Name: rs34263964
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.

rs34263964

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:125841188-125841200 (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: delGT / dupGT / dupGTGT / dup(GT)₅
Variation Type: Indel Insertion and Deletion
Frequency: dup(GT)₅=0.000008 (2/264690, TOPMED)
dupGT=0.46288 (13080/28258, 14KJPN)
dupGT=0.45931 (7698/16760, 8.3KJPN) (+ 8 more)
dupGT=0.14863 (1508/10146, ALFA)
dupGT=0.3355 (1680/5008, 1000G)
dupGT=0.3330 (1492/4480, Estonian)
dupGT=0.4683 (858/1832, Korea1K)
dupGT=0.350 (349/998, GoNL)
dupGT=0.380 (228/600, NorthernSweden)
dupGT=0.486 (103/212, Vietnamese)
dupGT=0.35 (14/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BCCIP : Intron Variant
DHX32 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	10146	TGTGTGTGTGTGT=0.85137	TGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGT=0.14863, TGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGT=0.00000	0.751823	0.049083	0.199093	32
European	Sub	7804	TGTGTGTGTGTGT=0.8080	TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.1920, TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.679395	0.063301	0.257304	32
African	Sub	1742	TGTGTGTGTGTGT=0.9971	TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0029, TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.994259	0.0	0.005741	0
African Others	Sub	72	TGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1670	TGTGTGTGTGTGT=0.9970	TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0030, TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.994012	0.0	0.005988	0
Asian	Sub	26	TGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	20	TGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TGTGTGTGTGTGT=1.0	TGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	64	TGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	246	TGTGTGTGTGTGT=1.000	TGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	28	TGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other	Sub	236	TGTGTGTGTGTGT=0.979	TGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.021, TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000	0.974576	0.016949	0.008475	32

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
TopMed	Global	Study-wide	264690	- No frequency provided	dup(GT)₅=0.000008
14KJPN	JAPANESE	Study-wide	28258	- No frequency provided	dupGT=0.46288
8.3KJPN	JAPANESE	Study-wide	16760	- No frequency provided	dupGT=0.45931
Allele Frequency Aggregator	Total	Global	10146	(TG)₆T=0.85137	delGT=0.00000, dupGT=0.14863, dupGTGT=0.00000, dup(GT)₅=0.00000
Allele Frequency Aggregator	European	Sub	7804	(TG)₆T=0.8080	delGT=0.0000, dupGT=0.1920, dupGTGT=0.0000, dup(GT)₅=0.0000
Allele Frequency Aggregator	African	Sub	1742	(TG)₆T=0.9971	delGT=0.0000, dupGT=0.0029, dupGTGT=0.0000, dup(GT)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	246	(TG)₆T=1.000	delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₅=0.000
Allele Frequency Aggregator	Other	Sub	236	(TG)₆T=0.979	delGT=0.000, dupGT=0.021, dupGTGT=0.000, dup(GT)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	64	(TG)₆T=1.00	delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	28	(TG)₆T=1.00	delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₅=0.00
Allele Frequency Aggregator	Asian	Sub	26	(TG)₆T=1.00	delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₅=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupGT=0.3355
1000Genomes	African	Sub	1322	- No frequency provided	dupGT=0.2118
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupGT=0.5238
1000Genomes	Europe	Sub	1006	- No frequency provided	dupGT=0.3529
1000Genomes	South Asian	Sub	978	- No frequency provided	dupGT=0.335
1000Genomes	American	Sub	694	- No frequency provided	dupGT=0.272
Genetic variation in the Estonian population	Estonian	Study-wide	4480	- No frequency provided	dupGT=0.3330
Korean Genome Project	KOREAN	Study-wide	1832	- No frequency provided	dupGT=0.4683
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	- No frequency provided	dupGT=0.350
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupGT=0.380
A Vietnamese Genetic Variation Database	Global	Study-wide	212	- No frequency provided	dupGT=0.486
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupGT=0.35

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 10	NC_000010.11:g.125841189GT[5]
GRCh38.p14 chr 10	NC_000010.11:g.125841189GT[7]
GRCh38.p14 chr 10	NC_000010.11:g.125841189GT[8]
GRCh38.p14 chr 10	NC_000010.11:g.125841189GT[11]
GRCh37.p13 chr 10	NC_000010.10:g.127529758GT[5]
GRCh37.p13 chr 10	NC_000010.10:g.127529758GT[7]
GRCh37.p13 chr 10	NC_000010.10:g.127529758GT[8]
GRCh37.p13 chr 10	NC_000010.10:g.127529758GT[11]
BCCIP RefSeqGene	NG_029095.1:g.22655GT[5]
BCCIP RefSeqGene	NG_029095.1:g.22655GT[7]
BCCIP RefSeqGene	NG_029095.1:g.22655GT[8]
BCCIP RefSeqGene	NG_029095.1:g.22655GT[11]

Gene: BCCIP, BRCA2 and CDKN1A interacting protein (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BCCIP transcript variant A	NM_016567.4:c.775-67TG[5]	N/A	Intron Variant
BCCIP transcript variant C	NM_078469.3:c.775-67TG[5]	N/A	Intron Variant
BCCIP transcript variant B	NM_078468.3:c.	N/A	Genic Downstream Transcript Variant

Gene: DHX32, DEAH-box helicase 32 (putative) (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DHX32 transcript	NM_018180.3:c.1544-203CA[… NM_018180.3:c.1544-203CA[5]	N/A	Intron Variant
DHX32 transcript variant X1	XM_047425467.1:c.1691-203… XM_047425467.1:c.1691-203CA[5]	N/A	Intron Variant
DHX32 transcript variant X2	XM_047425468.1:c.1691-203… XM_047425468.1:c.1691-203CA[5]	N/A	Intron Variant
DHX32 transcript variant X3	XM_047425469.1:c.1544-203… XM_047425469.1:c.1544-203CA[5]	N/A	Intron Variant
DHX32 transcript variant X4	XM_047425470.1:c.1544-203… XM_047425470.1:c.1544-203CA[5]	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	(TG)₆T=	delGT	dupGT	dupGTGT	dup(GT)₅
GRCh38.p14 chr 10	NC_000010.11:g.125841188_125841200=	NC_000010.11:g.125841189GT[5]	NC_000010.11:g.125841189GT[7]	NC_000010.11:g.125841189GT[8]	NC_000010.11:g.125841189GT[11]
GRCh37.p13 chr 10	NC_000010.10:g.127529757_127529769=	NC_000010.10:g.127529758GT[5]	NC_000010.10:g.127529758GT[7]	NC_000010.10:g.127529758GT[8]	NC_000010.10:g.127529758GT[11]
BCCIP RefSeqGene	NG_029095.1:g.22654_22666=	NG_029095.1:g.22655GT[5]	NG_029095.1:g.22655GT[7]	NG_029095.1:g.22655GT[8]	NG_029095.1:g.22655GT[11]
BCCIP transcript variant A	NM_016567.3:c.775-67=	NM_016567.3:c.775-67TG[5]	NM_016567.3:c.775-67TG[7]	NM_016567.3:c.775-67TG[8]	NM_016567.3:c.775-67TG[11]
BCCIP transcript variant A	NM_016567.4:c.775-67=	NM_016567.4:c.775-67TG[5]	NM_016567.4:c.775-67TG[7]	NM_016567.4:c.775-67TG[8]	NM_016567.4:c.775-67TG[11]
DHX32 transcript	NM_018180.2:c.1544-192=	NM_018180.2:c.1544-203CA[5]	NM_018180.2:c.1544-203CA[7]	NM_018180.2:c.1544-203CA[8]	NM_018180.2:c.1544-203CA[11]
DHX32 transcript	NM_018180.3:c.1544-192=	NM_018180.3:c.1544-203CA[5]	NM_018180.3:c.1544-203CA[7]	NM_018180.3:c.1544-203CA[8]	NM_018180.3:c.1544-203CA[11]
BCCIP transcript variant C	NM_078469.2:c.775-67=	NM_078469.2:c.775-67TG[5]	NM_078469.2:c.775-67TG[7]	NM_078469.2:c.775-67TG[8]	NM_078469.2:c.775-67TG[11]
BCCIP transcript variant C	NM_078469.3:c.775-67=	NM_078469.3:c.775-67TG[5]	NM_078469.3:c.775-67TG[7]	NM_078469.3:c.775-67TG[8]	NM_078469.3:c.775-67TG[11]
BCCIP transcript variant X1	XM_005269982.1:c.775-73=	XM_005269982.1:c.775-73TG[5]	XM_005269982.1:c.775-73TG[7]	XM_005269982.1:c.775-73TG[8]	XM_005269982.1:c.775-73TG[11]
BCCIP transcript variant X2	XM_005269983.1:c.685-67=	XM_005269983.1:c.685-67TG[5]	XM_005269983.1:c.685-67TG[7]	XM_005269983.1:c.685-67TG[8]	XM_005269983.1:c.685-67TG[11]
DHX32 transcript variant X1	XM_047425467.1:c.1691-192=	XM_047425467.1:c.1691-203CA[5]	XM_047425467.1:c.1691-203CA[7]	XM_047425467.1:c.1691-203CA[8]	XM_047425467.1:c.1691-203CA[11]
DHX32 transcript variant X2	XM_047425468.1:c.1691-192=	XM_047425468.1:c.1691-203CA[5]	XM_047425468.1:c.1691-203CA[7]	XM_047425468.1:c.1691-203CA[8]	XM_047425468.1:c.1691-203CA[11]
DHX32 transcript variant X3	XM_047425469.1:c.1544-192=	XM_047425469.1:c.1544-203CA[5]	XM_047425469.1:c.1544-203CA[7]	XM_047425469.1:c.1544-203CA[8]	XM_047425469.1:c.1544-203CA[11]
DHX32 transcript variant X4	XM_047425470.1:c.1544-192=	XM_047425470.1:c.1544-203CA[5]	XM_047425470.1:c.1544-203CA[7]	XM_047425470.1:c.1544-203CA[8]	XM_047425470.1:c.1544-203CA[11]

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#.

61 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39743674	Mar 13, 2006 (126)
2	HGSV	ss81527854	Dec 03, 2013 (138)
3	HUMANGENOME_JCVI	ss95556148	Dec 05, 2013 (138)
4	BL	ss256143656	May 09, 2011 (134)
5	GMI	ss289044019	May 04, 2012 (137)
6	GMI	ss289044020	May 04, 2012 (137)
7	1000GENOMES	ss327292445	May 09, 2011 (134)
8	1000GENOMES	ss327376104	May 09, 2011 (134)
9	1000GENOMES	ss327771106	May 09, 2011 (134)
10	LUNTER	ss552080738	Apr 25, 2013 (138)
11	LUNTER	ss552331394	Apr 25, 2013 (138)
12	LUNTER	ss553432057	Apr 25, 2013 (138)
13	TISHKOFF	ss561451020	Apr 25, 2013 (138)
14	SSMP	ss663961261	Apr 01, 2015 (144)
15	EVA-GONL	ss988038175	Aug 21, 2014 (142)
16	1000GENOMES	ss1370266633	Aug 21, 2014 (142)
17	DDI	ss1536673279	Apr 01, 2015 (144)
18	EVA_GENOME_DK	ss1574274853	Apr 01, 2015 (144)
19	EVA_UK10K_ALSPAC	ss1706943036	Jan 10, 2018 (151)
20	EVA_UK10K_TWINSUK	ss1706943114	Jan 10, 2018 (151)
21	EVA_UK10K_ALSPAC	ss1710493941	Apr 01, 2015 (144)
22	EVA_UK10K_TWINSUK	ss1710493947	Apr 01, 2015 (144)
23	GENOMED	ss1967251933	Jul 19, 2016 (147)
24	JJLAB	ss2031050243	Sep 14, 2016 (149)
25	SYSTEMSBIOZJU	ss2627685596	Nov 08, 2017 (151)
26	SWEGEN	ss3007325506	Nov 08, 2017 (151)
27	MCHAISSO	ss3063674114	Nov 08, 2017 (151)
28	MCHAISSO	ss3064496632	Nov 08, 2017 (151)
29	MCHAISSO	ss3065408427	Nov 08, 2017 (151)
30	BIOINF_KMB_FNS_UNIBA	ss3645169501	Oct 12, 2018 (152)
31	URBANLAB	ss3649491736	Oct 12, 2018 (152)
32	EGCUT_WGS	ss3674746451	Jul 13, 2019 (153)
33	EVA_DECODE	ss3690902546	Jul 13, 2019 (153)
34	ACPOP	ss3737775364	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3814099645	Jul 13, 2019 (153)
36	EVA	ss3832390216	Apr 26, 2020 (154)
37	EVA	ss3839736330	Apr 26, 2020 (154)
38	EVA	ss3845211671	Apr 26, 2020 (154)
39	KOGIC	ss3968896464	Apr 26, 2020 (154)
40	FSA-LAB	ss3983988903	Apr 26, 2021 (155)
41	FSA-LAB	ss3983988904	Apr 26, 2021 (155)
42	EVA	ss3986502933	Apr 26, 2021 (155)
43	GNOMAD	ss4227558763	Apr 26, 2021 (155)
44	GNOMAD	ss4227558764	Apr 26, 2021 (155)
45	GNOMAD	ss4227558765	Apr 26, 2021 (155)
46	TOPMED	ss4870257022	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5199967861	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5285854429	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5285854430	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5481239919	Oct 16, 2022 (156)
51	EVA	ss5510205271	Oct 16, 2022 (156)
52	EVA	ss5623951000	Oct 16, 2022 (156)
53	EVA	ss5624013916	Oct 16, 2022 (156)
54	SANFORD_IMAGENETICS	ss5650316917	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5746489695	Oct 16, 2022 (156)
56	EVA	ss5800163313	Oct 16, 2022 (156)
57	YY_MCH	ss5811982571	Oct 16, 2022 (156)
58	EVA	ss5825111085	Oct 16, 2022 (156)
59	EVA	ss5848310549	Oct 16, 2022 (156)
60	EVA	ss5849790845	Oct 16, 2022 (156)
61	EVA	ss5880980549	Oct 16, 2022 (156)
62	1000Genomes	NC_000010.10 - 127529757	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 28872019 (NC_000010.10:127529756::TG 1355/3854) Row 28872020 (NC_000010.10:127529756:TG: 2/3854)	-	Oct 12, 2018 (152)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 28872019 (NC_000010.10:127529756::TG 1355/3854) Row 28872020 (NC_000010.10:127529756:TG: 2/3854)	-	Oct 12, 2018 (152)
65	Genetic variation in the Estonian population	NC_000010.10 - 127529757	Oct 12, 2018 (152)
66	The Danish reference pan genome	NC_000010.10 - 127529757	Apr 26, 2020 (154)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 367111433 (NC_000010.11:125841187::TG 43786/139786) Row 367111434 (NC_000010.11:125841187::TGTG 3/139886) Row 367111435 (NC_000010.11:125841187::TGTGTGTGTG 3/139886)	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 367111433 (NC_000010.11:125841187::TG 43786/139786) Row 367111434 (NC_000010.11:125841187::TGTG 3/139886) Row 367111435 (NC_000010.11:125841187::TGTGTGTGTG 3/139886)	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 367111433 (NC_000010.11:125841187::TG 43786/139786) Row 367111434 (NC_000010.11:125841187::TGTG 3/139886) Row 367111435 (NC_000010.11:125841187::TGTGTGTGTG 3/139886)	-	Apr 26, 2021 (155)
70	Genome of the Netherlands Release 5	NC_000010.10 - 127529757	Apr 26, 2020 (154)
71	Korean Genome Project	NC_000010.11 - 125841188	Apr 26, 2020 (154)
72	Northern Sweden	NC_000010.10 - 127529757	Jul 13, 2019 (153)
73	8.3KJPN	NC_000010.10 - 127529757	Apr 26, 2021 (155)
74	14KJPN	NC_000010.11 - 125841188	Oct 16, 2022 (156)
75	TopMed	NC_000010.11 - 125841188	Apr 26, 2021 (155)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 28872019 (NC_000010.10:127529756::TG 1267/3708) Row 28872020 (NC_000010.10:127529756:TG: 6/3708)	-	Oct 12, 2018 (152)
77	UK 10K study - Twins Submission ignored due to conflicting rows: Row 28872019 (NC_000010.10:127529756::TG 1267/3708) Row 28872020 (NC_000010.10:127529756:TG: 6/3708)	-	Oct 12, 2018 (152)
78	A Vietnamese Genetic Variation Database	NC_000010.10 - 127529757	Jul 13, 2019 (153)
79	ALFA	NC_000010.11 - 125841188	Apr 26, 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).

Associated ID	History Updated (Build)
rs370868705	May 15, 2013 (138)
rs796129899	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1706943036, ss1706943114, ss5510205271	NC_000010.10:127529756:TG:	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGT	(self)
ss5285854430	NC_000010.11:125841187:TG:	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGT
6110159782	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGT	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGT	(self)
ss256143656, ss289044019, ss327292445, ss327376104, ss327771106, ss552080738, ss552331394, ss553432057	NC_000010.9:127519746::TG	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss289044020	NC_000010.9:127519759::GT	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
51966825, 20484699, 271280, 12866960, 11060229, 57937168, 6407231, ss663961261, ss988038175, ss1370266633, ss1536673279, ss1574274853, ss1967251933, ss2031050243, ss2627685596, ss3007325506, ss3674746451, ss3737775364, ss3832390216, ss3839736330, ss3983988903, ss3986502933, ss5199967861, ss5623951000, ss5624013916, ss5650316917, ss5800163313, ss5825111085	NC_000010.10:127529756::TG	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss1710493941, ss1710493947	NC_000010.10:127529758::TG	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss561451020, ss3983988904, ss5848310549	NC_000010.10:127529769::GT	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
25274465, 80326799, ss3063674114, ss3064496632, ss3065408427, ss3645169501, ss3649491736, ss3690902546, ss3814099645, ss3845211671, ss3968896464, ss4227558763, ss5285854429, ss5481239919, ss5746489695, ss5811982571, ss5849790845, ss5880980549	NC_000010.11:125841187::TG	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
6110159782	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss39743674	NT_030059.13:78334232::TG	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss81527854, ss95556148	NT_030059.13:78334233::GT	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss4227558764	NC_000010.11:125841187::TGTG	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
6110159782	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
85802677, ss4227558765, ss4870257022	NC_000010.11:125841187::TGTGTGTGTG	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
6110159782	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000010.11:125841187:TGTGTGTGTGT… NC_000010.11:125841187:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(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 rs34263964

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34263964