Name: rs149255221
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.

rs149255221

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:51365392-51365401 (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 / delT / dupT / d…
del(T)₄ / delTTT / delT / dupT / dupTT / ins(T)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1073 (1017/9476, ALFA)
delT=0.2223 (948/4265, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: INTS6 : 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	9476	TTTTTTTTTT=0.7999	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTTT=0.0928, TTTTTTTTTTT=0.1073, TTTTTTTTTTTT=0.0000	0.819332	0.030111	0.150557	32
European	Sub	7144	TTTTTTTTTT=0.7350	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTTT=0.1229, TTTTTTTTTTT=0.1421, TTTTTTTTTTTT=0.0000	0.744528	0.042698	0.212774	32
African	Sub	1784	TTTTTTTTTT=1.0000	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	70	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1714	TTTTTTTTTT=1.0000	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	50	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	40	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	TTTTTTTTTT=1.0	TTTTTT=0.0, TTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	62	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	180	TTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	24	TTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	232	TTTTTTTTTT=0.987	TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTTT=0.004, TTTTTTTTTTT=0.009, TTTTTTTTTTTT=0.000	0.982609	0.0	0.017391	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9476	(T)₁₀=0.7999	del(T)₄=0.0000, delTTT=0.0000, delT=0.0928, dupT=0.1073, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	7144	(T)₁₀=0.7350	del(T)₄=0.0000, delTTT=0.0000, delT=0.1229, dupT=0.1421, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	1784	(T)₁₀=1.0000	del(T)₄=0.0000, delTTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Other	Sub	232	(T)₁₀=0.987	del(T)₄=0.000, delTTT=0.000, delT=0.004, dupT=0.009, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	180	(T)₁₀=1.000	del(T)₄=0.000, delTTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	62	(T)₁₀=1.00	del(T)₄=0.00, delTTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	50	(T)₁₀=1.00	del(T)₄=0.00, delTTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(T)₁₀=1.00	del(T)₄=0.00, delTTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	4265	(T)₁₀=0.7777	delT=0.2223
1000Genomes	African	Sub	1295	(T)₁₀=0.8409	delT=0.1591
1000Genomes	East Asian	Sub	898	(T)₁₀=0.732	delT=0.268
1000Genomes	Europe	Sub	776	(T)₁₀=0.756	delT=0.244
1000Genomes	South Asian	Sub	695	(T)₁₀=0.824	delT=0.176
1000Genomes	American	Sub	601	(T)₁₀=0.684	delT=0.316

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 13	NC_000013.11:g.51365398_51365401del
GRCh38.p14 chr 13	NC_000013.11:g.51365399_51365401del
GRCh38.p14 chr 13	NC_000013.11:g.51365401del
GRCh38.p14 chr 13	NC_000013.11:g.51365401dup
GRCh38.p14 chr 13	NC_000013.11:g.51365400_51365401dup
GRCh38.p14 chr 13	NC_000013.11:g.51365401_51365402insTTTTTTTTTTT
GRCh37.p13 chr 13	NC_000013.10:g.51939534_51939537del
GRCh37.p13 chr 13	NC_000013.10:g.51939535_51939537del
GRCh37.p13 chr 13	NC_000013.10:g.51939537del
GRCh37.p13 chr 13	NC_000013.10:g.51939537dup
GRCh37.p13 chr 13	NC_000013.10:g.51939536_51939537dup
GRCh37.p13 chr 13	NC_000013.10:g.51939537_51939538insTTTTTTTTTTT

Gene: INTS6, integrator complex subunit 6 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
INTS6 transcript variant 1	NM_012141.3:c.351_360=	N/A	3 Prime UTR Variant
INTS6 transcript variant 4	NM_001306091.2:c.351_36… NM_001306091.2:c.351_360=	N/A	3 Prime UTR Variant
INTS6 transcript variant 2	NM_001039937.2:c.351_36… NM_001039937.2:c.351_360=	N/A	3 Prime UTR Variant
INTS6 transcript variant 3	NM_001039938.2:c.	N/A	Genic Downstream Transcript Variant
INTS6 transcript variant X1	XM_011535040.4:c.49+308_… XM_011535040.4:c.49+308_*49+311del	N/A	Intron Variant
INTS6 transcript variant X6	XM_047430264.1:c.351_36… XM_047430264.1:c.351_360=	N/A	3 Prime UTR Variant
INTS6 transcript variant X7	XM_047430265.1:c.351_36… XM_047430265.1:c.351_360=	N/A	3 Prime UTR Variant
INTS6 transcript variant X2	XR_007063673.1:n.	N/A	Intron Variant
INTS6 transcript variant X3	XR_007063674.1:n.	N/A	Intron Variant
INTS6 transcript variant X4	XR_007063675.1:n.	N/A	Intron Variant
INTS6 transcript variant X5	XR_007063676.1: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)₁₀=	del(T)₄	delTTT	delT	dupT	dupTT	ins(T)₁₁
GRCh38.p14 chr 13	NC_000013.11:g.51365392_51365401=	NC_000013.11:g.51365398_51365401del	NC_000013.11:g.51365399_51365401del	NC_000013.11:g.51365401del	NC_000013.11:g.51365401dup	NC_000013.11:g.51365400_51365401dup	NC_000013.11:g.51365401_51365402insTTTTTTTTTTT
GRCh37.p13 chr 13	NC_000013.10:g.51939528_51939537=	NC_000013.10:g.51939534_51939537del	NC_000013.10:g.51939535_51939537del	NC_000013.10:g.51939537del	NC_000013.10:g.51939537dup	NC_000013.10:g.51939536_51939537dup	NC_000013.10:g.51939537_51939538insTTTTTTTTTTT
INTS6 transcript variant 1	NM_012141.3:c.351_360=	NM_012141.3:c.357_360del	NM_012141.3:c.358_360del	NM_012141.3:c.*360del	NM_012141.3:c.*360dup	NM_012141.3:c.359_360dup	NM_012141.3:c.360_361insAAAAAAAAAAA
INTS6 transcript variant 1	NM_012141.2:c.351_360=	NM_012141.2:c.357_360del	NM_012141.2:c.358_360del	NM_012141.2:c.*360del	NM_012141.2:c.*360dup	NM_012141.2:c.359_360dup	NM_012141.2:c.360_361insAAAAAAAAAAA
INTS6 transcript variant 4	NM_001306091.2:c.351_360=	NM_001306091.2:c.357_360del	NM_001306091.2:c.358_360del	NM_001306091.2:c.*360del	NM_001306091.2:c.*360dup	NM_001306091.2:c.359_360dup	NM_001306091.2:c.360_361insAAAAAAAAAAA
INTS6 transcript variant 4	NM_001306091.1:c.351_360=	NM_001306091.1:c.357_360del	NM_001306091.1:c.358_360del	NM_001306091.1:c.*360del	NM_001306091.1:c.*360dup	NM_001306091.1:c.359_360dup	NM_001306091.1:c.360_361insAAAAAAAAAAA
INTS6 transcript variant 2	NM_001039937.2:c.351_360=	NM_001039937.2:c.357_360del	NM_001039937.2:c.358_360del	NM_001039937.2:c.*360del	NM_001039937.2:c.*360dup	NM_001039937.2:c.359_360dup	NM_001039937.2:c.360_361insAAAAAAAAAAA
INTS6 transcript variant 2	NM_001039937.1:c.351_360=	NM_001039937.1:c.357_360del	NM_001039937.1:c.358_360del	NM_001039937.1:c.*360del	NM_001039937.1:c.*360dup	NM_001039937.1:c.359_360dup	NM_001039937.1:c.360_361insAAAAAAAAAAA
INTS6 transcript variant X6	XM_047430264.1:c.351_360=	XM_047430264.1:c.357_360del	XM_047430264.1:c.358_360del	XM_047430264.1:c.*360del	XM_047430264.1:c.*360dup	XM_047430264.1:c.359_360dup	XM_047430264.1:c.360_361insAAAAAAAAAAA
INTS6 transcript variant X7	XM_047430265.1:c.351_360=	XM_047430265.1:c.357_360del	XM_047430265.1:c.358_360del	XM_047430265.1:c.*360del	XM_047430265.1:c.*360dup	XM_047430265.1:c.359_360dup	XM_047430265.1:c.360_361insAAAAAAAAAAA
INTS6 transcript variant X1	XM_005266339.1:c.*49+311=	XM_005266339.1:c.49+308_49+311del	XM_005266339.1:c.49+309_49+311del	XM_005266339.1:c.*49+311del	XM_005266339.1:c.*49+311dup	XM_005266339.1:c.49+310_49+311dup	XM_005266339.1:c.49+311_49+312insAAAAAAAAAAA
INTS6 transcript variant X1	XM_011535040.4:c.*49+311=	XM_011535040.4:c.49+308_49+311del	XM_011535040.4:c.49+309_49+311del	XM_011535040.4:c.*49+311del	XM_011535040.4:c.*49+311dup	XM_011535040.4:c.49+310_49+311dup	XM_011535040.4:c.49+311_49+312insAAAAAAAAAAA

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#.

56 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss289177914	May 04, 2012 (137)
2	GMI	ss289177915	May 04, 2012 (137)
3	1000GENOMES	ss327526909	May 09, 2011 (134)
4	1000GENOMES	ss327628673	Jan 10, 2018 (151)
5	1000GENOMES	ss328074474	May 09, 2011 (134)
6	LUNTER	ss552293017	Apr 25, 2013 (138)
7	LUNTER	ss552600198	Apr 25, 2013 (138)
8	LUNTER	ss553519555	Apr 25, 2013 (138)
9	SSMP	ss664181422	Apr 01, 2015 (144)
10	BILGI_BIOE	ss666599371	Apr 25, 2013 (138)
11	1000GENOMES	ss1373167708	Aug 21, 2014 (142)
12	1000GENOMES	ss1373167711	Aug 21, 2014 (142)
13	EVA_UK10K_ALSPAC	ss1707788876	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1707789015	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1710602394	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1710602401	Apr 01, 2015 (144)
17	TMC_SNPDB	ss1997060616	Jul 19, 2016 (147)
18	SYSTEMSBIOZJU	ss2628312375	Jan 10, 2018 (151)
19	MCHAISSO	ss3064596482	Nov 08, 2017 (151)
20	BIOINF_KMB_FNS_UNIBA	ss3645302551	Oct 12, 2018 (152)
21	BIOINF_KMB_FNS_UNIBA	ss3645302552	Oct 12, 2018 (152)
22	URBANLAB	ss3650034519	Oct 12, 2018 (152)
23	EVA_DECODE	ss3695305457	Jul 13, 2019 (153)
24	EVA_DECODE	ss3695305458	Jul 13, 2019 (153)
25	EVA_DECODE	ss3695305459	Jul 13, 2019 (153)
26	ACPOP	ss3739753205	Jul 13, 2019 (153)
27	ACPOP	ss3739753206	Jul 13, 2019 (153)
28	PACBIO	ss3787460832	Jul 13, 2019 (153)
29	PACBIO	ss3792526362	Jul 13, 2019 (153)
30	PACBIO	ss3797410181	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3816803270	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3816803271	Jul 13, 2019 (153)
33	EVA	ss3833550569	Apr 27, 2020 (154)
34	EVA	ss3840356807	Apr 27, 2020 (154)
35	EVA	ss3845842672	Apr 27, 2020 (154)
36	KOGIC	ss3973577886	Apr 27, 2020 (154)
37	KOGIC	ss3973577887	Apr 27, 2020 (154)
38	KOGIC	ss3973577888	Apr 27, 2020 (154)
39	FSA-LAB	ss3984047127	Apr 26, 2021 (155)
40	GNOMAD	ss4265960815	Apr 26, 2021 (155)
41	GNOMAD	ss4265960816	Apr 26, 2021 (155)
42	GNOMAD	ss4265960818	Apr 26, 2021 (155)
43	GNOMAD	ss4265960819	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5210026444	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5210026445	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5210026446	Apr 26, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5293757016	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5293757017	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5293757018	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5488118782	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5488118783	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5761910771	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5761910772	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5761910773	Oct 16, 2022 (156)
55	EVA	ss5839486680	Oct 16, 2022 (156)
56	EVA	ss5839486681	Oct 16, 2022 (156)
57	1000Genomes	NC_000013.10 - 51939528	Oct 12, 2018 (152)
58	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33960536 (NC_000013.10:51939527:T: 744/3854) Row 33960537 (NC_000013.10:51939527::T 852/3854)	-	Oct 12, 2018 (152)
59	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33960536 (NC_000013.10:51939527:T: 744/3854) Row 33960537 (NC_000013.10:51939527::T 852/3854)	-	Oct 12, 2018 (152)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 430915054 (NC_000013.11:51365391::T 21886/137330) Row 430915055 (NC_000013.11:51365391::TT 15/137394) Row 430915057 (NC_000013.11:51365391:T: 25928/137300)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 430915054 (NC_000013.11:51365391::T 21886/137330) Row 430915055 (NC_000013.11:51365391::TT 15/137394) Row 430915057 (NC_000013.11:51365391:T: 25928/137300)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 430915054 (NC_000013.11:51365391::T 21886/137330) Row 430915055 (NC_000013.11:51365391::TT 15/137394) Row 430915057 (NC_000013.11:51365391:T: 25928/137300)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 430915054 (NC_000013.11:51365391::T 21886/137330) Row 430915055 (NC_000013.11:51365391::TT 15/137394) Row 430915057 (NC_000013.11:51365391:T: 25928/137300)...	-	Apr 26, 2021 (155)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 29955887 (NC_000013.11:51365392::T 183/1832) Row 29955888 (NC_000013.11:51365392::TT 4/1832) Row 29955889 (NC_000013.11:51365391:T: 531/1832)	-	Apr 27, 2020 (154)
65	Korean Genome Project Submission ignored due to conflicting rows: Row 29955887 (NC_000013.11:51365392::T 183/1832) Row 29955888 (NC_000013.11:51365392::TT 4/1832) Row 29955889 (NC_000013.11:51365391:T: 531/1832)	-	Apr 27, 2020 (154)
66	Korean Genome Project Submission ignored due to conflicting rows: Row 29955887 (NC_000013.11:51365392::T 183/1832) Row 29955888 (NC_000013.11:51365392::TT 4/1832) Row 29955889 (NC_000013.11:51365391:T: 531/1832)	-	Apr 27, 2020 (154)
67	Northern Sweden Submission ignored due to conflicting rows: Row 13038070 (NC_000013.10:51939527::T 131/600) Row 13038071 (NC_000013.10:51939527:T: 79/600)	-	Jul 13, 2019 (153)
68	Northern Sweden Submission ignored due to conflicting rows: Row 13038070 (NC_000013.10:51939527::T 131/600) Row 13038071 (NC_000013.10:51939527:T: 79/600)	-	Jul 13, 2019 (153)
69	8.3KJPN Submission ignored due to conflicting rows: Row 67995751 (NC_000013.10:51939527:T: 5189/16760) Row 67995752 (NC_000013.10:51939527::T 2584/16760) Row 67995753 (NC_000013.10:51939527::TT 143/16760)	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 67995751 (NC_000013.10:51939527:T: 5189/16760) Row 67995752 (NC_000013.10:51939527::T 2584/16760) Row 67995753 (NC_000013.10:51939527::TT 143/16760)	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 67995751 (NC_000013.10:51939527:T: 5189/16760) Row 67995752 (NC_000013.10:51939527::T 2584/16760) Row 67995753 (NC_000013.10:51939527::TT 143/16760)	-	Apr 26, 2021 (155)
72	14KJPN Submission ignored due to conflicting rows: Row 95747875 (NC_000013.11:51365391:T: 8735/28258) Row 95747876 (NC_000013.11:51365391::T 4414/28258) Row 95747877 (NC_000013.11:51365391::TT 223/28258)	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 95747875 (NC_000013.11:51365391:T: 8735/28258) Row 95747876 (NC_000013.11:51365391::T 4414/28258) Row 95747877 (NC_000013.11:51365391::TT 223/28258)	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 95747875 (NC_000013.11:51365391:T: 8735/28258) Row 95747876 (NC_000013.11:51365391::T 4414/28258) Row 95747877 (NC_000013.11:51365391::TT 223/28258)	-	Oct 16, 2022 (156)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33960536 (NC_000013.10:51939527:T: 719/3708) Row 33960537 (NC_000013.10:51939527::T 824/3708)	-	Oct 12, 2018 (152)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33960536 (NC_000013.10:51939527:T: 719/3708) Row 33960537 (NC_000013.10:51939527::T 824/3708)	-	Oct 12, 2018 (152)
77	ALFA	NC_000013.11 - 51365392	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)
rs374749917	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4265960819	NC_000013.11:51365391:TTTT:	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTT	(self)
6969441961	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTT	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTT	(self)
6969441961	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTT	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTT	(self)
ss289177914, ss327526909, ss328074474, ss552600198, ss553519555	NC_000013.9:50837528:T:	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTT	(self)
61121036, ss664181422, ss666599371, ss1373167708, ss1707788876, ss1707789015, ss2628312375, ss3739753206, ss3787460832, ss3792526362, ss3797410181, ss3833550569, ss5210026444, ss5839486680	NC_000013.10:51939527:T:	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTT	(self)
ss3645302552, ss3650034519, ss3695305457, ss3816803271, ss3973577888, ss4265960818, ss5293757017, ss5488118782, ss5761910771	NC_000013.11:51365391:T:	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTT	(self)
6969441961	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTT	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTT	(self)
ss327628673, ss552293017	NC_000013.9:50837528::T	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss289177915	NC_000013.9:50837538::T	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3739753205, ss3840356807, ss3984047127, ss5210026445, ss5839486681	NC_000013.10:51939527::T	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss1373167711, ss1710602394, ss1710602401, ss1997060616	NC_000013.10:51939528::T	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3064596482, ss3645302551, ss3845842672, ss4265960815, ss5293757016, ss5488118783, ss5761910772	NC_000013.11:51365391::T	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTT	(self)
6969441961	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTT	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3695305458, ss3816803270, ss3973577886	NC_000013.11:51365392::T	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss5210026446	NC_000013.10:51939527::TT	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4265960816, ss5293757018, ss5761910773	NC_000013.11:51365391::TT	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTTT	(self)
6969441961	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTTT	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3973577887	NC_000013.11:51365392::TT	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3695305459	NC_000013.11:51365392::TTTTTTTTTTT	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3192858133	NC_000013.11:51365391:TTT:	NC_000013.11:51365391:TTTTTTTTTT:T… NC_000013.11:51365391:TTTTTTTTTT:TTTTTTT

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

No publications for rs149255221

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

rs149255221