.2935+165… NM_001258258.1:c.2935+165C>T	N/A	Intron Variant
UTY transcript variant 14	NM_001258259.1:c.2731+165… NM_001258259.1:c.2731+165C>T	N/A	Intron Variant
UTY transcript variant 15	NM_001258260.1:c.2869+165… NM_001258260.1:c.2869+165C>T	N/A	Intron Variant
UTY transcript variant 16	NM_001258261.1:c.2905+165… NM_001258261.1:c.2905+165C>T	N/A	Intron Variant
UTY transcript variant 17	NM_001258262.1:c.2698+165… NM_001258262.1:c.2698+165C>T	N/A	Intron Variant
UTY transcript variant 18	NM_001258263.1:c.2779+165… NM_001258263.1:c.2779+165C>T	N/A	Intron Variant
UTY transcript variant 19	NM_001258264.1:c.2866+165… NM_001258264.1:c.2866+165C>T	N/A	Intron Variant
UTY transcript variant 20	NM_001258265.1:c.2530+165… NM_001258265.1:c.2530+165C>T	N/A	Intron Variant
UTY transcript variant 21	NM_001258266.1:c.2914+165… NM_001258266.1:c.2914+165C>T	N/A	Intron Variant
UTY transcript variant 22	NM_001258267.1:c.2779+165… NM_001258267.1:c.2779+165C>T	N/A	Intron Variant
UTY transcript variant 23	NM_001258268.1:c.2542+165… NM_001258268.1:c.2542+165C>T	N/A	Intron Variant
UTY transcript variant 24	NM_001258269.1:c.2632+165… NM_001258269.1:c.2632+165C>T	N/A	Intron Variant
UTY transcript variant 25	NM_001258270.1:c.2407+165… NM_001258270.1:c.2407+165C>T	N/A	Intron Variant
UTY transcript variant 78	NM_001400170.1:c.2914+165… NM_001400170.1:c.2914+165C>T	N/A	Intron Variant
UTY transcript variant 79	NM_001400171.1:c.2869+165… NM_001400171.1:c.2869+165C>T	N/A	Intron Variant
UTY transcript variant 80	NM_001400173.1:c.2779+165… NM_001400173.1:c.2779+165C>T	N/A	Intron Variant
UTY transcript variant 81	NM_001400175.1:c.3004+165… NM_001400175.1:c.3004+165C>T	N/A	Intron Variant
UTY transcript variant 82	NM_001400177.1:c.3004+165… NM_001400177.1:c.3004+165C>T	N/A	Intron Variant
UTY transcript variant 83	NM_001400178.1:c.2914+165… NM_001400178.1:c.2914+165C>T	N/A	Intron Variant
UTY transcript variant 84	NM_001400181.1:c.2779+165… NM_001400181.1:c.2779+165C>T	N/A	Intron Variant
UTY transcript variant 85	NM_001400183.1:c.3070+165… NM_001400183.1:c.3070+165C>T	N/A	Intron Variant
UTY transcript variant 86	NM_001400185.1:c.3004+165… NM_001400185.1:c.3004+165C>T	N/A	Intron Variant
UTY transcript variant 87	NM_001400187.1:c.2962+165… NM_001400187.1:c.2962+165C>T	N/A	Intron Variant
UTY transcript variant 88	NM_001400189.1:c.2917+165… NM_001400189.1:c.2917+165C>T	N/A	Intron Variant
UTY transcript variant 89	NM_001400192.1:c.2914+165… NM_001400192.1:c.2914+165C>T	N/A	Intron Variant
UTY transcript variant 90	NM_001400195.1:c.2869+165… NM_001400195.1:c.2869+165C>T	N/A	Intron Variant
UTY transcript variant 91	NM_001400199.1:c.2827+165… NM_001400199.1:c.2827+165C>T	N/A	Intron Variant
UTY transcript variant 3	NM_007125.4:c.2779+165C>T	N/A	Intron Variant
UTY transcript variant 2	NM_182659.1:c.2779+165C>T	N/A	Intron Variant
UTY transcript variant 1	NM_182660.1:c.2779+165C>T	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.3118+165… XM_011531441.4:c.3118+165C>T	N/A	Intron Variant
UTY transcript variant X2	XM_011531442.4:c.3070+165… XM_011531442.4:c.3070+165C>T	N/A	Intron Variant
UTY transcript variant X3	XM_011531443.4:c.3052+165… XM_011531443.4:c.3052+165C>T	N/A	Intron Variant
UTY transcript variant X5	XM_011531445.4:c.2983+165… XM_011531445.4:c.2983+165C>T	N/A	Intron Variant
UTY transcript variant X6	XM_011531446.4:c.2962+165… XM_011531446.4:c.2962+165C>T	N/A	Intron Variant
UTY transcript variant X7	XM_011531447.4:c.2935+165… XM_011531447.4:c.2935+165C>T	N/A	Intron Variant
UTY transcript variant X8	XM_011531448.4:c.2917+165… XM_011531448.4:c.2917+165C>T	N/A	Intron Variant
UTY transcript variant X9	XM_011531451.4:c.2827+165… XM_011531451.4:c.2827+165C>T	N/A	Intron Variant
UTY transcript variant X10	XM_011531453.4:c.3118+165… XM_011531453.4:c.3118+165C>T	N/A	Intron Variant
UTY transcript variant X11	XM_011531454.4:c.3118+165… XM_011531454.4:c.3118+165C>T	N/A	Intron Variant
UTY transcript variant X12	XM_011531455.4:c.3118+165… XM_011531455.4:c.3118+165C>T	N/A	Intron Variant
UTY transcript variant X21	XM_011531459.4:c.3118+165… XM_011531459.4:c.3118+165C>T	N/A	Intron Variant
UTY transcript variant X26	XM_011531460.4:c.3118+165… XM_011531460.4:c.3118+165C>T	N/A	Intron Variant
UTY transcript variant X24	XM_017030070.3:c.3118+165… XM_017030070.3:c.3118+165C>T	N/A	Intron Variant
UTY transcript variant X29	XM_017030071.3:c.3118+165… XM_017030071.3:c.3118+165C>T	N/A	Intron Variant
UTY transcript variant X30	XM_017030073.3:c.2827+165… XM_017030073.3:c.2827+165C>T	N/A	Intron Variant
UTY transcript variant X4	XM_047442746.1:c.3004+165… XM_047442746.1:c.3004+165C>T	N/A	Intron Variant
UTY transcript variant X13	XM_047442747.1:c.3070+165… XM_047442747.1:c.3070+165C>T	N/A	Intron Variant
UTY transcript variant X14	XM_047442748.1:c.3070+165… XM_047442748.1:c.3070+165C>T	N/A	Intron Variant
UTY transcript variant X15	XM_047442749.1:c.3004+165… XM_047442749.1:c.3004+165C>T	N/A	Intron Variant
UTY transcript variant X16	XM_047442750.1:c.2983+165… XM_047442750.1:c.2983+165C>T	N/A	Intron Variant
UTY transcript variant X17	XM_047442751.1:c.2962+165… XM_047442751.1:c.2962+165C>T	N/A	Intron Variant
UTY transcript variant X18	XM_047442752.1:c.2935+165… XM_047442752.1:c.2935+165C>T	N/A	Intron Variant
UTY transcript variant X19	XM_047442753.1:c.2914+165… XM_047442753.1:c.2914+165C>T	N/A	Intron Variant
UTY transcript variant X20	XM_047442754.1:c.2914+165… XM_047442754.1:c.2914+165C>T	N/A	Intron Variant
UTY transcript variant X22	XM_047442755.1:c.3070+165… XM_047442755.1:c.3070+165C>T	N/A	Intron Variant
UTY transcript variant X27	XM_047442756.1:c.2914+165… XM_047442756.1:c.2914+165C>T	N/A	Intron Variant
UTY transcript variant X28	XM_047442757.1:c.3052+165… XM_047442757.1:c.3052+165C>T	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	G=	A
GRCh38.p14 chr Y	NC_000024.10:g.13324436=	NC_000024.10:g.13324436G>A
GRCh37.p13 chr Y	NC_000024.9:g.15436316=	NC_000024.9:g.15436316G>A
UTY transcript variant 4	NM_001258249.1:c.3070+165=	NM_001258249.1:c.3070+165C>T
UTY transcript variant 4	NM_001258249.2:c.3070+165=	NM_001258249.2:c.3070+165C>T
UTY transcript variant 5	NM_001258250.1:c.2359+165=	NM_001258250.1:c.2359+165C>T
UTY transcript variant 6	NM_001258251.1:c.2827+165=	NM_001258251.1:c.2827+165C>T
UTY transcript variant 7	NM_001258252.1:c.2914+165=	NM_001258252.1:c.2914+165C>T
UTY transcript variant 8	NM_001258253.1:c.2827+165=	NM_001258253.1:c.2827+165C>T
UTY transcript variant 9	NM_001258254.1:c.2542+165=	NM_001258254.1:c.2542+165C>T
UTY transcript variant 10	NM_001258255.1:c.2542+165=	NM_001258255.1:c.2542+165C>T
UTY transcript variant 11	NM_001258256.1:c.2914+165=	NM_001258256.1:c.2914+165C>T
UTY transcript variant 12	NM_001258257.1:c.2407+165=	NM_001258257.1:c.2407+165C>T
UTY transcript variant 13	NM_001258258.1:c.2935+165=	NM_001258258.1:c.2935+165C>T
UTY transcript variant 14	NM_001258259.1:c.2731+165=	NM_001258259.1:c.2731+165C>T
UTY transcript variant 15	NM_001258260.1:c.2869+165=	NM_001258260.1:c.2869+165C>T
UTY transcript variant 16	NM_001258261.1:c.2905+165=	NM_001258261.1:c.2905+165C>T
UTY transcript variant 17	NM_001258262.1:c.2698+165=	NM_001258262.1:c.2698+165C>T
UTY transcript variant 18	NM_001258263.1:c.2779+165=	NM_001258263.1:c.2779+165C>T
UTY transcript variant 19	NM_001258264.1:c.2866+165=	NM_001258264.1:c.2866+165C>T
UTY transcript variant 20	NM_001258265.1:c.2530+165=	NM_001258265.1:c.2530+165C>T
UTY transcript variant 21	NM_001258266.1:c.2914+165=	NM_001258266.1:c.2914+165C>T
UTY transcript variant 22	NM_001258267.1:c.2779+165=	NM_001258267.1:c.2779+165C>T
UTY transcript variant 23	NM_001258268.1:c.2542+165=	NM_001258268.1:c.2542+165C>T
UTY transcript variant 24	NM_001258269.1:c.2632+165=	NM_001258269.1:c.2632+165C>T
UTY transcript variant 25	NM_001258270.1:c.2407+165=	NM_001258270.1:c.2407+165C>T
UTY transcript variant 78	NM_001400170.1:c.2914+165=	NM_001400170.1:c.2914+165C>T
UTY transcript variant 79	NM_001400171.1:c.2869+165=	NM_001400171.1:c.2869+165C>T
UTY transcript variant 80	NM_001400173.1:c.2779+165=	NM_001400173.1:c.2779+165C>T
UTY transcript variant 81	NM_001400175.1:c.3004+165=	NM_001400175.1:c.3004+165C>T
UTY transcript variant 82	NM_001400177.1:c.3004+165=	NM_001400177.1:c.3004+165C>T
UTY transcript variant 83	NM_001400178.1:c.2914+165=	NM_001400178.1:c.2914+165C>T
UTY transcript variant 84	NM_001400181.1:c.2779+165=	NM_001400181.1:c.2779+165C>T
UTY transcript variant 85	NM_001400183.1:c.3070+165=	NM_001400183.1:c.3070+165C>T
UTY transcript variant 86	NM_001400185.1:c.3004+165=	NM_001400185.1:c.3004+165C>T
UTY transcript variant 87	NM_001400187.1:c.2962+165=	NM_001400187.1:c.2962+165C>T
UTY transcript variant 88	NM_001400189.1:c.2917+165=	NM_001400189.1:c.2917+165C>T
UTY transcript variant 89	NM_001400192.1:c.2914+165=	NM_001400192.1:c.2914+165C>T
UTY transcript variant 90	NM_001400195.1:c.2869+165=	NM_001400195.1:c.2869+165C>T
UTY transcript variant 91	NM_001400199.1:c.2827+165=	NM_001400199.1:c.2827+165C>T
UTY transcript variant 3	NM_007125.4:c.2779+165=	NM_007125.4:c.2779+165C>T
UTY transcript variant 2	NM_182659.1:c.2779+165=	NM_182659.1:c.2779+165C>T
UTY transcript variant 1	NM_182660.1:c.2779+165=	NM_182660.1:c.2779+165C>T
UTY transcript variant X1	XM_005262518.1:c.2914+165=	XM_005262518.1:c.2914+165C>T
UTY transcript variant X2	XM_005262519.1:c.2278+165=	XM_005262519.1:c.2278+165C>T
UTY transcript variant X3	XM_005262520.1:c.3070+165=	XM_005262520.1:c.3070+165C>T
UTY transcript variant X4	XM_005262521.1:c.3004+165=	XM_005262521.1:c.3004+165C>T
UTY transcript variant X5	XM_005262522.1:c.2980+165=	XM_005262522.1:c.2980+165C>T
UTY transcript variant X6	XM_005262523.1:c.2962+165=	XM_005262523.1:c.2962+165C>T
UTY transcript variant X7	XM_005262524.1:c.2143+165=	XM_005262524.1:c.2143+165C>T
UTY transcript variant X8	XM_005262525.1:c.2917+165=	XM_005262525.1:c.2917+165C>T
UTY transcript variant X9	XM_005262526.1:c.2914+165=	XM_005262526.1:c.2914+165C>T
UTY transcript variant X10	XM_005262527.1:c.2869+165=	XM_005262527.1:c.2869+165C>T
UTY transcript variant X11	XM_005262528.1:c.2035+165=	XM_005262528.1:c.2035+165C>T
UTY transcript variant X12	XM_005262529.1:c.2827+165=	XM_005262529.1:c.2827+165C>T
UTY transcript variant X13	XM_005262530.1:c.2035+165=	XM_005262530.1:c.2035+165C>T
UTY transcript variant X14	XM_005262531.1:c.2779+165=	XM_005262531.1:c.2779+165C>T
UTY transcript variant X15	XM_005262532.1:c.2983+165=	XM_005262532.1:c.2983+165C>T
UTY transcript variant X16	XM_005262533.1:c.2731+165=	XM_005262533.1:c.2731+165C>T
UTY transcript variant X17	XM_005262534.1:c.2728+165=	XM_005262534.1:c.2728+165C>T
UTY transcript variant X18	XM_005262535.1:c.2698+165=	XM_005262535.1:c.2698+165C>T
UTY transcript variant X19	XM_005262536.1:c.2689+165=	XM_005262536.1:c.2689+165C>T
UTY transcript variant X20	XM_005262537.1:c.2680+165=	XM_005262537.1:c.2680+165C>T
UTY transcript variant X21	XM_005262538.1:c.2035+165=	XM_005262538.1:c.2035+165C>T
UTY transcript variant X22	XM_005262539.1:c.2035+165=	XM_005262539.1:c.2035+165C>T
UTY transcript variant X23	XM_005262540.1:c.2827+165=	XM_005262540.1:c.2827+165C>T
UTY transcript variant X24	XM_005262541.1:c.1786+165=	XM_005262541.1:c.1786+165C>T
UTY transcript variant X25	XM_005262542.1:c.1786+165=	XM_005262542.1:c.1786+165C>T
UTY transcript variant X26	XM_005262543.1:c.2680+165=	XM_005262543.1:c.2680+165C>T
UTY transcript variant X27	XM_005262544.1:c.2779+165=	XM_005262544.1:c.2779+165C>T
UTY transcript variant X28	XM_005262545.1:c.2770+165=	XM_005262545.1:c.2770+165C>T
UTY transcript variant X29	XM_005262546.1:c.2731+165=	XM_005262546.1:c.2731+165C>T
UTY transcript variant X30	XM_005262547.1:c.1717+165=	XM_005262547.1:c.1717+165C>T
UTY transcript variant X31	XM_005262548.1:c.2680+165=	XM_005262548.1:c.2680+165C>T
UTY transcript variant X32	XM_005262549.1:c.2635+165=	XM_005262549.1:c.2635+165C>T
UTY transcript variant X33	XM_005262550.1:c.2407+165=	XM_005262550.1:c.2407+165C>T
UTY transcript variant X34	XM_005262551.1:c.2359+165=	XM_005262551.1:c.2359+165C>T
UTY transcript variant X35	XM_005262552.1:c.2317+165=	XM_005262552.1:c.2317+165C>T
UTY transcript variant X36	XM_005262553.1:c.2308+165=	XM_005262553.1:c.2308+165C>T
UTY transcript variant X37	XM_005262554.1:c.2455+165=	XM_005262554.1:c.2455+165C>T
UTY transcript variant X38	XM_005262555.1:c.1414+165=	XM_005262555.1:c.1414+165C>T
UTY transcript variant X39	XM_005262556.1:c.1225+165=	XM_005262556.1:c.1225+165C>T
UTY transcript variant X40	XM_005262557.1:c.1102+165=	XM_005262557.1:c.1102+165C>T
UTY transcript variant X41	XM_005262558.1:c.1087+165=	XM_005262558.1:c.1087+165C>T
UTY transcript variant X42	XM_005262559.1:c.1717+165=	XM_005262559.1:c.1717+165C>T
UTY transcript variant X1	XM_011531441.4:c.3118+165=	XM_011531441.4:c.3118+165C>T
UTY transcript variant X2	XM_011531442.4:c.3070+165=	XM_011531442.4:c.3070+165C>T
UTY transcript variant X3	XM_011531443.4:c.3052+165=	XM_011531443.4:c.3052+165C>T
UTY transcript variant X5	XM_011531445.4:c.2983+165=	XM_011531445.4:c.2983+165C>T
UTY transcript variant X6	XM_011531446.4:c.2962+165=	XM_011531446.4:c.2962+165C>T
UTY transcript variant X7	XM_011531447.4:c.2935+165=	XM_011531447.4:c.2935+165C>T
UTY transcript variant X8	XM_011531448.4:c.2917+165=	XM_011531448.4:c.2917+165C>T
UTY transcript variant X9	XM_011531451.4:c.2827+165=	XM_011531451.4:c.2827+165C>T
UTY transcript variant X10	XM_011531453.4:c.3118+165=	XM_011531453.4:c.3118+165C>T
UTY transcript variant X11	XM_011531454.4:c.3118+165=	XM_011531454.4:c.3118+165C>T
UTY transcript variant X12	XM_011531455.4:c.3118+165=	XM_011531455.4:c.3118+165C>T
UTY transcript variant X21	XM_011531459.4:c.3118+165=	XM_011531459.4:c.3118+165C>T
UTY transcript variant X26	XM_011531460.4:c.3118+165=	XM_011531460.4:c.3118+165C>T
UTY transcript variant X24	XM_017030070.3:c.3118+165=	XM_017030070.3:c.3118+165C>T
UTY transcript variant X29	XM_017030071.3:c.3118+165=	XM_017030071.3:c.3118+165C>T
UTY transcript variant X30	XM_017030073.3:c.2827+165=	XM_017030073.3:c.2827+165C>T
UTY transcript variant X4	XM_047442746.1:c.3004+165=	XM_047442746.1:c.3004+165C>T
UTY transcript variant X13	XM_047442747.1:c.3070+165=	XM_047442747.1:c.3070+165C>T
UTY transcript variant X14	XM_047442748.1:c.3070+165=	XM_047442748.1:c.3070+165C>T
UTY transcript variant X15	XM_047442749.1:c.3004+165=	XM_047442749.1:c.3004+165C>T
UTY transcript variant X16	XM_047442750.1:c.2983+165=	XM_047442750.1:c.2983+165C>T
UTY transcript variant X17	XM_047442751.1:c.2962+165=	XM_047442751.1:c.2962+165C>T
UTY transcript variant X18	XM_047442752.1:c.2935+165=	XM_047442752.1:c.2935+165C>T
UTY transcript variant X19	XM_047442753.1:c.2914+165=	XM_047442753.1:c.2914+165C>T
UTY transcript variant X20	XM_047442754.1:c.2914+165=	XM_047442754.1:c.2914+165C>T
UTY transcript variant X22	XM_047442755.1:c.3070+165=	XM_047442755.1:c.3070+165C>T
UTY transcript variant X27	XM_047442756.1:c.2914+165=	XM_047442756.1:c.2914+165C>T
UTY transcript variant X28	XM_047442757.1:c.3052+165=	XM_047442757.1:c.3052+165C>T

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#.

60 SubSNP, 10 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	OEFNER	ss2941631	Apr 12, 2001 (94)
2	PERLEGEN	ss69277842	May 18, 2007 (127)
3	ILLUMINA	ss74982340	Dec 07, 2007 (129)
4	ILLUMINA	ss160491257	Dec 01, 2009 (131)
5	ILLUMINA	ss173056850	Jul 04, 2010 (132)
6	ILLUMINA	ss480389289	May 04, 2012 (137)
7	ILLUMINA	ss480402163	May 04, 2012 (137)
8	ILLUMINA	ss481180231	Sep 08, 2015 (146)
9	ILLUMINA	ss484992271	May 04, 2012 (137)
10	ILLUMINA	ss537025936	Oct 12, 2018 (152)
11	SSMP	ss663096920	Apr 25, 2013 (138)
12	ILLUMINA	ss778477417	Sep 08, 2015 (146)
13	ILLUMINA	ss782942434	Sep 08, 2015 (146)
14	ILLUMINA	ss783904980	Sep 08, 2015 (146)
15	ILLUMINA	ss832198109	Sep 08, 2015 (146)
16	ILLUMINA	ss833933255	Sep 08, 2015 (146)
17	HAMMER_LAB	ss1397804339	Sep 08, 2015 (146)
18	JOBLING_UOL	ss1399956940	Apr 01, 2015 (144)
19	1000GENOMES	ss1556751800	Apr 01, 2015 (144)
20	ILLUMINA	ss1752814420	Sep 08, 2015 (146)
21	WEILL_CORNELL_DGM	ss1939860894	Feb 12, 2016 (147)
22	ILLUMINA	ss1945968896	Feb 12, 2016 (147)
23	ILLUMINA	ss1958176710	Feb 12, 2016 (147)
24	ILLUMINA	ss2094838509	Dec 20, 2016 (150)
25	ILLUMINA	ss2095229579	Dec 20, 2016 (150)
26	HUMAN_LONGEVITY	ss2321412055	Dec 20, 2016 (150)
27	ILLUMINA	ss2634994045	Nov 08, 2017 (151)
28	ILLUMINA	ss2711191581	Nov 08, 2017 (151)
29	SWEGEN	ss3020948563	Nov 08, 2017 (151)
30	ILLUMINA	ss3023053327	Nov 08, 2017 (151)
31	ILLUMINA	ss3626005443	Oct 12, 2018 (152)
32	ILLUMINA	ss3630504401	Oct 12, 2018 (152)
33	ILLUMINA	ss3632876940	Oct 12, 2018 (152)
34	ILLUMINA	ss3633570648	Oct 12, 2018 (152)
35	ILLUMINA	ss3634300984	Oct 12, 2018 (152)
36	ILLUMINA	ss3635264778	Oct 12, 2018 (152)
37	ILLUMINA	ss3635977810	Oct 12, 2018 (152)
38	ILLUMINA	ss3637014903	Oct 12, 2018 (152)
39	ILLUMINA	ss3637731537	Oct 12, 2018 (152)
40	ILLUMINA	ss3638886733	Oct 12, 2018 (152)
41	ILLUMINA	ss3640972266	Oct 12, 2018 (152)
42	ILLUMINA	ss3641265972	Oct 12, 2018 (152)
43	ILLUMINA	ss3643809501	Oct 12, 2018 (152)
44	ILLUMINA	ss3645021415	Oct 12, 2018 (152)
45	ILLUMINA	ss3653611836	Oct 12, 2018 (152)
46	ILLUMINA	ss3726713395	Jul 14, 2019 (153)
47	ILLUMINA	ss3744336254	Jul 14, 2019 (153)
48	ILLUMINA	ss3745564792	Jul 14, 2019 (153)
49	ILLUMINA	ss3773056400	Jul 14, 2019 (153)
50	SGDP_PRJ	ss3892707918	Apr 27, 2020 (154)
51	EVA	ss3984772121	Apr 27, 2021 (155)
52	EVA	ss3985989250	Apr 27, 2021 (155)
53	GNOMAD	ss4126137054	Apr 27, 2021 (155)
54	EVA	ss5237629921	Apr 27, 2021 (155)
55	ESTONIANBIOCENTRE	ss5237681535	Oct 17, 2022 (156)
56	EVA	ss5316103792	Oct 17, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5623821484	Oct 17, 2022 (156)
58	SANFORD_IMAGENETICS	ss5666137262	Oct 17, 2022 (156)
59	EVA	ss5848242441	Oct 17, 2022 (156)
60	EVA	ss5979925333	Oct 17, 2022 (156)
61	1000Genomes	NC_000024.9 - 15436316	Oct 12, 2018 (152)
62	1000Genomes_30x	NC_000024.10 - 13324436	Oct 17, 2022 (156)
63	chrY_custom_capture	NC_000024.9 - 15436316	Apr 27, 2020 (154)
64	Genome-wide autozygosity in Daghestan	NC_000024.8 - 13945710	Apr 27, 2020 (154)
65	gnomAD - Genomes	NC_000024.10 - 13324436	Apr 27, 2021 (155)
66	HapMap	NC_000024.10 - 13324436	Apr 27, 2020 (154)
67	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000024.9 - 15436316	Apr 27, 2021 (155)
68	Qatari	NC_000024.9 - 15436316	Apr 27, 2020 (154)
69	SGDP_PRJ	NC_000024.9 - 15436316	Apr 27, 2020 (154)
70	ALFA	NC_000024.10 - 13324436	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
555512, ss480389289, ss1397804339, ss3643809501	NC_000024.8:13945709:G:A	NC_000024.10:13324435:G:A	(self)
84704788, 4215, 1215177, 21902816, 44724898, ss480402163, ss481180231, ss484992271, ss537025936, ss663096920, ss778477417, ss782942434, ss783904980, ss832198109, ss833933255, ss1399956940, ss1556751800, ss1752814420, ss1939860894, ss1945968896, ss1958176710, ss2094838509, ss2095229579, ss2634994045, ss2711191581, ss3020948563, ss3023053327, ss3626005443, ss3630504401, ss3632876940, ss3633570648, ss3634300984, ss3635264778, ss3635977810, ss3637014903, ss3637731537, ss3638886733, ss3640972266, ss3641265972, ss3645021415, ss3653611836, ss3744336254, ss3745564792, ss3773056400, ss3892707918, ss3984772121, ss3985989250, ss5237629921, ss5237681535, ss5316103792, ss5666137262, ss5848242441, ss5979925333	NC_000024.9:15436315:G:A	NC_000024.10:13324435:G:A	(self)
111347419, 594970928, 4060649, 1183812644, ss2321412055, ss3726713395, ss4126137054, ss5623821484	NC_000024.10:13324435:G:A	NC_000024.10:13324435:G:A	(self)
ss2941631, ss69277842, ss74982340, ss160491257, ss173056850	NT_011875.12:1637737:G:A	NC_000024.10:13324435:G:A	(self)

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

No publications for rs2032667

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs2032667