Name: rs149478337
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.

rs149478337

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:125044451-125044467 (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: del(T)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.06494 (678/10440, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BRI3BP : 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	10440	TTTTTTTTTTTTTTTTT=0.88525	TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.04981, TTTTTTTTTTTTTTTTTT=0.06494, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000	0.893559	0.020275	0.086167	32
European	Sub	8244	TTTTTTTTTTTTTTTTT=0.8548	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0631, TTTTTTTTTTTTTTTTTT=0.0821, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	0.861699	0.026395	0.111905	32
African	Sub	1586	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	68	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1518	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	40	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	30	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	68	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	226	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	30	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	246	TTTTTTTTTTTTTTTTT=0.996	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.004, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	0.99187	0.0	0.00813	0

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
Allele Frequency Aggregator	Total	Global	10440	(T)₁₇=0.88525	del(T)₄=0.00000, delTT=0.00000, delT=0.04981, dupT=0.06494, dupTT=0.00000, dupTTT=0.00000
Allele Frequency Aggregator	European	Sub	8244	(T)₁₇=0.8548	del(T)₄=0.0000, delTT=0.0000, delT=0.0631, dupT=0.0821, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	1586	(T)₁₇=1.0000	del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Other	Sub	246	(T)₁₇=0.996	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.004, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	226	(T)₁₇=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	68	(T)₁₇=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	40	(T)₁₇=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(T)₁₇=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00

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 12	NC_000012.12:g.125044464_125044467del
GRCh38.p14 chr 12	NC_000012.12:g.125044465_125044467del
GRCh38.p14 chr 12	NC_000012.12:g.125044466_125044467del
GRCh38.p14 chr 12	NC_000012.12:g.125044467del
GRCh38.p14 chr 12	NC_000012.12:g.125044467dup
GRCh38.p14 chr 12	NC_000012.12:g.125044466_125044467dup
GRCh38.p14 chr 12	NC_000012.12:g.125044465_125044467dup
GRCh38.p14 chr 12	NC_000012.12:g.125044460_125044467dup
GRCh37.p13 chr 12	NC_000012.11:g.125529010_125529013del
GRCh37.p13 chr 12	NC_000012.11:g.125529011_125529013del
GRCh37.p13 chr 12	NC_000012.11:g.125529012_125529013del
GRCh37.p13 chr 12	NC_000012.11:g.125529013del
GRCh37.p13 chr 12	NC_000012.11:g.125529013dup
GRCh37.p13 chr 12	NC_000012.11:g.125529012_125529013dup
GRCh37.p13 chr 12	NC_000012.11:g.125529011_125529013dup
GRCh37.p13 chr 12	NC_000012.11:g.125529006_125529013dup

Gene: BRI3BP, BRI3 binding protein (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BRI3BP transcript	NM_080626.6:c.	N/A	Genic Downstream Transcript Variant
BRI3BP transcript variant X1	XM_011537940.3:c.317-6498… XM_011537940.3:c.317-6498_317-6495del	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)₁₇=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₈
GRCh38.p14 chr 12	NC_000012.12:g.125044451_125044467=	NC_000012.12:g.125044464_125044467del	NC_000012.12:g.125044465_125044467del	NC_000012.12:g.125044466_125044467del	NC_000012.12:g.125044467del	NC_000012.12:g.125044467dup	NC_000012.12:g.125044466_125044467dup	NC_000012.12:g.125044465_125044467dup	NC_000012.12:g.125044460_125044467dup
GRCh37.p13 chr 12	NC_000012.11:g.125528997_125529013=	NC_000012.11:g.125529010_125529013del	NC_000012.11:g.125529011_125529013del	NC_000012.11:g.125529012_125529013del	NC_000012.11:g.125529013del	NC_000012.11:g.125529013dup	NC_000012.11:g.125529012_125529013dup	NC_000012.11:g.125529011_125529013dup	NC_000012.11:g.125529006_125529013dup
BRI3BP transcript variant X1	XM_011537940.3:c.317-6511=	XM_011537940.3:c.317-6498_317-6495del	XM_011537940.3:c.317-6497_317-6495del	XM_011537940.3:c.317-6496_317-6495del	XM_011537940.3:c.317-6495del	XM_011537940.3:c.317-6495dup	XM_011537940.3:c.317-6496_317-6495dup	XM_011537940.3:c.317-6497_317-6495dup	XM_011537940.3:c.317-6502_317-6495dup

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#.

35 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss294780435	May 09, 2011 (134)
2	SSMP	ss664098741	Apr 01, 2015 (144)
3	SSIP	ss947308365	Oct 12, 2018 (152)
4	SWEGEN	ss3010516654	Nov 08, 2017 (151)
5	URBANLAB	ss3649942444	Oct 12, 2018 (152)
6	EVA_DECODE	ss3694675858	Jul 13, 2019 (153)
7	EVA_DECODE	ss3694675859	Jul 13, 2019 (153)
8	EVA_DECODE	ss3694675860	Jul 13, 2019 (153)
9	EVA_DECODE	ss3694675861	Jul 13, 2019 (153)
10	ACPOP	ss3739470448	Jul 13, 2019 (153)
11	ACPOP	ss3739470449	Jul 13, 2019 (153)
12	EVA	ss3833378976	Apr 27, 2020 (154)
13	KOGIC	ss3972955867	Apr 27, 2020 (154)
14	KOGIC	ss3972955868	Apr 27, 2020 (154)
15	KOGIC	ss3972955869	Apr 27, 2020 (154)
16	GNOMAD	ss4260807040	Apr 26, 2021 (155)
17	GNOMAD	ss4260807041	Apr 26, 2021 (155)
18	GNOMAD	ss4260807042	Apr 26, 2021 (155)
19	GNOMAD	ss4260807044	Apr 26, 2021 (155)
20	GNOMAD	ss4260807045	Apr 26, 2021 (155)
21	GNOMAD	ss4260807046	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5208646496	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5208646497	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5208646498	Apr 26, 2021 (155)
25	1000G_HIGH_COVERAGE	ss5292595677	Oct 16, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5292595678	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5292595679	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5292595681	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5487161275	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5487161276	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5487161277	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5759123894	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5759123895	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5759123896	Oct 16, 2022 (156)
35	EVA	ss5850591907	Oct 16, 2022 (156)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 422279068 (NC_000012.12:125044450::T 22047/127082) Row 422279069 (NC_000012.12:125044450::TT 85/127160) Row 422279070 (NC_000012.12:125044450::TTT 4/127174)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 422279068 (NC_000012.12:125044450::T 22047/127082) Row 422279069 (NC_000012.12:125044450::TT 85/127160) Row 422279070 (NC_000012.12:125044450::TTT 4/127174)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 422279068 (NC_000012.12:125044450::T 22047/127082) Row 422279069 (NC_000012.12:125044450::TT 85/127160) Row 422279070 (NC_000012.12:125044450::TTT 4/127174)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 422279068 (NC_000012.12:125044450::T 22047/127082) Row 422279069 (NC_000012.12:125044450::TT 85/127160) Row 422279070 (NC_000012.12:125044450::TTT 4/127174)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 422279068 (NC_000012.12:125044450::T 22047/127082) Row 422279069 (NC_000012.12:125044450::TT 85/127160) Row 422279070 (NC_000012.12:125044450::TTT 4/127174)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 422279068 (NC_000012.12:125044450::T 22047/127082) Row 422279069 (NC_000012.12:125044450::TT 85/127160) Row 422279070 (NC_000012.12:125044450::TTT 4/127174)...	-	Apr 26, 2021 (155)
42	Korean Genome Project Submission ignored due to conflicting rows: Row 29333868 (NC_000012.12:125044452::T 262/1832) Row 29333869 (NC_000012.12:125044450:TT: 24/1832) Row 29333870 (NC_000012.12:125044451:T: 599/1832)	-	Apr 27, 2020 (154)
43	Korean Genome Project Submission ignored due to conflicting rows: Row 29333868 (NC_000012.12:125044452::T 262/1832) Row 29333869 (NC_000012.12:125044450:TT: 24/1832) Row 29333870 (NC_000012.12:125044451:T: 599/1832)	-	Apr 27, 2020 (154)
44	Korean Genome Project Submission ignored due to conflicting rows: Row 29333868 (NC_000012.12:125044452::T 262/1832) Row 29333869 (NC_000012.12:125044450:TT: 24/1832) Row 29333870 (NC_000012.12:125044451:T: 599/1832)	-	Apr 27, 2020 (154)
45	Northern Sweden Submission ignored due to conflicting rows: Row 12755313 (NC_000012.11:125528996:T: 71/598) Row 12755314 (NC_000012.11:125528996::T 67/598)	-	Jul 13, 2019 (153)
46	Northern Sweden Submission ignored due to conflicting rows: Row 12755313 (NC_000012.11:125528996:T: 71/598) Row 12755314 (NC_000012.11:125528996::T 67/598)	-	Jul 13, 2019 (153)
47	8.3KJPN Submission ignored due to conflicting rows: Row 66615803 (NC_000012.11:125528996:T: 4691/16742) Row 66615804 (NC_000012.11:125528996::T 2578/16742) Row 66615805 (NC_000012.11:125528996::TT 8/16742)	-	Apr 26, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 66615803 (NC_000012.11:125528996:T: 4691/16742) Row 66615804 (NC_000012.11:125528996::T 2578/16742) Row 66615805 (NC_000012.11:125528996::TT 8/16742)	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 66615803 (NC_000012.11:125528996:T: 4691/16742) Row 66615804 (NC_000012.11:125528996::T 2578/16742) Row 66615805 (NC_000012.11:125528996::TT 8/16742)	-	Apr 26, 2021 (155)
50	14KJPN Submission ignored due to conflicting rows: Row 92960998 (NC_000012.12:125044450::T 4202/28254) Row 92960999 (NC_000012.12:125044450:T: 8164/28254) Row 92961000 (NC_000012.12:125044450::TT 10/28254)	-	Oct 16, 2022 (156)
51	14KJPN Submission ignored due to conflicting rows: Row 92960998 (NC_000012.12:125044450::T 4202/28254) Row 92960999 (NC_000012.12:125044450:T: 8164/28254) Row 92961000 (NC_000012.12:125044450::TT 10/28254)	-	Oct 16, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 92960998 (NC_000012.12:125044450::T 4202/28254) Row 92960999 (NC_000012.12:125044450:T: 8164/28254) Row 92961000 (NC_000012.12:125044450::TT 10/28254)	-	Oct 16, 2022 (156)
53	ALFA	NC_000012.12 - 125044451	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
828112151	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4260807046	NC_000012.12:125044450:TTT:	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3694675858, ss3972955868, ss4260807045, ss5292595681, ss5487161277	NC_000012.12:125044450:TT:	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
828112151	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss294780435	NC_000012.10:124094965:T:	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss664098741, ss3010516654, ss3739470448, ss5208646496	NC_000012.11:125528996:T:	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4260807044, ss5292595678, ss5487161276, ss5759123895, ss5850591907	NC_000012.12:125044450:T:	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
828112151	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3694675859, ss3972955869	NC_000012.12:125044451:T:	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3739470449, ss3833378976, ss5208646497	NC_000012.11:125528996::T	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss947308365	NC_000012.11:125528997::T	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3649942444, ss4260807040, ss5292595677, ss5487161275, ss5759123894	NC_000012.12:125044450::T	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
828112151	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3694675860, ss3972955867	NC_000012.12:125044452::T	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5208646498	NC_000012.11:125528996::TT	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4260807041, ss5292595679, ss5759123896	NC_000012.12:125044450::TT	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
828112151	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4260807042	NC_000012.12:125044450::TTT	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
828112151	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3694675861	NC_000012.12:125044452::TTTTTTTT	NC_000012.12:125044450:TTTTTTTTTTT… NC_000012.12:125044450:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs149478337

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

rs149478337