Name: rs113156661
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.

rs113156661

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:73927090-73927103 (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)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.2370 (1727/7286, ALFA)
delT=0.3826 (544/1422, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FAM161B : Intron Variant
ZNF410 : 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	7286	TTTTTTTTTTTTTT=0.6803	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0332, TTTTTTTTTTTTTTT=0.2370, TTTTTTTTTTTTTTTT=0.0457, TTTTTTTTTTTTTTTTT=0.0037	0.640554	0.127015	0.232431	32
European	Sub	6188	TTTTTTTTTTTTTT=0.6238	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0391, TTTTTTTTTTTTTTT=0.2791, TTTTTTTTTTTTTTTT=0.0537, TTTTTTTTTTTTTTTTT=0.0044	0.56343	0.154268	0.282302	32
African	Sub	722	TTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	34	TTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	688	TTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	40	TTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	32	TTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	34	TTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	182	TTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	8	TTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	112	TTTTTTTTTTTTTT=0.991	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.009, TTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	7286	(T)₁₄=0.6803	del(T)₄=0.0000, delTT=0.0000, delT=0.0332, dupT=0.2370, dupTT=0.0457, dupTTT=0.0037
Allele Frequency Aggregator	European	Sub	6188	(T)₁₄=0.6238	del(T)₄=0.0000, delTT=0.0000, delT=0.0391, dupT=0.2791, dupTT=0.0537, dupTTT=0.0044
Allele Frequency Aggregator	African	Sub	722	(T)₁₄=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 2	Sub	182	(T)₁₄=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	Other	Sub	112	(T)₁₄=0.991	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.009, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	40	(T)₁₄=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	Latin American 1	Sub	34	(T)₁₄=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	8	(T)₁₄=1.0	del(T)₄=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0
1000Genomes	Global	Study-wide	1422	(T)₁₄=0.6174	delT=0.3826
1000Genomes	East Asian	Sub	454	(T)₁₄=0.879	delT=0.121
1000Genomes	South Asian	Sub	408	(T)₁₄=0.694	delT=0.306
1000Genomes	African	Sub	315	(T)₁₄=0.117	delT=0.883
1000Genomes	Europe	Sub	125	(T)₁₄=0.712	delT=0.288
1000Genomes	American	Sub	120	(T)₁₄=0.583	delT=0.417

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.73927100_73927103del
GRCh38.p14 chr 14	NC_000014.9:g.73927101_73927103del
GRCh38.p14 chr 14	NC_000014.9:g.73927102_73927103del
GRCh38.p14 chr 14	NC_000014.9:g.73927103del
GRCh38.p14 chr 14	NC_000014.9:g.73927103dup
GRCh38.p14 chr 14	NC_000014.9:g.73927102_73927103dup
GRCh38.p14 chr 14	NC_000014.9:g.73927101_73927103dup
GRCh38.p14 chr 14	NC_000014.9:g.73927093_73927103dup
GRCh37.p13 chr 14	NC_000014.8:g.74393803_74393806del
GRCh37.p13 chr 14	NC_000014.8:g.74393804_74393806del
GRCh37.p13 chr 14	NC_000014.8:g.74393805_74393806del
GRCh37.p13 chr 14	NC_000014.8:g.74393806del
GRCh37.p13 chr 14	NC_000014.8:g.74393806dup
GRCh37.p13 chr 14	NC_000014.8:g.74393805_74393806dup
GRCh37.p13 chr 14	NC_000014.8:g.74393804_74393806dup
GRCh37.p13 chr 14	NC_000014.8:g.74393796_74393806dup

Gene: ZNF410, zinc finger protein 410 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF410 transcript variant 1	NM_001242924.2:c.16+2281… NM_001242924.2:c.16+2281_*16+2284del	N/A	Intron Variant
ZNF410 transcript variant 3	NM_001242926.2:c.1257+357… NM_001242926.2:c.1257+3578_1257+3581del	N/A	Intron Variant
ZNF410 transcript variant 4	NM_001242927.2:c.1179+357… NM_001242927.2:c.1179+3578_1179+3581del	N/A	Intron Variant
ZNF410 transcript variant 5	NM_001242928.2:c.811-7_81… NM_001242928.2:c.811-7_811-4del	N/A	Intron Variant
ZNF410 transcript variant 2	NM_021188.3:c.1398+3578_1… NM_021188.3:c.1398+3578_1398+3581del	N/A	Intron Variant
ZNF410 transcript variant 6	NR_040251.2:n.	N/A	Intron Variant

Gene: FAM161B, FAM161 centrosomal protein B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FAM161B transcript	NM_152445.3:c.	N/A	Genic Downstream Transcript Variant
FAM161B transcript variant X1	XM_011536475.3:c.	N/A	Genic Downstream Transcript Variant
FAM161B transcript variant X2	XR_007063990.1:n.	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)₁₄=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₁₁
GRCh38.p14 chr 14	NC_000014.9:g.73927090_73927103=	NC_000014.9:g.73927100_73927103del	NC_000014.9:g.73927101_73927103del	NC_000014.9:g.73927102_73927103del	NC_000014.9:g.73927103del	NC_000014.9:g.73927103dup	NC_000014.9:g.73927102_73927103dup	NC_000014.9:g.73927101_73927103dup	NC_000014.9:g.73927093_73927103dup
GRCh37.p13 chr 14	NC_000014.8:g.74393793_74393806=	NC_000014.8:g.74393803_74393806del	NC_000014.8:g.74393804_74393806del	NC_000014.8:g.74393805_74393806del	NC_000014.8:g.74393806del	NC_000014.8:g.74393806dup	NC_000014.8:g.74393805_74393806dup	NC_000014.8:g.74393804_74393806dup	NC_000014.8:g.74393796_74393806dup
ZNF410 transcript variant 1	NM_001242924.1:c.*16+2271=	NM_001242924.1:c.16+2281_16+2284del	NM_001242924.1:c.16+2282_16+2284del	NM_001242924.1:c.16+2283_16+2284del	NM_001242924.1:c.*16+2284del	NM_001242924.1:c.*16+2284dup	NM_001242924.1:c.16+2283_16+2284dup	NM_001242924.1:c.16+2282_16+2284dup	NM_001242924.1:c.16+2274_16+2284dup
ZNF410 transcript variant 1	NM_001242924.2:c.*16+2271=	NM_001242924.2:c.16+2281_16+2284del	NM_001242924.2:c.16+2282_16+2284del	NM_001242924.2:c.16+2283_16+2284del	NM_001242924.2:c.*16+2284del	NM_001242924.2:c.*16+2284dup	NM_001242924.2:c.16+2283_16+2284dup	NM_001242924.2:c.16+2282_16+2284dup	NM_001242924.2:c.16+2274_16+2284dup
ZNF410 transcript variant 3	NM_001242926.1:c.1257+3568=	NM_001242926.1:c.1257+3578_1257+3581del	NM_001242926.1:c.1257+3579_1257+3581del	NM_001242926.1:c.1257+3580_1257+3581del	NM_001242926.1:c.1257+3581del	NM_001242926.1:c.1257+3581dup	NM_001242926.1:c.1257+3580_1257+3581dup	NM_001242926.1:c.1257+3579_1257+3581dup	NM_001242926.1:c.1257+3571_1257+3581dup
ZNF410 transcript variant 3	NM_001242926.2:c.1257+3568=	NM_001242926.2:c.1257+3578_1257+3581del	NM_001242926.2:c.1257+3579_1257+3581del	NM_001242926.2:c.1257+3580_1257+3581del	NM_001242926.2:c.1257+3581del	NM_001242926.2:c.1257+3581dup	NM_001242926.2:c.1257+3580_1257+3581dup	NM_001242926.2:c.1257+3579_1257+3581dup	NM_001242926.2:c.1257+3571_1257+3581dup
ZNF410 transcript variant 4	NM_001242927.1:c.1179+3568=	NM_001242927.1:c.1179+3578_1179+3581del	NM_001242927.1:c.1179+3579_1179+3581del	NM_001242927.1:c.1179+3580_1179+3581del	NM_001242927.1:c.1179+3581del	NM_001242927.1:c.1179+3581dup	NM_001242927.1:c.1179+3580_1179+3581dup	NM_001242927.1:c.1179+3579_1179+3581dup	NM_001242927.1:c.1179+3571_1179+3581dup
ZNF410 transcript variant 4	NM_001242927.2:c.1179+3568=	NM_001242927.2:c.1179+3578_1179+3581del	NM_001242927.2:c.1179+3579_1179+3581del	NM_001242927.2:c.1179+3580_1179+3581del	NM_001242927.2:c.1179+3581del	NM_001242927.2:c.1179+3581dup	NM_001242927.2:c.1179+3580_1179+3581dup	NM_001242927.2:c.1179+3579_1179+3581dup	NM_001242927.2:c.1179+3571_1179+3581dup
ZNF410 transcript variant 5	NM_001242928.1:c.811-17=	NM_001242928.1:c.811-7_811-4del	NM_001242928.1:c.811-6_811-4del	NM_001242928.1:c.811-5_811-4del	NM_001242928.1:c.811-4del	NM_001242928.1:c.811-4dup	NM_001242928.1:c.811-5_811-4dup	NM_001242928.1:c.811-6_811-4dup	NM_001242928.1:c.811-14_811-4dup
ZNF410 transcript variant 5	NM_001242928.2:c.811-17=	NM_001242928.2:c.811-7_811-4del	NM_001242928.2:c.811-6_811-4del	NM_001242928.2:c.811-5_811-4del	NM_001242928.2:c.811-4del	NM_001242928.2:c.811-4dup	NM_001242928.2:c.811-5_811-4dup	NM_001242928.2:c.811-6_811-4dup	NM_001242928.2:c.811-14_811-4dup
ZNF410 transcript variant 2	NM_021188.2:c.1398+3568=	NM_021188.2:c.1398+3578_1398+3581del	NM_021188.2:c.1398+3579_1398+3581del	NM_021188.2:c.1398+3580_1398+3581del	NM_021188.2:c.1398+3581del	NM_021188.2:c.1398+3581dup	NM_021188.2:c.1398+3580_1398+3581dup	NM_021188.2:c.1398+3579_1398+3581dup	NM_021188.2:c.1398+3571_1398+3581dup
ZNF410 transcript variant 2	NM_021188.3:c.1398+3568=	NM_021188.3:c.1398+3578_1398+3581del	NM_021188.3:c.1398+3579_1398+3581del	NM_021188.3:c.1398+3580_1398+3581del	NM_021188.3:c.1398+3581del	NM_021188.3:c.1398+3581dup	NM_021188.3:c.1398+3580_1398+3581dup	NM_021188.3:c.1398+3579_1398+3581dup	NM_021188.3:c.1398+3571_1398+3581dup

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#.

66 SubSNP, 38 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80001160	Dec 04, 2013 (138)
2	BGI	ss104701571	Dec 06, 2013 (138)
3	BUSHMAN	ss193359942	Jul 04, 2010 (132)
4	GMI	ss289230183	Oct 12, 2018 (152)
5	SSMP	ss664242429	Apr 01, 2015 (144)
6	BILGI_BIOE	ss666632129	Apr 25, 2013 (138)
7	1000GENOMES	ss1374285818	Aug 21, 2014 (142)
8	1000GENOMES	ss1374285819	Oct 12, 2018 (152)
9	1000GENOMES	ss1374285820	Oct 12, 2018 (152)
10	DDI	ss1536790041	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1708119079	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1708119081	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1708119333	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1708119334	Apr 01, 2015 (144)
15	EVA_EXAC	ss1712059315	Apr 01, 2015 (144)
16	EVA_EXAC	ss1712059316	Apr 01, 2015 (144)
17	EVA_EXAC	ss1712059317	Apr 01, 2015 (144)
18	EVA_EXAC	ss1712059318	Apr 01, 2015 (144)
19	EVA_EXAC	ss1712059319	Jan 10, 2018 (151)
20	SYSTEMSBIOZJU	ss2628549937	Nov 08, 2017 (151)
21	SWEGEN	ss3012455035	Nov 08, 2017 (151)
22	EVA_DECODE	ss3696986313	Jul 13, 2019 (153)
23	EVA_DECODE	ss3696986314	Jul 13, 2019 (153)
24	EVA_DECODE	ss3696986315	Jul 13, 2019 (153)
25	EVA_DECODE	ss3696986316	Jul 13, 2019 (153)
26	EVA_DECODE	ss3696986317	Jul 13, 2019 (153)
27	ACPOP	ss3740519591	Jul 13, 2019 (153)
28	ACPOP	ss3740519592	Jul 13, 2019 (153)
29	ACPOP	ss3740519593	Jul 13, 2019 (153)
30	ACPOP	ss3740519594	Jul 13, 2019 (153)
31	PACBIO	ss3787708662	Jul 13, 2019 (153)
32	PACBIO	ss3792739880	Jul 13, 2019 (153)
33	PACBIO	ss3797624249	Jul 13, 2019 (153)
34	KHV_HUMAN_GENOMES	ss3817840752	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3817840753	Jul 13, 2019 (153)
36	KHV_HUMAN_GENOMES	ss3817840754	Jul 13, 2019 (153)
37	EVA	ss3833999567	Apr 27, 2020 (154)
38	KOGIC	ss3975240159	Apr 27, 2020 (154)
39	KOGIC	ss3975240160	Apr 27, 2020 (154)
40	KOGIC	ss3975240161	Apr 27, 2020 (154)
41	KOGIC	ss3975240162	Apr 27, 2020 (154)
42	GNOMAD	ss4280728674	Apr 27, 2021 (155)
43	GNOMAD	ss4280728675	Apr 27, 2021 (155)
44	GNOMAD	ss4280728676	Apr 27, 2021 (155)
45	GNOMAD	ss4280728678	Apr 27, 2021 (155)
46	GNOMAD	ss4280728679	Apr 27, 2021 (155)
47	TOMMO_GENOMICS	ss5213933870	Apr 27, 2021 (155)
48	TOMMO_GENOMICS	ss5213933871	Apr 27, 2021 (155)
49	TOMMO_GENOMICS	ss5213933872	Apr 27, 2021 (155)
50	TOMMO_GENOMICS	ss5213933873	Apr 27, 2021 (155)
51	EVA	ss5237227015	Apr 27, 2021 (155)
52	1000G_HIGH_COVERAGE	ss5296766355	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5296766356	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5296766357	Oct 16, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5296766358	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5490757356	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5490757357	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5490757358	Oct 16, 2022 (156)
59	HUGCELL_USP	ss5490757359	Oct 16, 2022 (156)
60	EVA	ss5624046750	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5766941535	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5766941536	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5766941537	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5766941538	Oct 16, 2022 (156)
65	EVA	ss5841324554	Oct 16, 2022 (156)
66	EVA	ss5841324555	Oct 16, 2022 (156)
67	1000Genomes	NC_000014.8 - 74393793	Oct 12, 2018 (152)
68	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 35912297 (NC_000014.8:74393792::T 1448/3854) Row 35912298 (NC_000014.8:74393792::TT 443/3854)	-	Oct 12, 2018 (152)
69	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 35912297 (NC_000014.8:74393792::T 1448/3854) Row 35912298 (NC_000014.8:74393792::TT 443/3854)	-	Oct 12, 2018 (152)
70	ExAC Submission ignored due to conflicting rows: Row 1903686 (NC_000014.8:74393792:TT: 0/6) Row 1903687 (NC_000014.8:74393792:T: 2/6) Row 1903688 (NC_000014.8:74393792::T 0/6) Row 1903689 (NC_000014.8:74393792::TT 1/6) Row 1903690 (NC_000014.8:74393792::TTT 0/6)	-	Oct 12, 2018 (152)
71	ExAC Submission ignored due to conflicting rows: Row 1903686 (NC_000014.8:74393792:TT: 0/6) Row 1903687 (NC_000014.8:74393792:T: 2/6) Row 1903688 (NC_000014.8:74393792::T 0/6) Row 1903689 (NC_000014.8:74393792::TT 1/6) Row 1903690 (NC_000014.8:74393792::TTT 0/6)	-	Oct 12, 2018 (152)
72	ExAC Submission ignored due to conflicting rows: Row 1903686 (NC_000014.8:74393792:TT: 0/6) Row 1903687 (NC_000014.8:74393792:T: 2/6) Row 1903688 (NC_000014.8:74393792::T 0/6) Row 1903689 (NC_000014.8:74393792::TT 1/6) Row 1903690 (NC_000014.8:74393792::TTT 0/6)	-	Oct 12, 2018 (152)
73	ExAC Submission ignored due to conflicting rows: Row 1903686 (NC_000014.8:74393792:TT: 0/6) Row 1903687 (NC_000014.8:74393792:T: 2/6) Row 1903688 (NC_000014.8:74393792::T 0/6) Row 1903689 (NC_000014.8:74393792::TT 1/6) Row 1903690 (NC_000014.8:74393792::TTT 0/6)	-	Oct 12, 2018 (152)
74	ExAC Submission ignored due to conflicting rows: Row 1903686 (NC_000014.8:74393792:TT: 0/6) Row 1903687 (NC_000014.8:74393792:T: 2/6) Row 1903688 (NC_000014.8:74393792::T 0/6) Row 1903689 (NC_000014.8:74393792::TT 1/6) Row 1903690 (NC_000014.8:74393792::TTT 0/6)	-	Oct 12, 2018 (152)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455667454 (NC_000014.9:73927089::T 45239/134282) Row 455667455 (NC_000014.9:73927089::TT 13036/134314) Row 455667456 (NC_000014.9:73927089::TTT 193/134410)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455667454 (NC_000014.9:73927089::T 45239/134282) Row 455667455 (NC_000014.9:73927089::TT 13036/134314) Row 455667456 (NC_000014.9:73927089::TTT 193/134410)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455667454 (NC_000014.9:73927089::T 45239/134282) Row 455667455 (NC_000014.9:73927089::TT 13036/134314) Row 455667456 (NC_000014.9:73927089::TTT 193/134410)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455667454 (NC_000014.9:73927089::T 45239/134282) Row 455667455 (NC_000014.9:73927089::TT 13036/134314) Row 455667456 (NC_000014.9:73927089::TTT 193/134410)...	-	Apr 27, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455667454 (NC_000014.9:73927089::T 45239/134282) Row 455667455 (NC_000014.9:73927089::TT 13036/134314) Row 455667456 (NC_000014.9:73927089::TTT 193/134410)...	-	Apr 27, 2021 (155)
80	gnomAD - Exomes Submission ignored due to conflicting rows: Row 10080954 (NC_000014.8:74393792::T 129/448) Row 10080955 (NC_000014.8:74393792::TT 53/448) Row 10080956 (NC_000014.8:74393792::TTT 1/448)...	-	Jul 13, 2019 (153)
81	gnomAD - Exomes Submission ignored due to conflicting rows: Row 10080954 (NC_000014.8:74393792::T 129/448) Row 10080955 (NC_000014.8:74393792::TT 53/448) Row 10080956 (NC_000014.8:74393792::TTT 1/448)...	-	Jul 13, 2019 (153)
82	gnomAD - Exomes Submission ignored due to conflicting rows: Row 10080954 (NC_000014.8:74393792::T 129/448) Row 10080955 (NC_000014.8:74393792::TT 53/448) Row 10080956 (NC_000014.8:74393792::TTT 1/448)...	-	Jul 13, 2019 (153)
83	gnomAD - Exomes Submission ignored due to conflicting rows: Row 10080954 (NC_000014.8:74393792::T 129/448) Row 10080955 (NC_000014.8:74393792::TT 53/448) Row 10080956 (NC_000014.8:74393792::TTT 1/448)...	-	Jul 13, 2019 (153)
84	gnomAD - Exomes Submission ignored due to conflicting rows: Row 10080954 (NC_000014.8:74393792::T 129/448) Row 10080955 (NC_000014.8:74393792::TT 53/448) Row 10080956 (NC_000014.8:74393792::TTT 1/448)...	-	Jul 13, 2019 (153)
85	gnomAD - Exomes Submission ignored due to conflicting rows: Row 10080954 (NC_000014.8:74393792::T 129/448) Row 10080955 (NC_000014.8:74393792::TT 53/448) Row 10080956 (NC_000014.8:74393792::TTT 1/448)...	-	Jul 13, 2019 (153)
86	Korean Genome Project Submission ignored due to conflicting rows: Row 31618160 (NC_000014.9:73927090::T 167/1832) Row 31618161 (NC_000014.9:73927090::TT 765/1832) Row 31618162 (NC_000014.9:73927089:T: 142/1832)...	-	Apr 27, 2020 (154)
87	Korean Genome Project Submission ignored due to conflicting rows: Row 31618160 (NC_000014.9:73927090::T 167/1832) Row 31618161 (NC_000014.9:73927090::TT 765/1832) Row 31618162 (NC_000014.9:73927089:T: 142/1832)...	-	Apr 27, 2020 (154)
88	Korean Genome Project Submission ignored due to conflicting rows: Row 31618160 (NC_000014.9:73927090::T 167/1832) Row 31618161 (NC_000014.9:73927090::TT 765/1832) Row 31618162 (NC_000014.9:73927089:T: 142/1832)...	-	Apr 27, 2020 (154)
89	Korean Genome Project Submission ignored due to conflicting rows: Row 31618160 (NC_000014.9:73927090::T 167/1832) Row 31618161 (NC_000014.9:73927090::TT 765/1832) Row 31618162 (NC_000014.9:73927089:T: 142/1832)...	-	Apr 27, 2020 (154)
90	Northern Sweden Submission ignored due to conflicting rows: Row 13804456 (NC_000014.8:74393792::T 170/596) Row 13804457 (NC_000014.8:74393792::TT 56/596) Row 13804458 (NC_000014.8:74393792::TTT 6/596)...	-	Jul 13, 2019 (153)
91	Northern Sweden Submission ignored due to conflicting rows: Row 13804456 (NC_000014.8:74393792::T 170/596) Row 13804457 (NC_000014.8:74393792::TT 56/596) Row 13804458 (NC_000014.8:74393792::TTT 6/596)...	-	Jul 13, 2019 (153)
92	Northern Sweden Submission ignored due to conflicting rows: Row 13804456 (NC_000014.8:74393792::T 170/596) Row 13804457 (NC_000014.8:74393792::TT 56/596) Row 13804458 (NC_000014.8:74393792::TTT 6/596)...	-	Jul 13, 2019 (153)
93	Northern Sweden Submission ignored due to conflicting rows: Row 13804456 (NC_000014.8:74393792::T 170/596) Row 13804457 (NC_000014.8:74393792::TT 56/596) Row 13804458 (NC_000014.8:74393792::TTT 6/596)...	-	Jul 13, 2019 (153)
94	8.3KJPN Submission ignored due to conflicting rows: Row 71903177 (NC_000014.8:74393792::TT 6738/16754) Row 71903178 (NC_000014.8:74393792::T 1485/16754) Row 71903179 (NC_000014.8:74393792:T: 1450/16754)...	-	Apr 27, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 71903177 (NC_000014.8:74393792::TT 6738/16754) Row 71903178 (NC_000014.8:74393792::T 1485/16754) Row 71903179 (NC_000014.8:74393792:T: 1450/16754)...	-	Apr 27, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 71903177 (NC_000014.8:74393792::TT 6738/16754) Row 71903178 (NC_000014.8:74393792::T 1485/16754) Row 71903179 (NC_000014.8:74393792:T: 1450/16754)...	-	Apr 27, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 71903177 (NC_000014.8:74393792::TT 6738/16754) Row 71903178 (NC_000014.8:74393792::T 1485/16754) Row 71903179 (NC_000014.8:74393792:T: 1450/16754)...	-	Apr 27, 2021 (155)
98	14KJPN Submission ignored due to conflicting rows: Row 100778639 (NC_000014.9:73927089::TT 11327/28258) Row 100778640 (NC_000014.9:73927089::T 2463/28258) Row 100778641 (NC_000014.9:73927089:T: 2485/28258)...	-	Oct 16, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 100778639 (NC_000014.9:73927089::TT 11327/28258) Row 100778640 (NC_000014.9:73927089::T 2463/28258) Row 100778641 (NC_000014.9:73927089:T: 2485/28258)...	-	Oct 16, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 100778639 (NC_000014.9:73927089::TT 11327/28258) Row 100778640 (NC_000014.9:73927089::T 2463/28258) Row 100778641 (NC_000014.9:73927089:T: 2485/28258)...	-	Oct 16, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 100778639 (NC_000014.9:73927089::TT 11327/28258) Row 100778640 (NC_000014.9:73927089::T 2463/28258) Row 100778641 (NC_000014.9:73927089:T: 2485/28258)...	-	Oct 16, 2022 (156)
102	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35912297 (NC_000014.8:74393792::T 1369/3708) Row 35912298 (NC_000014.8:74393792::TT 431/3708)	-	Oct 12, 2018 (152)
103	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35912297 (NC_000014.8:74393792::T 1369/3708) Row 35912298 (NC_000014.8:74393792::TT 431/3708)	-	Oct 12, 2018 (152)
104	ALFA	NC_000014.9 - 73927090	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)
rs369140150	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
3491352513	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
	NC_000014.8:74393792:TTT:	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss1712059319	NC_000014.8:74393792:TT:	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4280728679	NC_000014.9:73927089:TT:	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
3491352513	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
64626433, ss666632129, ss1374285818, ss1712059315, ss3012455035, ss3740519594, ss5213933872	NC_000014.8:74393792:T:	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3696986313, ss3817840753, ss3975240161, ss4280728678, ss5296766355, ss5490757356, ss5766941537	NC_000014.9:73927089:T:	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3491352513	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss193359942	NT_026437.13:55703566:T:	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss1708119079, ss1708119333, ss1712059316, ss3740519591, ss3787708662, ss3792739880, ss3797624249, ss3833999567, ss5213933871, ss5624046750, ss5841324554	NC_000014.8:74393792::T	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss1374285819	NC_000014.8:74393793::T	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4280728674, ss5237227015, ss5296766357, ss5490757357, ss5766941536	NC_000014.9:73927089::T	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3491352513	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3696986314, ss3817840754, ss3975240159	NC_000014.9:73927090::T	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss80001160	NT_026437.12:55393806::T	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss289230183	NC_000014.7:73463559::TT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss664242429, ss1536790041, ss1708119081, ss1708119334, ss1712059317, ss2628549937, ss3740519592, ss5213933870, ss5841324555	NC_000014.8:74393792::TT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss1374285820	NC_000014.8:74393793::TT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4280728675, ss5296766356, ss5490757358, ss5766941535	NC_000014.9:73927089::TT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
3491352513	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3696986315, ss3817840752, ss3975240160	NC_000014.9:73927090::TT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss104701571	NT_026437.12:55393805::TT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss1712059318, ss3740519593, ss5213933873	NC_000014.8:74393792::TTT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4280728676, ss5296766358, ss5490757359, ss5766941538	NC_000014.9:73927089::TTT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3491352513	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3696986316, ss3975240162	NC_000014.9:73927090::TTT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3696986317	NC_000014.9:73927090::TTTTTTTTTTT	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3215238714	NC_000014.9:73927089:TTTT:	NC_000014.9:73927089:TTTTTTTTTTTTT… NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs113156661

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

rs113156661