Name: rs10691267
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.

rs10691267

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:18560097-18560109 (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)₃
Variation Type: Indel Insertion and Deletion
Frequency: dup(GT)₃=0.000170 (45/264690, TOPMED)
(TG)₆T=0.0787 (380/4826, ALFA)
(TG)₆T=0.0049 (22/4480, Estonian) (+ 1 more)
(TG)₆T=0.03 (1/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SEC23B : 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	4826	TGTGTGTGTGTGT=0.0787	TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.9213, TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000	0.073767	0.916287	0.009946	32
European	Sub	4688	TGTGTGTGTGTGT=0.0531	TGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.9469, TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000	0.048208	0.94198	0.009812	32
African	Sub	102	TGTGTGTGTGTGT=1.000	TGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	4	TGTGTGTGTGTGT=1.0	TGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
African American	Sub	98	TGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	TGTGTGTGTGTGT=0	TGTGTGTGTGT=0, TGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
East Asian	Sub	0	TGTGTGTGTGTGT=0	TGTGTGTGTGT=0, TGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
Other Asian	Sub	0	TGTGTGTGTGTGT=0	TGTGTGTGTGT=0, TGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
Latin American 1	Sub	0	TGTGTGTGTGTGT=0	TGTGTGTGTGT=0, TGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
Latin American 2	Sub	16	TGTGTGTGTGTGT=1.00	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	4	TGTGTGTGTGTGT=1.0	TGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Other	Sub	16	TGTGTGTGTGTGT=0.56	TGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.44, TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00	0.5	0.375	0.125	3

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)₃=0.000170
Allele Frequency Aggregator	Total	Global	4826	(TG)₆T=0.0787	delGT=0.0000, dupGT=0.9213, dupGTGT=0.0000, dup(GT)₃=0.0000
Allele Frequency Aggregator	European	Sub	4688	(TG)₆T=0.0531	delGT=0.0000, dupGT=0.9469, dupGTGT=0.0000, dup(GT)₃=0.0000
Allele Frequency Aggregator	African	Sub	102	(TG)₆T=1.000	delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000
Allele Frequency Aggregator	Latin American 2	Sub	16	(TG)₆T=1.00	delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00
Allele Frequency Aggregator	Other	Sub	16	(TG)₆T=0.56	delGT=0.00, dupGT=0.44, dupGTGT=0.00, dup(GT)₃=0.00
Allele Frequency Aggregator	South Asian	Sub	4	(TG)₆T=1.0	delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(TG)₆T=0	delGT=0, dupGT=0, dupGTGT=0, dup(GT)₃=0
Allele Frequency Aggregator	Asian	Sub	0	(TG)₆T=0	delGT=0, dupGT=0, dupGTGT=0, dup(GT)₃=0
Genetic variation in the Estonian population	Estonian	Study-wide	4480	- No frequency provided	dupGT=0.9951
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupGT=0.97

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 20	NC_000020.11:g.18560098GT[5]
GRCh38.p14 chr 20	NC_000020.11:g.18560098GT[7]
GRCh38.p14 chr 20	NC_000020.11:g.18560098GT[8]
GRCh38.p14 chr 20	NC_000020.11:g.18560098GT[9]
GRCh37.p13 chr 20	NC_000020.10:g.18540742GT[5]
GRCh37.p13 chr 20	NC_000020.10:g.18540742GT[7]
GRCh37.p13 chr 20	NC_000020.10:g.18540742GT[8]
GRCh37.p13 chr 20	NC_000020.10:g.18540742GT[9]
SEC23B RefSeqGene (LRG_1134)	NG_016281.2:g.57617GT[5]
SEC23B RefSeqGene (LRG_1134)	NG_016281.2:g.57617GT[7]
SEC23B RefSeqGene (LRG_1134)	NG_016281.2:g.57617GT[8]
SEC23B RefSeqGene (LRG_1134)	NG_016281.2:g.57617GT[9]

Gene: SEC23B, SEC23 homolog B, COPII coat complex component (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SEC23B transcript variant 4	NM_001172745.3:c.2215-554… NM_001172745.3:c.2215-554TG[5]	N/A	Intron Variant
SEC23B transcript variant 5	NM_001172746.3:c.2161-554… NM_001172746.3:c.2161-554TG[5]	N/A	Intron Variant
SEC23B transcript variant 1	NM_006363.6:c.2215-554TG[… NM_006363.6:c.2215-554TG[5]	N/A	Intron Variant
SEC23B transcript variant 2	NM_032985.6:c.2215-554TG[… NM_032985.6:c.2215-554TG[5]	N/A	Intron Variant
SEC23B transcript variant 3	NM_032986.5:c.2215-554TG[… NM_032986.5:c.2215-554TG[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)₃
GRCh38.p14 chr 20	NC_000020.11:g.18560097_18560109=	NC_000020.11:g.18560098GT[5]	NC_000020.11:g.18560098GT[7]	NC_000020.11:g.18560098GT[8]	NC_000020.11:g.18560098GT[9]
GRCh37.p13 chr 20	NC_000020.10:g.18540741_18540753=	NC_000020.10:g.18540742GT[5]	NC_000020.10:g.18540742GT[7]	NC_000020.10:g.18540742GT[8]	NC_000020.10:g.18540742GT[9]
SEC23B RefSeqGene (LRG_1134)	NG_016281.2:g.57616_57628=	NG_016281.2:g.57617GT[5]	NG_016281.2:g.57617GT[7]	NG_016281.2:g.57617GT[8]	NG_016281.2:g.57617GT[9]
SEC23B transcript variant 4	NM_001172745.1:c.2215-554=	NM_001172745.1:c.2215-554TG[5]	NM_001172745.1:c.2215-554TG[7]	NM_001172745.1:c.2215-554TG[8]	NM_001172745.1:c.2215-554TG[9]
SEC23B transcript variant 4	NM_001172745.3:c.2215-554=	NM_001172745.3:c.2215-554TG[5]	NM_001172745.3:c.2215-554TG[7]	NM_001172745.3:c.2215-554TG[8]	NM_001172745.3:c.2215-554TG[9]
SEC23B transcript variant 5	NM_001172746.1:c.2161-554=	NM_001172746.1:c.2161-554TG[5]	NM_001172746.1:c.2161-554TG[7]	NM_001172746.1:c.2161-554TG[8]	NM_001172746.1:c.2161-554TG[9]
SEC23B transcript variant 5	NM_001172746.3:c.2161-554=	NM_001172746.3:c.2161-554TG[5]	NM_001172746.3:c.2161-554TG[7]	NM_001172746.3:c.2161-554TG[8]	NM_001172746.3:c.2161-554TG[9]
SEC23B transcript variant 1	NM_006363.4:c.2215-554=	NM_006363.4:c.2215-554TG[5]	NM_006363.4:c.2215-554TG[7]	NM_006363.4:c.2215-554TG[8]	NM_006363.4:c.2215-554TG[9]
SEC23B transcript variant 1	NM_006363.6:c.2215-554=	NM_006363.6:c.2215-554TG[5]	NM_006363.6:c.2215-554TG[7]	NM_006363.6:c.2215-554TG[8]	NM_006363.6:c.2215-554TG[9]
SEC23B transcript variant 2	NM_032985.4:c.2215-554=	NM_032985.4:c.2215-554TG[5]	NM_032985.4:c.2215-554TG[7]	NM_032985.4:c.2215-554TG[8]	NM_032985.4:c.2215-554TG[9]
SEC23B transcript variant 2	NM_032985.6:c.2215-554=	NM_032985.6:c.2215-554TG[5]	NM_032985.6:c.2215-554TG[7]	NM_032985.6:c.2215-554TG[8]	NM_032985.6:c.2215-554TG[9]
SEC23B transcript variant 3	NM_032986.3:c.2215-554=	NM_032986.3:c.2215-554TG[5]	NM_032986.3:c.2215-554TG[7]	NM_032986.3:c.2215-554TG[8]	NM_032986.3:c.2215-554TG[9]
SEC23B transcript variant 3	NM_032986.5:c.2215-554=	NM_032986.5:c.2215-554TG[5]	NM_032986.5:c.2215-554TG[7]	NM_032986.5:c.2215-554TG[8]	NM_032986.5:c.2215-554TG[9]

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, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41359693	Mar 14, 2006 (126)
2	HGSV	ss82369863	Dec 15, 2007 (130)
3	HUMANGENOME_JCVI	ss95737487	Feb 05, 2009 (130)
4	BUSHMAN	ss193606406	Oct 12, 2018 (152)
5	GMI	ss289405176	May 04, 2012 (138)
6	1000GENOMES	ss327934931	May 09, 2011 (134)
7	1000GENOMES	ss328054761	May 09, 2011 (134)
8	1000GENOMES	ss328291312	May 09, 2011 (134)
9	LUNTER	ss552653527	Apr 25, 2013 (138)
10	LUNTER	ss553050734	Apr 25, 2013 (138)
11	LUNTER	ss553675227	Apr 25, 2013 (138)
12	SSMP	ss664465377	Apr 01, 2015 (144)
13	BILGI_BIOE	ss666741998	Apr 25, 2013 (138)
14	DDI	ss1536904484	Apr 01, 2015 (144)
15	EVA_GENOME_DK	ss1575686962	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1709317582	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1709317583	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1709318223	Apr 01, 2015 (144)
19	EVA_UK10K_TWINSUK	ss1709318224	Apr 01, 2015 (144)
20	GENOMED	ss1969107520	Jul 19, 2016 (147)
21	JJLAB	ss2031425309	Sep 14, 2016 (149)
22	SYSTEMSBIOZJU	ss2629416033	Nov 08, 2017 (151)
23	SWEGEN	ss3017964112	Nov 08, 2017 (151)
24	SWEGEN	ss3017964113	Nov 08, 2017 (151)
25	MCHAISSO	ss3063992372	Nov 08, 2017 (151)
26	MCHAISSO	ss3064849002	Nov 08, 2017 (151)
27	MCHAISSO	ss3065810729	Nov 08, 2017 (151)
28	BEROUKHIMLAB	ss3644444379	Oct 12, 2018 (152)
29	URBANLAB	ss3650985395	Oct 12, 2018 (152)
30	EGCUT_WGS	ss3684686405	Jul 13, 2019 (153)
31	EVA_DECODE	ss3706677825	Jul 13, 2019 (153)
32	EVA_DECODE	ss3706677826	Jul 13, 2019 (153)
33	EVA_DECODE	ss3706677829	Jul 13, 2019 (153)
34	ACPOP	ss3743303249	Jul 13, 2019 (153)
35	ACPOP	ss3743303250	Jul 13, 2019 (153)
36	PACBIO	ss3788616075	Jul 13, 2019 (153)
37	PACBIO	ss3793514021	Jul 13, 2019 (153)
38	PACBIO	ss3798401196	Jul 13, 2019 (153)
39	KHV_HUMAN_GENOMES	ss3821668865	Jul 13, 2019 (153)
40	EVA	ss3835620607	Apr 27, 2020 (154)
41	EVA	ss3846944547	Apr 27, 2020 (154)
42	GNOMAD	ss4336068994	Apr 27, 2021 (155)
43	GNOMAD	ss4336068995	Apr 27, 2021 (155)
44	GNOMAD	ss4336068996	Apr 27, 2021 (155)
45	GNOMAD	ss4336068997	Apr 27, 2021 (155)
46	TOPMED	ss5084324004	Apr 27, 2021 (155)
47	TOMMO_GENOMICS	ss5229103844	Apr 27, 2021 (155)
48	TOMMO_GENOMICS	ss5229103845	Apr 27, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5308290112	Oct 13, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5308290113	Oct 13, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5308290114	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5500673322	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5500673323	Oct 13, 2022 (156)
54	TOMMO_GENOMICS	ss5788164423	Oct 13, 2022 (156)
55	TOMMO_GENOMICS	ss5788164424	Oct 13, 2022 (156)
56	YY_MCH	ss5817869432	Oct 13, 2022 (156)
57	EVA	ss5845528742	Oct 13, 2022 (156)
58	EVA	ss5845528743	Oct 13, 2022 (156)
59	EVA	ss5853095755	Oct 13, 2022 (156)
60	EVA	ss5922913775	Oct 13, 2022 (156)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 43046639 (NC_000020.10:18540740::TG 3764/3854) Row 43046640 (NC_000020.10:18540740::TGTG 50/3854)	-	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 43046639 (NC_000020.10:18540740::TG 3764/3854) Row 43046640 (NC_000020.10:18540740::TGTG 50/3854)	-	Oct 12, 2018 (152)
63	Genetic variation in the Estonian population	NC_000020.10 - 18540741	Oct 12, 2018 (152)
64	The Danish reference pan genome	NC_000020.10 - 18540741	Apr 27, 2020 (154)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548162607 (NC_000020.11:18560096::TG 133678/138172) Row 548162608 (NC_000020.11:18560096::TGTG 933/138176) Row 548162609 (NC_000020.11:18560096::TGTGTG 13/138184)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548162607 (NC_000020.11:18560096::TG 133678/138172) Row 548162608 (NC_000020.11:18560096::TGTG 933/138176) Row 548162609 (NC_000020.11:18560096::TGTGTG 13/138184)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548162607 (NC_000020.11:18560096::TG 133678/138172) Row 548162608 (NC_000020.11:18560096::TGTG 933/138176) Row 548162609 (NC_000020.11:18560096::TGTGTG 13/138184)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 548162607 (NC_000020.11:18560096::TG 133678/138172) Row 548162608 (NC_000020.11:18560096::TGTG 933/138176) Row 548162609 (NC_000020.11:18560096::TGTGTG 13/138184)...	-	Apr 27, 2021 (155)
69	Northern Sweden Submission ignored due to conflicting rows: Row 16588114 (NC_000020.10:18540740::TG 589/600) Row 16588115 (NC_000020.10:18540740::TGTG 5/600)	-	Jul 13, 2019 (153)
70	Northern Sweden Submission ignored due to conflicting rows: Row 16588114 (NC_000020.10:18540740::TG 589/600) Row 16588115 (NC_000020.10:18540740::TGTG 5/600)	-	Jul 13, 2019 (153)
71	8.3KJPN Submission ignored due to conflicting rows: Row 87073151 (NC_000020.10:18540740::TG 16328/16760) Row 87073152 (NC_000020.10:18540740::TGTG 8/16760)	-	Apr 27, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 87073151 (NC_000020.10:18540740::TG 16328/16760) Row 87073152 (NC_000020.10:18540740::TGTG 8/16760)	-	Apr 27, 2021 (155)
73	14KJPN Submission ignored due to conflicting rows: Row 122001527 (NC_000020.11:18560096::TG 27544/28258) Row 122001528 (NC_000020.11:18560096::TGTG 19/28258)	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 122001527 (NC_000020.11:18560096::TG 27544/28258) Row 122001528 (NC_000020.11:18560096::TGTG 19/28258)	-	Oct 13, 2022 (156)
75	TopMed	NC_000020.11 - 18560097	Apr 27, 2021 (155)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43046639 (NC_000020.10:18540740::TG 3620/3708) Row 43046640 (NC_000020.10:18540740::TGTG 58/3708)	-	Oct 12, 2018 (152)
77	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43046639 (NC_000020.10:18540740::TG 3620/3708) Row 43046640 (NC_000020.10:18540740::TGTG 58/3708)	-	Oct 12, 2018 (152)
78	ALFA	NC_000020.11 - 18560097	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).

Associated ID	History Updated (Build)
rs58738147	May 25, 2008 (130)
rs200410819	Apr 25, 2013 (138)
rs906625949	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4336068997, ss5308290113	NC_000020.11:18560096:TG:	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGT	(self)
11100824206	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGT	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGT	(self)
ss327934931, ss328054761, ss328291312, ss552653527, ss553050734, ss553675227	NC_000020.9:18488740::TG	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss289405176	NC_000020.9:18488753::GT	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
30424653, 752574, ss664465377, ss666741998, ss1536904484, ss1575686962, ss1709317582, ss1709318223, ss1969107520, ss2031425309, ss2629416033, ss3017964112, ss3644444379, ss3684686405, ss3743303249, ss3788616075, ss3793514021, ss3798401196, ss3835620607, ss5229103844, ss5845528742	NC_000020.10:18540740::TG	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss3063992372, ss3064849002, ss3065810729, ss3650985395, ss3706677825, ss3821668865, ss3846944547, ss4336068994, ss5308290112, ss5500673322, ss5788164423, ss5817869432, ss5853095755, ss5922913775	NC_000020.11:18560096::TG	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
11100824206	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss41359693, ss82369863, ss95737487	NT_011387.8:18480753::GT	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss193606406	NT_011387.9:18500097::GT	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss1709317583, ss1709318224, ss3017964113, ss3743303250, ss5229103845, ss5845528743	NC_000020.10:18540740::TGTG	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
ss3706677826, ss4336068995, ss5308290114, ss5500673323, ss5788164424	NC_000020.11:18560096::TGTG	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
11100824206	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
ss3706677829	NC_000020.11:18560108::TGTG	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
359432949, ss4336068996, ss5084324004	NC_000020.11:18560096::TGTGTG	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
11100824206	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	NC_000020.11:18560096:TGTGTGTGTGTG… NC_000020.11:18560096:TGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(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 rs10691267

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

rs10691267