Name: rs71513356
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.

rs71513356

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:13165876-13165892 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.1699 (851/5008, 1000G)
delAAA=0.0000 (0/3214, ALFA)
delAA=0.0000 (0/3214, ALFA) (+ 6 more)
delA=0.0000 (0/3214, ALFA)
dupA=0.0000 (0/3214, ALFA)
dupAA=0.0000 (0/3214, ALFA)
dupAAA=0.0000 (0/3214, ALFA)
dup(A)₄=0.0000 (0/3214, ALFA)
dup(A)₅=0.0000 (0/3214, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MCM10 : 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	3214	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2170	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	618	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	16	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	602	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	38	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	30	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	8	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	34	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	204	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	34	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	116	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₁₇=0.8301	delA=0.1699
1000Genomes	African	Sub	1322	(A)₁₇=0.8744	delA=0.1256
1000Genomes	East Asian	Sub	1008	(A)₁₇=0.8254	delA=0.1746
1000Genomes	Europe	Sub	1006	(A)₁₇=0.8260	delA=0.1740
1000Genomes	South Asian	Sub	978	(A)₁₇=0.812	delA=0.188
1000Genomes	American	Sub	694	(A)₁₇=0.784	delA=0.216
Allele Frequency Aggregator	Total	Global	3214	(A)₁₇=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	2170	(A)₁₇=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	African	Sub	618	(A)₁₇=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	204	(A)₁₇=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	116	(A)₁₇=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Asian	Sub	38	(A)₁₇=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	34	(A)₁₇=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	34	(A)₁₇=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 10	NC_000010.11:g.13165890_13165892del
GRCh38.p14 chr 10	NC_000010.11:g.13165891_13165892del
GRCh38.p14 chr 10	NC_000010.11:g.13165892del
GRCh38.p14 chr 10	NC_000010.11:g.13165892dup
GRCh38.p14 chr 10	NC_000010.11:g.13165891_13165892dup
GRCh38.p14 chr 10	NC_000010.11:g.13165890_13165892dup
GRCh38.p14 chr 10	NC_000010.11:g.13165889_13165892dup
GRCh38.p14 chr 10	NC_000010.11:g.13165888_13165892dup
GRCh37.p13 chr 10	NC_000010.10:g.13207890_13207892del
GRCh37.p13 chr 10	NC_000010.10:g.13207891_13207892del
GRCh37.p13 chr 10	NC_000010.10:g.13207892del
GRCh37.p13 chr 10	NC_000010.10:g.13207892dup
GRCh37.p13 chr 10	NC_000010.10:g.13207891_13207892dup
GRCh37.p13 chr 10	NC_000010.10:g.13207890_13207892dup
GRCh37.p13 chr 10	NC_000010.10:g.13207889_13207892dup
GRCh37.p13 chr 10	NC_000010.10:g.13207888_13207892dup

Gene: MCM10, minichromosome maintenance 10 replication initiation factor (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MCM10 transcript variant 2	NM_018518.5:c.7+1681_7+16… NM_018518.5:c.7+1681_7+1683del	N/A	Intron Variant
MCM10 transcript variant 1	NM_182751.3:c.7+1681_7+16… NM_182751.3:c.7+1681_7+1683del	N/A	Intron Variant
MCM10 transcript variant X1	XM_011519538.3:c.7+1681_7… XM_011519538.3:c.7+1681_7+1683del	N/A	Intron Variant
MCM10 transcript variant X2	XM_047425437.1:c.7+1681_7… XM_047425437.1:c.7+1681_7+1683del	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	(A)₁₇=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅
GRCh38.p14 chr 10	NC_000010.11:g.13165876_13165892=	NC_000010.11:g.13165890_13165892del	NC_000010.11:g.13165891_13165892del	NC_000010.11:g.13165892del	NC_000010.11:g.13165892dup	NC_000010.11:g.13165891_13165892dup	NC_000010.11:g.13165890_13165892dup	NC_000010.11:g.13165889_13165892dup	NC_000010.11:g.13165888_13165892dup
GRCh37.p13 chr 10	NC_000010.10:g.13207876_13207892=	NC_000010.10:g.13207890_13207892del	NC_000010.10:g.13207891_13207892del	NC_000010.10:g.13207892del	NC_000010.10:g.13207892dup	NC_000010.10:g.13207891_13207892dup	NC_000010.10:g.13207890_13207892dup	NC_000010.10:g.13207889_13207892dup	NC_000010.10:g.13207888_13207892dup
MCM10 transcript variant 2	NM_018518.4:c.7+1667=	NM_018518.4:c.7+1681_7+1683del	NM_018518.4:c.7+1682_7+1683del	NM_018518.4:c.7+1683del	NM_018518.4:c.7+1683dup	NM_018518.4:c.7+1682_7+1683dup	NM_018518.4:c.7+1681_7+1683dup	NM_018518.4:c.7+1680_7+1683dup	NM_018518.4:c.7+1679_7+1683dup
MCM10 transcript variant 2	NM_018518.5:c.7+1667=	NM_018518.5:c.7+1681_7+1683del	NM_018518.5:c.7+1682_7+1683del	NM_018518.5:c.7+1683del	NM_018518.5:c.7+1683dup	NM_018518.5:c.7+1682_7+1683dup	NM_018518.5:c.7+1681_7+1683dup	NM_018518.5:c.7+1680_7+1683dup	NM_018518.5:c.7+1679_7+1683dup
MCM10 transcript variant 1	NM_182751.2:c.7+1667=	NM_182751.2:c.7+1681_7+1683del	NM_182751.2:c.7+1682_7+1683del	NM_182751.2:c.7+1683del	NM_182751.2:c.7+1683dup	NM_182751.2:c.7+1682_7+1683dup	NM_182751.2:c.7+1681_7+1683dup	NM_182751.2:c.7+1680_7+1683dup	NM_182751.2:c.7+1679_7+1683dup
MCM10 transcript variant 1	NM_182751.3:c.7+1667=	NM_182751.3:c.7+1681_7+1683del	NM_182751.3:c.7+1682_7+1683del	NM_182751.3:c.7+1683del	NM_182751.3:c.7+1683dup	NM_182751.3:c.7+1682_7+1683dup	NM_182751.3:c.7+1681_7+1683dup	NM_182751.3:c.7+1680_7+1683dup	NM_182751.3:c.7+1679_7+1683dup
MCM10 transcript variant X1	XM_011519538.3:c.7+1667=	XM_011519538.3:c.7+1681_7+1683del	XM_011519538.3:c.7+1682_7+1683del	XM_011519538.3:c.7+1683del	XM_011519538.3:c.7+1683dup	XM_011519538.3:c.7+1682_7+1683dup	XM_011519538.3:c.7+1681_7+1683dup	XM_011519538.3:c.7+1680_7+1683dup	XM_011519538.3:c.7+1679_7+1683dup
MCM10 transcript variant X2	XM_047425437.1:c.7+1667=	XM_047425437.1:c.7+1681_7+1683del	XM_047425437.1:c.7+1682_7+1683del	XM_047425437.1:c.7+1683del	XM_047425437.1:c.7+1683dup	XM_047425437.1:c.7+1682_7+1683dup	XM_047425437.1:c.7+1681_7+1683dup	XM_047425437.1:c.7+1680_7+1683dup	XM_047425437.1:c.7+1679_7+1683dup

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#.

51 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss97600387	Feb 13, 2009 (130)
2	PJP	ss294643178	May 09, 2011 (137)
3	PJP	ss294643179	May 09, 2011 (137)
4	SSMP	ss663963923	Apr 01, 2015 (144)
5	1000GENOMES	ss1369136394	Aug 21, 2014 (142)
6	SWEGEN	ss3005967874	Nov 08, 2017 (151)
7	MCHAISSO	ss3065368432	Nov 17, 2017 (151)
8	URBANLAB	ss3649295580	Oct 12, 2018 (152)
9	EVA_DECODE	ss3689319225	Jul 13, 2019 (153)
10	EVA_DECODE	ss3689319226	Jul 13, 2019 (153)
11	EVA_DECODE	ss3689319227	Jul 13, 2019 (153)
12	EVA_DECODE	ss3689319228	Jul 13, 2019 (153)
13	EVA_DECODE	ss3689319229	Jul 13, 2019 (153)
14	PACBIO	ss3786588834	Jul 13, 2019 (153)
15	PACBIO	ss3791780776	Jul 13, 2019 (153)
16	PACBIO	ss3791780777	Jul 13, 2019 (153)
17	PACBIO	ss3796662637	Jul 13, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3813130854	Jul 13, 2019 (153)
19	EVA	ss3831978803	Apr 26, 2020 (154)
20	EVA	ss3839521039	Apr 26, 2020 (154)
21	EVA	ss3844987506	Apr 26, 2020 (154)
22	KOGIC	ss3967238811	Apr 26, 2020 (154)
23	KOGIC	ss3967238812	Apr 26, 2020 (154)
24	KOGIC	ss3967238813	Apr 26, 2020 (154)
25	KOGIC	ss3967238814	Apr 26, 2020 (154)
26	GNOMAD	ss4213222268	Apr 26, 2021 (155)
27	GNOMAD	ss4213222269	Apr 26, 2021 (155)
28	GNOMAD	ss4213222270	Apr 26, 2021 (155)
29	GNOMAD	ss4213222271	Apr 26, 2021 (155)
30	GNOMAD	ss4213222272	Apr 26, 2021 (155)
31	GNOMAD	ss4213222273	Apr 26, 2021 (155)
32	GNOMAD	ss4213222274	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5196346415	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5196346416	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5196346417	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5196346418	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5196346419	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5282983704	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5282983705	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5282983706	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5282983707	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5478754534	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5478754535	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5478754536	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5478754537	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5478754538	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5741219063	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5741219064	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5741219065	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5741219066	Oct 16, 2022 (156)
51	EVA	ss5980596696	Oct 16, 2022 (156)
52	1000Genomes	NC_000010.10 - 13207876	Oct 12, 2018 (152)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343943112 (NC_000010.11:13165875::A 5118/100190) Row 343943113 (NC_000010.11:13165875::AA 38520/99658) Row 343943114 (NC_000010.11:13165875::AAA 1231/100128)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343943112 (NC_000010.11:13165875::A 5118/100190) Row 343943113 (NC_000010.11:13165875::AA 38520/99658) Row 343943114 (NC_000010.11:13165875::AAA 1231/100128)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343943112 (NC_000010.11:13165875::A 5118/100190) Row 343943113 (NC_000010.11:13165875::AA 38520/99658) Row 343943114 (NC_000010.11:13165875::AAA 1231/100128)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343943112 (NC_000010.11:13165875::A 5118/100190) Row 343943113 (NC_000010.11:13165875::AA 38520/99658) Row 343943114 (NC_000010.11:13165875::AAA 1231/100128)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343943112 (NC_000010.11:13165875::A 5118/100190) Row 343943113 (NC_000010.11:13165875::AA 38520/99658) Row 343943114 (NC_000010.11:13165875::AAA 1231/100128)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343943112 (NC_000010.11:13165875::A 5118/100190) Row 343943113 (NC_000010.11:13165875::AA 38520/99658) Row 343943114 (NC_000010.11:13165875::AAA 1231/100128)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 343943112 (NC_000010.11:13165875::A 5118/100190) Row 343943113 (NC_000010.11:13165875::AA 38520/99658) Row 343943114 (NC_000010.11:13165875::AAA 1231/100128)...	-	Apr 26, 2021 (155)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 23616812 (NC_000010.11:13165876::AA 627/1818) Row 23616813 (NC_000010.11:13165876::AAA 55/1818) Row 23616814 (NC_000010.11:13165875:A: 145/1818)...	-	Apr 26, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 23616812 (NC_000010.11:13165876::AA 627/1818) Row 23616813 (NC_000010.11:13165876::AAA 55/1818) Row 23616814 (NC_000010.11:13165875:A: 145/1818)...	-	Apr 26, 2020 (154)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 23616812 (NC_000010.11:13165876::AA 627/1818) Row 23616813 (NC_000010.11:13165876::AAA 55/1818) Row 23616814 (NC_000010.11:13165875:A: 145/1818)...	-	Apr 26, 2020 (154)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 23616812 (NC_000010.11:13165876::AA 627/1818) Row 23616813 (NC_000010.11:13165876::AAA 55/1818) Row 23616814 (NC_000010.11:13165875:A: 145/1818)...	-	Apr 26, 2020 (154)
64	8.3KJPN Submission ignored due to conflicting rows: Row 54315722 (NC_000010.10:13207875::AA 5870/16586) Row 54315723 (NC_000010.10:13207875:A: 570/16586) Row 54315724 (NC_000010.10:13207875::A 165/16586)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 54315722 (NC_000010.10:13207875::AA 5870/16586) Row 54315723 (NC_000010.10:13207875:A: 570/16586) Row 54315724 (NC_000010.10:13207875::A 165/16586)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 54315722 (NC_000010.10:13207875::AA 5870/16586) Row 54315723 (NC_000010.10:13207875:A: 570/16586) Row 54315724 (NC_000010.10:13207875::A 165/16586)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 54315722 (NC_000010.10:13207875::AA 5870/16586) Row 54315723 (NC_000010.10:13207875:A: 570/16586) Row 54315724 (NC_000010.10:13207875::A 165/16586)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 54315722 (NC_000010.10:13207875::AA 5870/16586) Row 54315723 (NC_000010.10:13207875:A: 570/16586) Row 54315724 (NC_000010.10:13207875::A 165/16586)...	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 75056167 (NC_000010.11:13165875::AA 9411/28102) Row 75056168 (NC_000010.11:13165875::A 230/28102) Row 75056169 (NC_000010.11:13165875:A: 979/28102)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 75056167 (NC_000010.11:13165875::AA 9411/28102) Row 75056168 (NC_000010.11:13165875::A 230/28102) Row 75056169 (NC_000010.11:13165875:A: 979/28102)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 75056167 (NC_000010.11:13165875::AA 9411/28102) Row 75056168 (NC_000010.11:13165875::A 230/28102) Row 75056169 (NC_000010.11:13165875:A: 979/28102)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 75056167 (NC_000010.11:13165875::AA 9411/28102) Row 75056168 (NC_000010.11:13165875::A 230/28102) Row 75056169 (NC_000010.11:13165875:A: 979/28102)...	-	Oct 16, 2022 (156)
73	ALFA	NC_000010.11 - 13165876	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)
rs72281890	May 11, 2012 (137)
rs146353296	May 11, 2012 (137)
rs147879935	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11458806418	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3065368432, ss3689319229, ss4213222274, ss5478754534	NC_000010.11:13165875:AA:	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
11458806418	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
48696267, ss1369136394, ss3005967874, ss3839521039, ss5196346416	NC_000010.10:13207875:A:	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3813130854, ss3844987506, ss3967238813, ss4213222273, ss5282983704, ss5478754535, ss5741219065	NC_000010.11:13165875:A:	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
11458806418	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3689319228	NC_000010.11:13165876:A:	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3786588834, ss3791780776, ss3796662637, ss5196346417	NC_000010.10:13207875::A	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4213222268, ss5282983707, ss5478754537, ss5741219064	NC_000010.11:13165875::A	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
11458806418	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3967238814	NC_000010.11:13165876::A	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3689319227	NC_000010.11:13165877::A	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss294643178	NC_000010.9:13247882::AA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294643179	NC_000010.9:13247897::AA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss663963923, ss3791780777, ss3831978803, ss5196346415, ss5980596696	NC_000010.10:13207875::AA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3649295580, ss4213222269, ss5282983705, ss5478754536, ss5741219063	NC_000010.11:13165875::AA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
11458806418	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3967238811	NC_000010.11:13165876::AA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3689319226	NC_000010.11:13165877::AA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss97600387	NT_008705.16:13147892::AA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5196346418	NC_000010.10:13207875::AAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4213222270, ss5282983706, ss5478754538, ss5741219066	NC_000010.11:13165875::AAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
11458806418	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3967238812	NC_000010.11:13165876::AAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3689319225	NC_000010.11:13165877::AAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5196346419	NC_000010.10:13207875::AAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4213222271	NC_000010.11:13165875::AAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
11458806418	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4213222272	NC_000010.11:13165875::AAAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
11458806418	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:13165875:AAAAAAAAAAAA… NC_000010.11:13165875:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(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 rs71513356

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

rs71513356