Name: rs3832965
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.

rs3832965

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:76446370-76446381 (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: delTTT / delTT / delT / dupT / dup…
delTTT / delTT / delT / dupT / dupTT
Variation Type: Indel Insertion and Deletion
Frequency: delTTT=0.0000 (0/5198, ALFA)
delTT=0.0000 (0/5198, ALFA)
delT=0.0000 (0/5198, ALFA) (+ 3 more)
dupT=0.0000 (0/5198, ALFA)
dupTT=0.0000 (0/5198, ALFA)
delTTT=0.1873 (938/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ESRRB : 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	HWEP
Total	Global	5198	TTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	3790	TTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	718	TTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	N/A
African Others	Sub	20	TTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	698	TTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	N/A
Asian	Sub	50	TTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	36	TTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	14	TTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	68	TTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	304	TTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	60	TTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	208	TTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000	1.0	N/A

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	5198	(T)₁₂=1.0000	delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	3790	(T)₁₂=1.0000	delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	718	(T)₁₂=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	304	(T)₁₂=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	208	(T)₁₂=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	68	(T)₁₂=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	60	(T)₁₂=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	50	(T)₁₂=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₂=0.8127	delTTT=0.1873
1000Genomes	African	Sub	1322	(T)₁₂=0.8638	delTTT=0.1362
1000Genomes	East Asian	Sub	1008	(T)₁₂=0.8631	delTTT=0.1369
1000Genomes	Europe	Sub	1006	(T)₁₂=0.6928	delTTT=0.3072
1000Genomes	South Asian	Sub	978	(T)₁₂=0.863	delTTT=0.137
1000Genomes	American	Sub	694	(T)₁₂=0.745	delTTT=0.255

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 14	NC_000014.9:g.76446379_76446381del
GRCh38.p14 chr 14	NC_000014.9:g.76446380_76446381del
GRCh38.p14 chr 14	NC_000014.9:g.76446381del
GRCh38.p14 chr 14	NC_000014.9:g.76446381dup
GRCh38.p14 chr 14	NC_000014.9:g.76446380_76446381dup
GRCh37.p13 chr 14	NC_000014.8:g.76912722_76912724del
GRCh37.p13 chr 14	NC_000014.8:g.76912723_76912724del
GRCh37.p13 chr 14	NC_000014.8:g.76912724del
GRCh37.p13 chr 14	NC_000014.8:g.76912724dup
GRCh37.p13 chr 14	NC_000014.8:g.76912723_76912724dup
ESRRB RefSeqGene	NG_012278.2:g.80033_80035del
ESRRB RefSeqGene	NG_012278.2:g.80034_80035del
ESRRB RefSeqGene	NG_012278.2:g.80035del
ESRRB RefSeqGene	NG_012278.2:g.80035dup
ESRRB RefSeqGene	NG_012278.2:g.80034_80035dup

Gene: ESRRB, estrogen related receptor beta (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ESRRB transcript variant 2	NM_001379180.1:c.460+6629… NM_001379180.1:c.460+6629_460+6631del	N/A	Intron Variant
ESRRB transcript variant 1	NM_004452.4:c.397+6629_39… NM_004452.4:c.397+6629_397+6631del	N/A	Intron Variant
ESRRB transcript variant X1	XM_011536547.3:c.460+6629… XM_011536547.3:c.460+6629_460+6631del	N/A	Intron Variant
ESRRB transcript variant X3	XM_011536550.3:c.397+6629… XM_011536550.3:c.397+6629_397+6631del	N/A	Intron Variant
ESRRB transcript variant X4	XM_011536553.3:c.460+6629… XM_011536553.3:c.460+6629_460+6631del	N/A	Intron Variant
ESRRB transcript variant X5	XM_011536554.3:c.460+6629… XM_011536554.3:c.460+6629_460+6631del	N/A	Intron Variant
ESRRB transcript variant X6	XM_024449508.2:c.460+6629… XM_024449508.2:c.460+6629_460+6631del	N/A	Intron Variant
ESRRB transcript variant X2	XM_047431079.1:c.397+6629… XM_047431079.1:c.397+6629_397+6631del	N/A	Intron Variant
ESRRB transcript variant X7	XM_047431080.1:c.412+6629… XM_047431080.1:c.412+6629_412+6631del	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)₁₂=	delTTT	delTT	delT	dupT	dupTT
GRCh38.p14 chr 14	NC_000014.9:g.76446370_76446381=	NC_000014.9:g.76446379_76446381del	NC_000014.9:g.76446380_76446381del	NC_000014.9:g.76446381del	NC_000014.9:g.76446381dup	NC_000014.9:g.76446380_76446381dup
GRCh37.p13 chr 14	NC_000014.8:g.76912713_76912724=	NC_000014.8:g.76912722_76912724del	NC_000014.8:g.76912723_76912724del	NC_000014.8:g.76912724del	NC_000014.8:g.76912724dup	NC_000014.8:g.76912723_76912724dup
ESRRB RefSeqGene	NG_012278.2:g.80024_80035=	NG_012278.2:g.80033_80035del	NG_012278.2:g.80034_80035del	NG_012278.2:g.80035del	NG_012278.2:g.80035dup	NG_012278.2:g.80034_80035dup
ESRRB transcript variant 2	NM_001379180.1:c.460+6620=	NM_001379180.1:c.460+6629_460+6631del	NM_001379180.1:c.460+6630_460+6631del	NM_001379180.1:c.460+6631del	NM_001379180.1:c.460+6631dup	NM_001379180.1:c.460+6630_460+6631dup
ESRRB transcript	NM_004452.3:c.397+6620=	NM_004452.3:c.397+6629_397+6631del	NM_004452.3:c.397+6630_397+6631del	NM_004452.3:c.397+6631del	NM_004452.3:c.397+6631dup	NM_004452.3:c.397+6630_397+6631dup
ESRRB transcript variant 1	NM_004452.4:c.397+6620=	NM_004452.4:c.397+6629_397+6631del	NM_004452.4:c.397+6630_397+6631del	NM_004452.4:c.397+6631del	NM_004452.4:c.397+6631dup	NM_004452.4:c.397+6630_397+6631dup
ESRRB transcript variant X1	XM_005267403.1:c.460+6620=	XM_005267403.1:c.460+6629_460+6631del	XM_005267403.1:c.460+6630_460+6631del	XM_005267403.1:c.460+6631del	XM_005267403.1:c.460+6631dup	XM_005267403.1:c.460+6630_460+6631dup
ESRRB transcript variant X2	XM_005267404.1:c.460+6620=	XM_005267404.1:c.460+6629_460+6631del	XM_005267404.1:c.460+6630_460+6631del	XM_005267404.1:c.460+6631del	XM_005267404.1:c.460+6631dup	XM_005267404.1:c.460+6630_460+6631dup
ESRRB transcript variant X1	XM_011536547.3:c.460+6620=	XM_011536547.3:c.460+6629_460+6631del	XM_011536547.3:c.460+6630_460+6631del	XM_011536547.3:c.460+6631del	XM_011536547.3:c.460+6631dup	XM_011536547.3:c.460+6630_460+6631dup
ESRRB transcript variant X3	XM_011536550.3:c.397+6620=	XM_011536550.3:c.397+6629_397+6631del	XM_011536550.3:c.397+6630_397+6631del	XM_011536550.3:c.397+6631del	XM_011536550.3:c.397+6631dup	XM_011536550.3:c.397+6630_397+6631dup
ESRRB transcript variant X4	XM_011536553.3:c.460+6620=	XM_011536553.3:c.460+6629_460+6631del	XM_011536553.3:c.460+6630_460+6631del	XM_011536553.3:c.460+6631del	XM_011536553.3:c.460+6631dup	XM_011536553.3:c.460+6630_460+6631dup
ESRRB transcript variant X5	XM_011536554.3:c.460+6620=	XM_011536554.3:c.460+6629_460+6631del	XM_011536554.3:c.460+6630_460+6631del	XM_011536554.3:c.460+6631del	XM_011536554.3:c.460+6631dup	XM_011536554.3:c.460+6630_460+6631dup
ESRRB transcript variant X6	XM_024449508.2:c.460+6620=	XM_024449508.2:c.460+6629_460+6631del	XM_024449508.2:c.460+6630_460+6631del	XM_024449508.2:c.460+6631del	XM_024449508.2:c.460+6631dup	XM_024449508.2:c.460+6630_460+6631dup
ESRRB transcript variant X2	XM_047431079.1:c.397+6620=	XM_047431079.1:c.397+6629_397+6631del	XM_047431079.1:c.397+6630_397+6631del	XM_047431079.1:c.397+6631del	XM_047431079.1:c.397+6631dup	XM_047431079.1:c.397+6630_397+6631dup
ESRRB transcript variant X7	XM_047431080.1:c.412+6620=	XM_047431080.1:c.412+6629_412+6631del	XM_047431080.1:c.412+6630_412+6631del	XM_047431080.1:c.412+6631del	XM_047431080.1:c.412+6631dup	XM_047431080.1:c.412+6630_412+6631dup

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#.

59 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss5019473	Aug 28, 2002 (107)
2	ABI	ss40506093	Mar 15, 2016 (147)
3	ABI	ss40507516	Mar 15, 2016 (147)
4	ABI	ss40512628	Mar 15, 2016 (147)
5	HGSV	ss77862468	Aug 21, 2014 (142)
6	HUMANGENOME_JCVI	ss96893366	Dec 05, 2013 (138)
7	BGI	ss104701672	Mar 15, 2016 (147)
8	BUSHMAN	ss193360936	Mar 15, 2016 (147)
9	GMI	ss289231134	May 04, 2012 (138)
10	TISHKOFF	ss554746426	Apr 25, 2013 (138)
11	SSMP	ss664243701	Apr 01, 2015 (144)
12	BILGI_BIOE	ss666632774	Apr 25, 2013 (138)
13	1000GENOMES	ss1374310503	Aug 21, 2014 (142)
14	DDI	ss1536790595	Apr 01, 2015 (144)
15	HAMMER_LAB	ss1807993061	Sep 08, 2015 (146)
16	HAMMER_LAB	ss1807993062	Sep 08, 2015 (146)
17	SYSTEMSBIOZJU	ss2628554427	Nov 08, 2017 (151)
18	SWEGEN	ss3012482808	Nov 08, 2017 (151)
19	BEROUKHIMLAB	ss3644378273	Oct 12, 2018 (152)
20	BIOINF_KMB_FNS_UNIBA	ss3645356794	Oct 12, 2018 (152)
21	URBANLAB	ss3650240777	Oct 12, 2018 (152)
22	EVA_DECODE	ss3697021536	Jul 13, 2019 (153)
23	EVA_DECODE	ss3697021537	Jul 13, 2019 (153)
24	EVA_DECODE	ss3697021538	Jul 13, 2019 (153)
25	EVA_DECODE	ss3697021539	Jul 13, 2019 (153)
26	ACPOP	ss3740534576	Jul 13, 2019 (153)
27	ACPOP	ss3740534577	Jul 13, 2019 (153)
28	PACBIO	ss3787713933	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3817861152	Jul 13, 2019 (153)
30	EVA	ss3834008269	Apr 27, 2020 (154)
31	EVA	ss3840594885	Apr 27, 2020 (154)
32	EVA	ss3846084538	Apr 27, 2020 (154)
33	KOGIC	ss3975278547	Apr 27, 2020 (154)
34	KOGIC	ss3975278548	Apr 27, 2020 (154)
35	KOGIC	ss3975278549	Apr 27, 2020 (154)
36	KOGIC	ss3975278550	Apr 27, 2020 (154)
37	GNOMAD	ss4281027781	Apr 26, 2021 (155)
38	GNOMAD	ss4281027782	Apr 26, 2021 (155)
39	GNOMAD	ss4281027783	Apr 26, 2021 (155)
40	GNOMAD	ss4281027784	Apr 26, 2021 (155)
41	GNOMAD	ss4281027785	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5214012861	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5214012862	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5214012863	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5214012864	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5296827069	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5296827070	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5296827071	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5296827072	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5490812508	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5490812509	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5490812510	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5490812511	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5767044815	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5767044816	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5767044817	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5767044818	Oct 16, 2022 (156)
58	EVA	ss5841348497	Oct 16, 2022 (156)
59	EVA	ss5841348498	Oct 16, 2022 (156)
60	1000Genomes	NC_000014.8 - 76912713	Oct 12, 2018 (152)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456167028 (NC_000014.9:76446369::T 1159/134282) Row 456167029 (NC_000014.9:76446369::TT 1/134370) Row 456167030 (NC_000014.9:76446369:T: 7867/134238)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456167028 (NC_000014.9:76446369::T 1159/134282) Row 456167029 (NC_000014.9:76446369::TT 1/134370) Row 456167030 (NC_000014.9:76446369:T: 7867/134238)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456167028 (NC_000014.9:76446369::T 1159/134282) Row 456167029 (NC_000014.9:76446369::TT 1/134370) Row 456167030 (NC_000014.9:76446369:T: 7867/134238)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456167028 (NC_000014.9:76446369::T 1159/134282) Row 456167029 (NC_000014.9:76446369::TT 1/134370) Row 456167030 (NC_000014.9:76446369:T: 7867/134238)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456167028 (NC_000014.9:76446369::T 1159/134282) Row 456167029 (NC_000014.9:76446369::TT 1/134370) Row 456167030 (NC_000014.9:76446369:T: 7867/134238)...	-	Apr 26, 2021 (155)
66	Korean Genome Project Submission ignored due to conflicting rows: Row 31656548 (NC_000014.9:76446369:TTT: 159/1832) Row 31656549 (NC_000014.9:76446370:TT: 216/1832) Row 31656550 (NC_000014.9:76446371:T: 48/1832)...	-	Apr 27, 2020 (154)
67	Korean Genome Project Submission ignored due to conflicting rows: Row 31656548 (NC_000014.9:76446369:TTT: 159/1832) Row 31656549 (NC_000014.9:76446370:TT: 216/1832) Row 31656550 (NC_000014.9:76446371:T: 48/1832)...	-	Apr 27, 2020 (154)
68	Korean Genome Project Submission ignored due to conflicting rows: Row 31656548 (NC_000014.9:76446369:TTT: 159/1832) Row 31656549 (NC_000014.9:76446370:TT: 216/1832) Row 31656550 (NC_000014.9:76446371:T: 48/1832)...	-	Apr 27, 2020 (154)
69	Korean Genome Project Submission ignored due to conflicting rows: Row 31656548 (NC_000014.9:76446369:TTT: 159/1832) Row 31656549 (NC_000014.9:76446370:TT: 216/1832) Row 31656550 (NC_000014.9:76446371:T: 48/1832)...	-	Apr 27, 2020 (154)
70	Northern Sweden Submission ignored due to conflicting rows: Row 13819441 (NC_000014.8:76912712:TTT: 150/600) Row 13819442 (NC_000014.8:76912712:TT: 17/600)	-	Jul 13, 2019 (153)
71	Northern Sweden Submission ignored due to conflicting rows: Row 13819441 (NC_000014.8:76912712:TTT: 150/600) Row 13819442 (NC_000014.8:76912712:TT: 17/600)	-	Jul 13, 2019 (153)
72	8.3KJPN Submission ignored due to conflicting rows: Row 71982168 (NC_000014.8:76912712:TTT: 1618/16760) Row 71982169 (NC_000014.8:76912712:TT: 1828/16760) Row 71982170 (NC_000014.8:76912712::T 19/16760)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 71982168 (NC_000014.8:76912712:TTT: 1618/16760) Row 71982169 (NC_000014.8:76912712:TT: 1828/16760) Row 71982170 (NC_000014.8:76912712::T 19/16760)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 71982168 (NC_000014.8:76912712:TTT: 1618/16760) Row 71982169 (NC_000014.8:76912712:TT: 1828/16760) Row 71982170 (NC_000014.8:76912712::T 19/16760)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 71982168 (NC_000014.8:76912712:TTT: 1618/16760) Row 71982169 (NC_000014.8:76912712:TT: 1828/16760) Row 71982170 (NC_000014.8:76912712::T 19/16760)...	-	Apr 26, 2021 (155)
76	14KJPN Submission ignored due to conflicting rows: Row 100881919 (NC_000014.9:76446369:TTT: 2781/28258) Row 100881920 (NC_000014.9:76446369:TT: 3064/28258) Row 100881921 (NC_000014.9:76446369:T: 222/28258)...	-	Oct 16, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 100881919 (NC_000014.9:76446369:TTT: 2781/28258) Row 100881920 (NC_000014.9:76446369:TT: 3064/28258) Row 100881921 (NC_000014.9:76446369:T: 222/28258)...	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 100881919 (NC_000014.9:76446369:TTT: 2781/28258) Row 100881920 (NC_000014.9:76446369:TT: 3064/28258) Row 100881921 (NC_000014.9:76446369:T: 222/28258)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 100881919 (NC_000014.9:76446369:TTT: 2781/28258) Row 100881920 (NC_000014.9:76446369:TT: 3064/28258) Row 100881921 (NC_000014.9:76446369:T: 222/28258)...	-	Oct 16, 2022 (156)
80	ALFA	NC_000014.9 - 76446370	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)
rs869028340	Jul 19, 2016 (147)
rs34297199	Jul 30, 2012 (137)
rs34587707	May 11, 2012 (137)
rs67159113	Apr 25, 2013 (138)
rs67159114	Feb 26, 2009 (130)
rs67188979	May 09, 2011 (134)
rs67188980	Feb 26, 2009 (130)
rs72293582	Oct 26, 2010 (133)
rs77393606	May 11, 2012 (137)
rs113400544	Oct 26, 2010 (133)
rs201611632	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss289231134	NC_000014.7:75982465:TTT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTT	(self)
ss77862468	NC_000014.7:75982474:TTT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTT	(self)
64698036, ss664243701, ss666632774, ss1374310503, ss1536790595, ss3012482808, ss3644378273, ss3740534576, ss5214012861, ss5841348497	NC_000014.8:76912712:TTT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTT	(self)
ss3645356794, ss3650240777, ss3697021536, ss3817861152, ss3975278547, ss4281027785, ss5296827069, ss5490812508, ss5767044815	NC_000014.9:76446369:TTT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTT	(self)
3127818790	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTT	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTT	(self)
ss5019473	NT_026437.12:57912712:TTT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTT	(self)
ss96893366	NT_026437.12:57912721:TTT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTT	(self)
ss1807993062, ss3740534577, ss5214012862, ss5841348498	NC_000014.8:76912712:TT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3840594885	NC_000014.8:76912713:TT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss554746426	NC_000014.8:76912722:TT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4281027784, ss5296827072, ss5490812509, ss5767044816	NC_000014.9:76446369:TT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTT	(self)
3127818790	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTT	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3697021537, ss3846084538, ss3975278548	NC_000014.9:76446370:TT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss104701672	NT_026437.12:57912721:TT:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss1807993061, ss2628554427, ss3787713933, ss5214012864	NC_000014.8:76912712:T:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4281027783, ss5296827070, ss5490812510, ss5767044817	NC_000014.9:76446369:T:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
3127818790	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTT	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3697021538, ss3975278549	NC_000014.9:76446371:T:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss40512628, ss193360936	NT_026437.12:57912712:T:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss40507516	NT_026437.12:57912713:T:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss40506093	NT_026437.12:57912714:T:	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3834008269, ss5214012863	NC_000014.8:76912712::T	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4281027781, ss5296827071, ss5490812511, ss5767044818	NC_000014.9:76446369::T	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3127818790	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3697021539, ss3975278550	NC_000014.9:76446372::T	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4281027782	NC_000014.9:76446369::TT	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3127818790	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000014.9:76446369:TTTTTTTTTTTT:… NC_000014.9:76446369:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(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 rs3832965

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

rs3832965