Name: rs63305862
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.

rs63305862

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:111105151-111105160 (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: delTT / delT / dupT / dupTT
Variation Type: Indel Insertion and Deletion
Frequency: (T)₁₀=0.10431 (2620/25118, 14KJPN)
(T)₁₀=0.08562 (1435/16760, 8.3KJPN)
(T)₁₀=0.2679 (1388/5182, ALFA) (+ 5 more)
(T)₁₀=0.2240 (1120/4999, 1000G)
(T)₁₀=0.0618 (238/3854, ALSPAC)
(T)₁₀=0.0599 (222/3708, TWINSUK)
(T)₁₀=0.075 (45/600, NorthernSweden)
(T)₁₀=0.07 (3/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NECTIN3 : 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	5182	TTTTTTTTTT=0.2679	TTTTTTTT=0.0000, TTTTTTTTT=0.7321, TTTTTTTTTTT=0.0000	0.175681	0.630872	0.193447	32
European	Sub	4360	TTTTTTTTTT=0.1314	TTTTTTTT=0.0000, TTTTTTTTT=0.8686, TTTTTTTTTTT=0.0000	0.017908	0.751649	0.230443	0
African	Sub	760	TTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	38	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	722	TTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	10	TTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	18	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	34	TTTTTTTTTT=0.79	TTTTTTTT=0.00, TTTTTTTTT=0.21, TTTTTTTTTTT=0.00	0.764706	0.176471	0.058824	7

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
14KJPN	JAPANESE	Study-wide	25118	(T)₁₀=0.10431	delT=0.89569
8.3KJPN	JAPANESE	Study-wide	16760	(T)₁₀=0.08562	delT=0.91438
Allele Frequency Aggregator	Total	Global	5182	(T)₁₀=0.2679	delTT=0.0000, delT=0.7321, dupT=0.0000
Allele Frequency Aggregator	European	Sub	4360	(T)₁₀=0.1314	delTT=0.0000, delT=0.8686, dupT=0.0000
Allele Frequency Aggregator	African	Sub	760	(T)₁₀=1.000	delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Other	Sub	34	(T)₁₀=0.79	delTT=0.00, delT=0.21, dupT=0.00
Allele Frequency Aggregator	Latin American 2	Sub	18	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	10	(T)₁₀=1.0	delTT=0.0, delT=0.0, dupT=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₁₀=0	delTT=0, delT=0, dupT=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₁₀=0	delTT=0, delT=0, dupT=0
1000Genomes	Global	Study-wide	4999	(T)₁₀=0.2240	delT=0.7760
1000Genomes	African	Sub	1315	(T)₁₀=0.5909	delT=0.4091
1000Genomes	East Asian	Sub	1007	(T)₁₀=0.0983	delT=0.9017
1000Genomes	Europe	Sub	1005	(T)₁₀=0.0697	delT=0.9303
1000Genomes	South Asian	Sub	978	(T)₁₀=0.053	delT=0.947
1000Genomes	American	Sub	694	(T)₁₀=0.176	delT=0.824
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₀=0.0618	delT=0.9382
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(T)₁₀=0.0599	delT=0.9401
Northern Sweden	ACPOP	Study-wide	600	(T)₁₀=0.075	delT=0.925
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₀=0.07	delT=0.93

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 3	NC_000003.12:g.111105159_111105160del
GRCh38.p14 chr 3	NC_000003.12:g.111105160del
GRCh38.p14 chr 3	NC_000003.12:g.111105160dup
GRCh38.p14 chr 3	NC_000003.12:g.111105159_111105160dup
GRCh37.p13 chr 3	NC_000003.11:g.110824006_110824007del
GRCh37.p13 chr 3	NC_000003.11:g.110824007del
GRCh37.p13 chr 3	NC_000003.11:g.110824007dup
GRCh37.p13 chr 3	NC_000003.11:g.110824006_110824007dup
NECTIN3 RefSeqGene	NG_029835.1:g.38401_38402del
NECTIN3 RefSeqGene	NG_029835.1:g.38402del
NECTIN3 RefSeqGene	NG_029835.1:g.38402dup
NECTIN3 RefSeqGene	NG_029835.1:g.38401_38402dup

Gene: NECTIN3, nectin cell adhesion molecule 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NECTIN3 transcript variant 2	NM_001243286.2:c.161-6871… NM_001243286.2:c.161-6871_161-6870del	N/A	Intron Variant
NECTIN3 transcript variant 3	NM_001243288.2:c.92-6871_… NM_001243288.2:c.92-6871_92-6870del	N/A	Intron Variant
NECTIN3 transcript variant 1	NM_015480.3:c.161-6871_16… NM_015480.3:c.161-6871_161-6870del	N/A	Intron Variant
NECTIN3 transcript variant X1	XM_011512663.2:c.254-6871… XM_011512663.2:c.254-6871_254-6870del	N/A	Intron Variant
NECTIN3 transcript variant X2	XM_017006123.2:c.254-6871… XM_017006123.2:c.254-6871_254-6870del	N/A	Intron Variant
NECTIN3 transcript variant X3	XM_017006124.2:c.116-6871… XM_017006124.2:c.116-6871_116-6870del	N/A	Intron Variant
NECTIN3 transcript variant X4	XM_017006125.2:c.92-6871_… XM_017006125.2:c.92-6871_92-6870del	N/A	Intron Variant
NECTIN3 transcript variant X5	XM_017006126.2:c.161-6871… XM_017006126.2:c.161-6871_161-6870del	N/A	Intron Variant
NECTIN3 transcript variant X7	XM_017006127.3:c.-476-687… XM_017006127.3:c.-476-6871_-476-6870del	N/A	Intron Variant
NECTIN3 transcript variant X6	XM_047447934.1:c.-476-687… XM_047447934.1:c.-476-6871_-476-6870del	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	(T)₁₀=	delTT	delT	dupT	dupTT
GRCh38.p14 chr 3	NC_000003.12:g.111105151_111105160=	NC_000003.12:g.111105159_111105160del	NC_000003.12:g.111105160del	NC_000003.12:g.111105160dup	NC_000003.12:g.111105159_111105160dup
GRCh37.p13 chr 3	NC_000003.11:g.110823998_110824007=	NC_000003.11:g.110824006_110824007del	NC_000003.11:g.110824007del	NC_000003.11:g.110824007dup	NC_000003.11:g.110824006_110824007dup
NECTIN3 RefSeqGene	NG_029835.1:g.38393_38402=	NG_029835.1:g.38401_38402del	NG_029835.1:g.38402del	NG_029835.1:g.38402dup	NG_029835.1:g.38401_38402dup
NECTIN3 transcript variant 2	NM_001243286.1:c.161-6879=	NM_001243286.1:c.161-6871_161-6870del	NM_001243286.1:c.161-6870del	NM_001243286.1:c.161-6870dup	NM_001243286.1:c.161-6871_161-6870dup
NECTIN3 transcript variant 2	NM_001243286.2:c.161-6879=	NM_001243286.2:c.161-6871_161-6870del	NM_001243286.2:c.161-6870del	NM_001243286.2:c.161-6870dup	NM_001243286.2:c.161-6871_161-6870dup
NECTIN3 transcript variant 3	NM_001243288.1:c.92-6879=	NM_001243288.1:c.92-6871_92-6870del	NM_001243288.1:c.92-6870del	NM_001243288.1:c.92-6870dup	NM_001243288.1:c.92-6871_92-6870dup
NECTIN3 transcript variant 3	NM_001243288.2:c.92-6879=	NM_001243288.2:c.92-6871_92-6870del	NM_001243288.2:c.92-6870del	NM_001243288.2:c.92-6870dup	NM_001243288.2:c.92-6871_92-6870dup
NECTIN3 transcript variant 1	NM_015480.2:c.161-6879=	NM_015480.2:c.161-6871_161-6870del	NM_015480.2:c.161-6870del	NM_015480.2:c.161-6870dup	NM_015480.2:c.161-6871_161-6870dup
NECTIN3 transcript variant 1	NM_015480.3:c.161-6879=	NM_015480.3:c.161-6871_161-6870del	NM_015480.3:c.161-6870del	NM_015480.3:c.161-6870dup	NM_015480.3:c.161-6871_161-6870dup
PVRL3 transcript variant X1	XM_005247321.1:c.92-6879=	XM_005247321.1:c.92-6871_92-6870del	XM_005247321.1:c.92-6870del	XM_005247321.1:c.92-6870dup	XM_005247321.1:c.92-6871_92-6870dup
PVRL3 transcript variant X2	XM_005247322.1:c.161-6879=	XM_005247322.1:c.161-6871_161-6870del	XM_005247322.1:c.161-6870del	XM_005247322.1:c.161-6870dup	XM_005247322.1:c.161-6871_161-6870dup
NECTIN3 transcript variant X1	XM_011512663.2:c.254-6879=	XM_011512663.2:c.254-6871_254-6870del	XM_011512663.2:c.254-6870del	XM_011512663.2:c.254-6870dup	XM_011512663.2:c.254-6871_254-6870dup
NECTIN3 transcript variant X2	XM_017006123.2:c.254-6879=	XM_017006123.2:c.254-6871_254-6870del	XM_017006123.2:c.254-6870del	XM_017006123.2:c.254-6870dup	XM_017006123.2:c.254-6871_254-6870dup
NECTIN3 transcript variant X3	XM_017006124.2:c.116-6879=	XM_017006124.2:c.116-6871_116-6870del	XM_017006124.2:c.116-6870del	XM_017006124.2:c.116-6870dup	XM_017006124.2:c.116-6871_116-6870dup
NECTIN3 transcript variant X4	XM_017006125.2:c.92-6879=	XM_017006125.2:c.92-6871_92-6870del	XM_017006125.2:c.92-6870del	XM_017006125.2:c.92-6870dup	XM_017006125.2:c.92-6871_92-6870dup
NECTIN3 transcript variant X5	XM_017006126.2:c.161-6879=	XM_017006126.2:c.161-6871_161-6870del	XM_017006126.2:c.161-6870del	XM_017006126.2:c.161-6870dup	XM_017006126.2:c.161-6871_161-6870dup
NECTIN3 transcript variant X7	XM_017006127.3:c.-476-6879=	XM_017006127.3:c.-476-6871_-476-6870del	XM_017006127.3:c.-476-6870del	XM_017006127.3:c.-476-6870dup	XM_017006127.3:c.-476-6871_-476-6870dup
NECTIN3 transcript variant X6	XM_047447934.1:c.-476-6879=	XM_047447934.1:c.-476-6871_-476-6870del	XM_047447934.1:c.-476-6870del	XM_047447934.1:c.-476-6870dup	XM_047447934.1:c.-476-6871_-476-6870dup

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#.

54 SubSNP, 12 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95328028	Dec 05, 2013 (138)
2	GMI	ss287731470	May 09, 2011 (137)
3	GMI	ss288400593	May 04, 2012 (137)
4	PJP	ss295118783	May 09, 2011 (137)
5	PJP	ss295118784	May 09, 2011 (134)
6	1000GENOMES	ss326411173	May 09, 2011 (137)
7	1000GENOMES	ss326433643	May 09, 2011 (137)
8	1000GENOMES	ss326562942	May 09, 2011 (137)
9	1000GENOMES	ss499873724	May 04, 2012 (137)
10	LUNTER	ss551267479	Apr 25, 2013 (138)
11	LUNTER	ss551362394	Apr 25, 2013 (138)
12	LUNTER	ss553049365	Apr 25, 2013 (138)
13	SSMP	ss663344227	Apr 01, 2015 (144)
14	BILGI_BIOE	ss666221764	Apr 25, 2013 (138)
15	1000GENOMES	ss1370805403	Aug 21, 2014 (142)
16	1000GENOMES	ss1370805406	Oct 12, 2018 (152)
17	DDI	ss1536367334	Apr 01, 2015 (144)
18	EVA_GENOME_DK	ss1576011078	Apr 01, 2015 (144)
19	EVA_UK10K_ALSPAC	ss1703770432	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1703770481	Apr 01, 2015 (144)
21	HAMMER_LAB	ss1799846878	Sep 08, 2015 (146)
22	JJLAB	ss2030535435	Sep 14, 2016 (149)
23	SYSTEMSBIOZJU	ss2625345324	Nov 08, 2017 (151)
24	AFFY	ss2985886996	Nov 08, 2017 (151)
25	SWEGEN	ss2992970255	Nov 08, 2017 (151)
26	MCHAISSO	ss3064062779	Nov 08, 2017 (151)
27	MCHAISSO	ss3064925031	Nov 08, 2017 (151)
28	MCHAISSO	ss3065898825	Nov 08, 2017 (151)
29	BEROUKHIMLAB	ss3644133084	Oct 12, 2018 (152)
30	BIOINF_KMB_FNS_UNIBA	ss3645735024	Oct 12, 2018 (152)
31	URBANLAB	ss3647496305	Oct 12, 2018 (152)
32	EVA_DECODE	ss3710017790	Jul 13, 2019 (153)
33	ACPOP	ss3730228183	Jul 13, 2019 (153)
34	PACBIO	ss3784424716	Jul 13, 2019 (153)
35	PACBIO	ss3789925342	Jul 13, 2019 (153)
36	PACBIO	ss3794799760	Jul 13, 2019 (153)
37	EVA	ss3828004113	Apr 25, 2020 (154)
38	EVA	ss3837433917	Apr 25, 2020 (154)
39	EVA	ss3842863735	Apr 25, 2020 (154)
40	GNOMAD	ss4078400724	Apr 26, 2021 (155)
41	GNOMAD	ss4078400725	Apr 26, 2021 (155)
42	GNOMAD	ss4078400727	Apr 26, 2021 (155)
43	GNOMAD	ss4078400728	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5160957086	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5255548149	Oct 12, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5255548150	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5454743206	Oct 12, 2022 (156)
48	TOMMO_GENOMICS	ss5693652479	Oct 12, 2022 (156)
49	YY_MCH	ss5804122922	Oct 12, 2022 (156)
50	EVA	ss5826293307	Oct 12, 2022 (156)
51	EVA	ss5853777409	Oct 12, 2022 (156)
52	EVA	ss5870448881	Oct 12, 2022 (156)
53	EVA	ss5961250595	Oct 12, 2022 (156)
54	EVA	ss5980165130	Oct 12, 2022 (156)
55	1000Genomes	NC_000003.11 - 110823998	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children	NC_000003.11 - 110823998	Oct 12, 2018 (152)
57	The Danish reference pan genome	NC_000003.11 - 110823998	Apr 25, 2020 (154)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 119780927 (NC_000003.12:111105150::T 137/122712) Row 119780928 (NC_000003.12:111105150::TT 1/122720) Row 119780930 (NC_000003.12:111105150:T: 94421/123482)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 119780927 (NC_000003.12:111105150::T 137/122712) Row 119780928 (NC_000003.12:111105150::TT 1/122720) Row 119780930 (NC_000003.12:111105150:T: 94421/123482)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 119780927 (NC_000003.12:111105150::T 137/122712) Row 119780928 (NC_000003.12:111105150::TT 1/122720) Row 119780930 (NC_000003.12:111105150:T: 94421/123482)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 119780927 (NC_000003.12:111105150::T 137/122712) Row 119780928 (NC_000003.12:111105150::TT 1/122720) Row 119780930 (NC_000003.12:111105150:T: 94421/123482)...	-	Apr 26, 2021 (155)
62	Northern Sweden	NC_000003.11 - 110823998	Jul 13, 2019 (153)
63	8.3KJPN	NC_000003.11 - 110823998	Apr 26, 2021 (155)
64	14KJPN	NC_000003.12 - 111105151	Oct 12, 2022 (156)
65	UK 10K study - Twins	NC_000003.11 - 110823998	Oct 12, 2018 (152)
66	ALFA	NC_000003.12 - 111105151	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)
rs140298087	May 11, 2012 (137)
rs147915053	May 04, 2012 (137)
rs367866511	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4078400728	NC_000003.12:111105150:TT:	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTT	(self)
908047327	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTT	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTT	(self)
ss288400593, ss295118783, ss326411173, ss326433643, ss326562942, ss551267479, ss551362394, ss553049365	NC_000003.10:112306687:T:	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTT	(self)
ss295118784	NC_000003.10:112306696:T:	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTT	(self)
16843949, 9374350, 847883, 3513048, 18926393, 9374350, ss499873724, ss663344227, ss666221764, ss1370805403, ss1536367334, ss1576011078, ss1703770432, ss1703770481, ss1799846878, ss2030535435, ss2625345324, ss2985886996, ss2992970255, ss3644133084, ss3730228183, ss3784424716, ss3789925342, ss3794799760, ss3828004113, ss3837433917, ss5160957086, ss5826293307, ss5961250595, ss5980165130	NC_000003.11:110823997:T:	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTT	(self)
27489583, ss3064062779, ss3064925031, ss3065898825, ss3645735024, ss3647496305, ss3710017790, ss3842863735, ss4078400727, ss5255548149, ss5454743206, ss5693652479, ss5804122922, ss5853777409, ss5870448881	NC_000003.12:111105150:T:	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTT	(self)
908047327	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTT	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTT	(self)
ss287731470	NT_005612.16:17319143:T:	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTT	(self)
ss95328028	NT_005612.16:17319152:T:	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTT	(self)
ss1370805406	NC_000003.11:110823998::T	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss4078400724, ss5255548150	NC_000003.12:111105150::T	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTTTT	(self)
908047327	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTTTT	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss4078400725	NC_000003.12:111105150::TT	NC_000003.12:111105150:TTTTTTTTTT:… NC_000003.12:111105150:TTTTTTTTTT:TTTTTTTTTTTT	(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 rs63305862

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

rs63305862