Name: rs71010904
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.

rs71010904

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:6598788-6598801 (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)₅ / delTTT / delTT / delT / …
del(T)₅ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₅=0.0000 (0/3810, ALFA)
delTTT=0.0000 (0/3810, ALFA)
delTT=0.0000 (0/3810, ALFA) (+ 4 more)
delT=0.0000 (0/3810, ALFA)
dupT=0.0000 (0/3810, ALFA)
dupTT=0.0000 (0/3810, ALFA)
dupT=0.010 (4/396, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: INTS15 : 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	3810	TTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	3142	TTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	234	TTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A
African Others	Sub	6	TTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0	1.0	N/A
African American	Sub	228	TTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A
Asian	Sub	58	TTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	46	TTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	12	TTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	36	TTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	162	TTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	32	TTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	146	TTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=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	3810	(T)₁₄=1.0000	del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	3142	(T)₁₄=1.0000	del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	234	(T)₁₄=1.000	del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	162	(T)₁₄=1.000	del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	146	(T)₁₄=1.000	del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Asian	Sub	58	(T)₁₄=1.00	del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	36	(T)₁₄=1.00	del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(T)₁₄=1.00	del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Northern Sweden	ACPOP	Study-wide	396	- No frequency provided	dupT=0.010

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 7	NC_000007.14:g.6598797_6598801del
GRCh38.p14 chr 7	NC_000007.14:g.6598799_6598801del
GRCh38.p14 chr 7	NC_000007.14:g.6598800_6598801del
GRCh38.p14 chr 7	NC_000007.14:g.6598801del
GRCh38.p14 chr 7	NC_000007.14:g.6598801dup
GRCh38.p14 chr 7	NC_000007.14:g.6598800_6598801dup
GRCh38.p14 chr 7	NC_000007.14:g.6598799_6598801dup
GRCh38.p14 chr 7	NC_000007.14:g.6598794_6598801dup
GRCh37.p13 chr 7	NC_000007.13:g.6638428_6638432del
GRCh37.p13 chr 7	NC_000007.13:g.6638430_6638432del
GRCh37.p13 chr 7	NC_000007.13:g.6638431_6638432del
GRCh37.p13 chr 7	NC_000007.13:g.6638432del
GRCh37.p13 chr 7	NC_000007.13:g.6638432dup
GRCh37.p13 chr 7	NC_000007.13:g.6638431_6638432dup
GRCh37.p13 chr 7	NC_000007.13:g.6638430_6638432dup
GRCh37.p13 chr 7	NC_000007.13:g.6638425_6638432dup

Gene: INTS15, integrator complex subunit 15 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
INTS15 transcript variant 2	NM_001303039.2:c.524-1032… NM_001303039.2:c.524-1032_524-1028del	N/A	Intron Variant
INTS15 transcript variant 1	NM_024067.4:c.581-1032_58… NM_024067.4:c.581-1032_581-1028del	N/A	Intron Variant
INTS15 transcript variant X1	XM_005249845.6:c.581-1032… XM_005249845.6:c.581-1032_581-1028del	N/A	Intron Variant
INTS15 transcript variant X2	XM_011515518.4:c.581-1032… XM_011515518.4:c.581-1032_581-1028del	N/A	Intron Variant
INTS15 transcript variant X3	XM_017012614.3:c.251-1032… XM_017012614.3:c.251-1032_251-1028del	N/A	Intron Variant
INTS15 transcript variant X5	XM_047420833.1:c.581-1032… XM_047420833.1:c.581-1032_581-1028del	N/A	Intron Variant
INTS15 transcript variant X4	XR_926946.4: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)₅	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₈
GRCh38.p14 chr 7	NC_000007.14:g.6598788_6598801=	NC_000007.14:g.6598797_6598801del	NC_000007.14:g.6598799_6598801del	NC_000007.14:g.6598800_6598801del	NC_000007.14:g.6598801del	NC_000007.14:g.6598801dup	NC_000007.14:g.6598800_6598801dup	NC_000007.14:g.6598799_6598801dup	NC_000007.14:g.6598794_6598801dup
GRCh37.p13 chr 7	NC_000007.13:g.6638419_6638432=	NC_000007.13:g.6638428_6638432del	NC_000007.13:g.6638430_6638432del	NC_000007.13:g.6638431_6638432del	NC_000007.13:g.6638432del	NC_000007.13:g.6638432dup	NC_000007.13:g.6638431_6638432dup	NC_000007.13:g.6638430_6638432dup	NC_000007.13:g.6638425_6638432dup
INTS15 transcript variant 2	NM_001303039.2:c.524-1041=	NM_001303039.2:c.524-1032_524-1028del	NM_001303039.2:c.524-1030_524-1028del	NM_001303039.2:c.524-1029_524-1028del	NM_001303039.2:c.524-1028del	NM_001303039.2:c.524-1028dup	NM_001303039.2:c.524-1029_524-1028dup	NM_001303039.2:c.524-1030_524-1028dup	NM_001303039.2:c.524-1035_524-1028dup
C7orf26 transcript	NM_024067.2:c.581-1041=	NM_024067.2:c.581-1032_581-1028del	NM_024067.2:c.581-1030_581-1028del	NM_024067.2:c.581-1029_581-1028del	NM_024067.2:c.581-1028del	NM_024067.2:c.581-1028dup	NM_024067.2:c.581-1029_581-1028dup	NM_024067.2:c.581-1030_581-1028dup	NM_024067.2:c.581-1035_581-1028dup
INTS15 transcript variant 1	NM_024067.4:c.581-1041=	NM_024067.4:c.581-1032_581-1028del	NM_024067.4:c.581-1030_581-1028del	NM_024067.4:c.581-1029_581-1028del	NM_024067.4:c.581-1028del	NM_024067.4:c.581-1028dup	NM_024067.4:c.581-1029_581-1028dup	NM_024067.4:c.581-1030_581-1028dup	NM_024067.4:c.581-1035_581-1028dup
C7orf26 transcript variant X1	XM_005249845.1:c.581-1041=	XM_005249845.1:c.581-1032_581-1028del	XM_005249845.1:c.581-1030_581-1028del	XM_005249845.1:c.581-1029_581-1028del	XM_005249845.1:c.581-1028del	XM_005249845.1:c.581-1028dup	XM_005249845.1:c.581-1029_581-1028dup	XM_005249845.1:c.581-1030_581-1028dup	XM_005249845.1:c.581-1035_581-1028dup
INTS15 transcript variant X1	XM_005249845.6:c.581-1041=	XM_005249845.6:c.581-1032_581-1028del	XM_005249845.6:c.581-1030_581-1028del	XM_005249845.6:c.581-1029_581-1028del	XM_005249845.6:c.581-1028del	XM_005249845.6:c.581-1028dup	XM_005249845.6:c.581-1029_581-1028dup	XM_005249845.6:c.581-1030_581-1028dup	XM_005249845.6:c.581-1035_581-1028dup
C7orf26 transcript variant X2	XM_005249846.1:c.524-1041=	XM_005249846.1:c.524-1032_524-1028del	XM_005249846.1:c.524-1030_524-1028del	XM_005249846.1:c.524-1029_524-1028del	XM_005249846.1:c.524-1028del	XM_005249846.1:c.524-1028dup	XM_005249846.1:c.524-1029_524-1028dup	XM_005249846.1:c.524-1030_524-1028dup	XM_005249846.1:c.524-1035_524-1028dup
INTS15 transcript variant X2	XM_011515518.4:c.581-1041=	XM_011515518.4:c.581-1032_581-1028del	XM_011515518.4:c.581-1030_581-1028del	XM_011515518.4:c.581-1029_581-1028del	XM_011515518.4:c.581-1028del	XM_011515518.4:c.581-1028dup	XM_011515518.4:c.581-1029_581-1028dup	XM_011515518.4:c.581-1030_581-1028dup	XM_011515518.4:c.581-1035_581-1028dup
INTS15 transcript variant X3	XM_017012614.3:c.251-1041=	XM_017012614.3:c.251-1032_251-1028del	XM_017012614.3:c.251-1030_251-1028del	XM_017012614.3:c.251-1029_251-1028del	XM_017012614.3:c.251-1028del	XM_017012614.3:c.251-1028dup	XM_017012614.3:c.251-1029_251-1028dup	XM_017012614.3:c.251-1030_251-1028dup	XM_017012614.3:c.251-1035_251-1028dup
INTS15 transcript variant X5	XM_047420833.1:c.581-1041=	XM_047420833.1:c.581-1032_581-1028del	XM_047420833.1:c.581-1030_581-1028del	XM_047420833.1:c.581-1029_581-1028del	XM_047420833.1:c.581-1028del	XM_047420833.1:c.581-1028dup	XM_047420833.1:c.581-1029_581-1028dup	XM_047420833.1:c.581-1030_581-1028dup	XM_047420833.1:c.581-1035_581-1028dup

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#.

37 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95451485	Feb 13, 2009 (130)
2	BUSHMAN	ss193904225	Mar 15, 2016 (147)
3	PJP	ss295322813	May 09, 2011 (137)
4	BILGI_BIOE	ss666385911	Apr 25, 2013 (138)
5	EVA_DECODE	ss3719007073	Jul 13, 2019 (153)
6	EVA_DECODE	ss3719007075	Jul 13, 2019 (153)
7	EVA_DECODE	ss3719007076	Jul 13, 2019 (153)
8	EVA_DECODE	ss3719007077	Jul 13, 2019 (153)
9	ACPOP	ss3734311544	Jul 13, 2019 (153)
10	PACBIO	ss3785719563	Jul 13, 2019 (153)
11	PACBIO	ss3791035178	Jul 13, 2019 (153)
12	PACBIO	ss3795914890	Jul 13, 2019 (153)
13	EVA	ss3830385464	Apr 26, 2020 (154)
14	EVA	ss3838679425	Apr 26, 2020 (154)
15	KOGIC	ss3960799304	Apr 26, 2020 (154)
16	KOGIC	ss3960799305	Apr 26, 2020 (154)
17	KOGIC	ss3960799306	Apr 26, 2020 (154)
18	GNOMAD	ss4157567140	Apr 26, 2021 (155)
19	GNOMAD	ss4157567143	Apr 26, 2021 (155)
20	GNOMAD	ss4157567144	Apr 26, 2021 (155)
21	GNOMAD	ss4157567147	Apr 26, 2021 (155)
22	GNOMAD	ss4157567148	Apr 26, 2021 (155)
23	GNOMAD	ss4157567149	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5181605158	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5181605159	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5181605160	Apr 26, 2021 (155)
27	1000G_HIGH_COVERAGE	ss5271656462	Oct 13, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5271656465	Oct 13, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5271656466	Oct 13, 2022 (156)
30	HUGCELL_USP	ss5468961834	Oct 13, 2022 (156)
31	HUGCELL_USP	ss5468961836	Oct 13, 2022 (156)
32	HUGCELL_USP	ss5468961838	Oct 13, 2022 (156)
33	TOMMO_GENOMICS	ss5721002084	Oct 13, 2022 (156)
34	TOMMO_GENOMICS	ss5721002085	Oct 13, 2022 (156)
35	TOMMO_GENOMICS	ss5721002086	Oct 13, 2022 (156)
36	EVA	ss5822340443	Oct 13, 2022 (156)
37	EVA	ss5822340444	Oct 13, 2022 (156)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251530373 (NC_000007.14:6598787::T 32884/64912) Row 251530376 (NC_000007.14:6598787::TT 79/64898) Row 251530377 (NC_000007.14:6598787::TTT 1/64898)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251530373 (NC_000007.14:6598787::T 32884/64912) Row 251530376 (NC_000007.14:6598787::TT 79/64898) Row 251530377 (NC_000007.14:6598787::TTT 1/64898)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251530373 (NC_000007.14:6598787::T 32884/64912) Row 251530376 (NC_000007.14:6598787::TT 79/64898) Row 251530377 (NC_000007.14:6598787::TTT 1/64898)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251530373 (NC_000007.14:6598787::T 32884/64912) Row 251530376 (NC_000007.14:6598787::TT 79/64898) Row 251530377 (NC_000007.14:6598787::TTT 1/64898)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251530373 (NC_000007.14:6598787::T 32884/64912) Row 251530376 (NC_000007.14:6598787::TT 79/64898) Row 251530377 (NC_000007.14:6598787::TTT 1/64898)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251530373 (NC_000007.14:6598787::T 32884/64912) Row 251530376 (NC_000007.14:6598787::TT 79/64898) Row 251530377 (NC_000007.14:6598787::TTT 1/64898)...	-	Apr 26, 2021 (155)
44	Korean Genome Project Submission ignored due to conflicting rows: Row 17177305 (NC_000007.14:6598791::T 218/1658) Row 17177306 (NC_000007.14:6598790:T: 28/1658) Row 17177307 (NC_000007.14:6598789:TT: 8/1658)	-	Apr 26, 2020 (154)
45	Korean Genome Project Submission ignored due to conflicting rows: Row 17177305 (NC_000007.14:6598791::T 218/1658) Row 17177306 (NC_000007.14:6598790:T: 28/1658) Row 17177307 (NC_000007.14:6598789:TT: 8/1658)	-	Apr 26, 2020 (154)
46	Korean Genome Project Submission ignored due to conflicting rows: Row 17177305 (NC_000007.14:6598791::T 218/1658) Row 17177306 (NC_000007.14:6598790:T: 28/1658) Row 17177307 (NC_000007.14:6598789:TT: 8/1658)	-	Apr 26, 2020 (154)
47	Northern Sweden	NC_000007.13 - 6638419	Jul 13, 2019 (153)
48	8.3KJPN Submission ignored due to conflicting rows: Row 39574465 (NC_000007.13:6638418:T: 24/14510) Row 39574466 (NC_000007.13:6638418::T 1391/14510) Row 39574467 (NC_000007.13:6638418:TT: 41/14510)	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 39574465 (NC_000007.13:6638418:T: 24/14510) Row 39574466 (NC_000007.13:6638418::T 1391/14510) Row 39574467 (NC_000007.13:6638418:TT: 41/14510)	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 39574465 (NC_000007.13:6638418:T: 24/14510) Row 39574466 (NC_000007.13:6638418::T 1391/14510) Row 39574467 (NC_000007.13:6638418:TT: 41/14510)	-	Apr 26, 2021 (155)
51	14KJPN Submission ignored due to conflicting rows: Row 54839188 (NC_000007.14:6598787:T: 52/26598) Row 54839189 (NC_000007.14:6598787:TT: 71/26598) Row 54839190 (NC_000007.14:6598787::T 3146/26598)	-	Oct 13, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 54839188 (NC_000007.14:6598787:T: 52/26598) Row 54839189 (NC_000007.14:6598787:TT: 71/26598) Row 54839190 (NC_000007.14:6598787::T 3146/26598)	-	Oct 13, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 54839188 (NC_000007.14:6598787:T: 52/26598) Row 54839189 (NC_000007.14:6598787:TT: 71/26598) Row 54839190 (NC_000007.14:6598787::T 3146/26598)	-	Oct 13, 2022 (156)
54	ALFA	NC_000007.14 - 6598788	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)
rs112364030	May 11, 2012 (137)
rs72317592	May 11, 2012 (137)
rs72437552	May 11, 2012 (137)
rs143100686	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4157567149	NC_000007.14:6598787:TTTTT:	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTT	(self)
4586086005	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTT	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss5822340444	NC_000007.13:6638418:TTT:	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTT
4586086005	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5181605160	NC_000007.13:6638418:TT:	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4157567148, ss5721002085	NC_000007.14:6598787:TT:	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4586086005	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3960799306	NC_000007.14:6598789:TT:	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5181605158	NC_000007.13:6638418:T:	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3719007073, ss4157567147, ss5271656465, ss5468961834, ss5721002084	NC_000007.14:6598787:T:	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4586086005	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3960799305	NC_000007.14:6598790:T:	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss295322813	NC_000007.12:6604950::T	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7596409, ss666385911, ss3734311544, ss3785719563, ss3791035178, ss3795914890, ss3830385464, ss3838679425, ss5181605159, ss5822340443	NC_000007.13:6638418::T	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4157567140, ss5271656462, ss5468961836, ss5721002086	NC_000007.14:6598787::T	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4586086005	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3719007075	NC_000007.14:6598788::T	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3960799304	NC_000007.14:6598791::T	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss193904225	NT_007819.17:6628418::T	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss95451485	NT_007819.17:6628432::T	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4157567143, ss5271656466, ss5468961838	NC_000007.14:6598787::TT	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4586086005	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3719007076	NC_000007.14:6598788::TT	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4157567144	NC_000007.14:6598787::TTT	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3719007077	NC_000007.14:6598788::TTTTTTTT	NC_000007.14:6598787:TTTTTTTTTTTTT… NC_000007.14:6598787:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(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 rs71010904

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

rs71010904