Name: rs10523480
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.

rs10523480

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:70765736-70765750 (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 / dup(A)₉ / dup(A)₁₅ / ins(A)₉C(A)₁₅
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.0000 (0/2120, ALFA)
delAA=0.0000 (0/2120, ALFA)
delA=0.0000 (0/2120, ALFA) (+ 1 more)
dupA=0.0000 (0/2120, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MAP3K9 : 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	2120	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1510	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	368	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	18	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	350	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	18	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	16	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	12	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	130	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	8	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other	Sub	74	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	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
Allele Frequency Aggregator	Total	Global	2120	(A)₁₅=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	European	Sub	1510	(A)₁₅=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	African	Sub	368	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	130	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Other	Sub	74	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Asian	Sub	18	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	South Asian	Sub	8	(A)₁₅=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0

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.70765748_70765750del
GRCh38.p14 chr 14	NC_000014.9:g.70765749_70765750del
GRCh38.p14 chr 14	NC_000014.9:g.70765750del
GRCh38.p14 chr 14	NC_000014.9:g.70765750dup
GRCh38.p14 chr 14	NC_000014.9:g.70765749_70765750dup
GRCh38.p14 chr 14	NC_000014.9:g.70765742_70765750dup
GRCh38.p14 chr 14	NC_000014.9:g.70765736_70765750dup
GRCh38.p14 chr 14	NC_000014.9:g.70765736_70765750A[24]CAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 14	NC_000014.8:g.71232465_71232467del
GRCh37.p13 chr 14	NC_000014.8:g.71232466_71232467del
GRCh37.p13 chr 14	NC_000014.8:g.71232467del
GRCh37.p13 chr 14	NC_000014.8:g.71232467dup
GRCh37.p13 chr 14	NC_000014.8:g.71232466_71232467dup
GRCh37.p13 chr 14	NC_000014.8:g.71232459_71232467dup
GRCh37.p13 chr 14	NC_000014.8:g.71232453_71232467dup
GRCh37.p13 chr 14	NC_000014.8:g.71232453_71232467A[24]CAAAAAAAAAAAAAAA[1]

Gene: MAP3K9, mitogen-activated protein kinase kinase kinase 9 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAP3K9 transcript variant 2	NM_001284230.2:c.821-4556… NM_001284230.2:c.821-4556_821-4554del	N/A	Intron Variant
MAP3K9 transcript variant 3	NM_001284231.1:c.-15-251_… NM_001284231.1:c.-15-251_-15-249del	N/A	Intron Variant
MAP3K9 transcript variant 4	NM_001284232.1:c.-98-4556… NM_001284232.1:c.-98-4556_-98-4554del	N/A	Intron Variant
MAP3K9 transcript variant 1	NM_033141.4:c.821-4556_82… NM_033141.4:c.821-4556_821-4554del	N/A	Intron Variant
MAP3K9 transcript variant X2	XM_005267683.6:c.821-4556… XM_005267683.6:c.821-4556_821-4554del	N/A	Intron Variant
MAP3K9 transcript variant X1	XM_011536788.4:c.821-4556… XM_011536788.4:c.821-4556_821-4554del	N/A	Intron Variant
MAP3K9 transcript variant X3	XM_011536792.1:c.-98-4556… XM_011536792.1:c.-98-4556_-98-4554del	N/A	Intron Variant
MAP3K9 transcript variant X4	XM_011536794.3:c.	N/A	Genic Upstream Transcript 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)₁₅=	delAAA	delAA	delA	dupA	dupAA	dup(A)₉	dup(A)₁₅	ins(A)₉C(A)₁₅
GRCh38.p14 chr 14	NC_000014.9:g.70765736_70765750=	NC_000014.9:g.70765748_70765750del	NC_000014.9:g.70765749_70765750del	NC_000014.9:g.70765750del	NC_000014.9:g.70765750dup	NC_000014.9:g.70765749_70765750dup	NC_000014.9:g.70765742_70765750dup	NC_000014.9:g.70765736_70765750dup	NC_000014.9:g.70765736_70765750A[24]CAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 14	NC_000014.8:g.71232453_71232467=	NC_000014.8:g.71232465_71232467del	NC_000014.8:g.71232466_71232467del	NC_000014.8:g.71232467del	NC_000014.8:g.71232467dup	NC_000014.8:g.71232466_71232467dup	NC_000014.8:g.71232459_71232467dup	NC_000014.8:g.71232453_71232467dup	NC_000014.8:g.71232453_71232467A[24]CAAAAAAAAAAAAAAA[1]
MAP3K9 transcript variant 2	NM_001284230.2:c.821-4554=	NM_001284230.2:c.821-4556_821-4554del	NM_001284230.2:c.821-4555_821-4554del	NM_001284230.2:c.821-4554del	NM_001284230.2:c.821-4554dup	NM_001284230.2:c.821-4555_821-4554dup	NM_001284230.2:c.821-4562_821-4554dup	NM_001284230.2:c.821-4568_821-4554dup	NM_001284230.2:c.821-4554_821-4553insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript variant 3	NM_001284231.1:c.-15-249=	NM_001284231.1:c.-15-251_-15-249del	NM_001284231.1:c.-15-250_-15-249del	NM_001284231.1:c.-15-249del	NM_001284231.1:c.-15-249dup	NM_001284231.1:c.-15-250_-15-249dup	NM_001284231.1:c.-15-257_-15-249dup	NM_001284231.1:c.-15-263_-15-249dup	NM_001284231.1:c.-15-249_-15-248insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript variant 4	NM_001284232.1:c.-98-4554=	NM_001284232.1:c.-98-4556_-98-4554del	NM_001284232.1:c.-98-4555_-98-4554del	NM_001284232.1:c.-98-4554del	NM_001284232.1:c.-98-4554dup	NM_001284232.1:c.-98-4555_-98-4554dup	NM_001284232.1:c.-98-4562_-98-4554dup	NM_001284232.1:c.-98-4568_-98-4554dup	NM_001284232.1:c.-98-4554_-98-4553insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript	NM_033141.2:c.821-4554=	NM_033141.2:c.821-4556_821-4554del	NM_033141.2:c.821-4555_821-4554del	NM_033141.2:c.821-4554del	NM_033141.2:c.821-4554dup	NM_033141.2:c.821-4555_821-4554dup	NM_033141.2:c.821-4562_821-4554dup	NM_033141.2:c.821-4568_821-4554dup	NM_033141.2:c.821-4554_821-4553insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript variant 1	NM_033141.4:c.821-4554=	NM_033141.4:c.821-4556_821-4554del	NM_033141.4:c.821-4555_821-4554del	NM_033141.4:c.821-4554del	NM_033141.4:c.821-4554dup	NM_033141.4:c.821-4555_821-4554dup	NM_033141.4:c.821-4562_821-4554dup	NM_033141.4:c.821-4568_821-4554dup	NM_033141.4:c.821-4554_821-4553insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript variant X1	XM_005267682.1:c.821-4554=	XM_005267682.1:c.821-4556_821-4554del	XM_005267682.1:c.821-4555_821-4554del	XM_005267682.1:c.821-4554del	XM_005267682.1:c.821-4554dup	XM_005267682.1:c.821-4555_821-4554dup	XM_005267682.1:c.821-4562_821-4554dup	XM_005267682.1:c.821-4568_821-4554dup	XM_005267682.1:c.821-4554_821-4553insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript variant X2	XM_005267683.1:c.821-4554=	XM_005267683.1:c.821-4556_821-4554del	XM_005267683.1:c.821-4555_821-4554del	XM_005267683.1:c.821-4554del	XM_005267683.1:c.821-4554dup	XM_005267683.1:c.821-4555_821-4554dup	XM_005267683.1:c.821-4562_821-4554dup	XM_005267683.1:c.821-4568_821-4554dup	XM_005267683.1:c.821-4554_821-4553insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript variant X2	XM_005267683.6:c.821-4554=	XM_005267683.6:c.821-4556_821-4554del	XM_005267683.6:c.821-4555_821-4554del	XM_005267683.6:c.821-4554del	XM_005267683.6:c.821-4554dup	XM_005267683.6:c.821-4555_821-4554dup	XM_005267683.6:c.821-4562_821-4554dup	XM_005267683.6:c.821-4568_821-4554dup	XM_005267683.6:c.821-4554_821-4553insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript variant X3	XM_005267684.1:c.-98-4554=	XM_005267684.1:c.-98-4556_-98-4554del	XM_005267684.1:c.-98-4555_-98-4554del	XM_005267684.1:c.-98-4554del	XM_005267684.1:c.-98-4554dup	XM_005267684.1:c.-98-4555_-98-4554dup	XM_005267684.1:c.-98-4562_-98-4554dup	XM_005267684.1:c.-98-4568_-98-4554dup	XM_005267684.1:c.-98-4554_-98-4553insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript variant X4	XM_005267685.1:c.-15-249=	XM_005267685.1:c.-15-251_-15-249del	XM_005267685.1:c.-15-250_-15-249del	XM_005267685.1:c.-15-249del	XM_005267685.1:c.-15-249dup	XM_005267685.1:c.-15-250_-15-249dup	XM_005267685.1:c.-15-257_-15-249dup	XM_005267685.1:c.-15-263_-15-249dup	XM_005267685.1:c.-15-249_-15-248insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript variant X1	XM_011536788.4:c.821-4554=	XM_011536788.4:c.821-4556_821-4554del	XM_011536788.4:c.821-4555_821-4554del	XM_011536788.4:c.821-4554del	XM_011536788.4:c.821-4554dup	XM_011536788.4:c.821-4555_821-4554dup	XM_011536788.4:c.821-4562_821-4554dup	XM_011536788.4:c.821-4568_821-4554dup	XM_011536788.4:c.821-4554_821-4553insTTTTTTTTTTTTTTTGTTTTTTTTT
MAP3K9 transcript variant X3	XM_011536792.1:c.-98-4554=	XM_011536792.1:c.-98-4556_-98-4554del	XM_011536792.1:c.-98-4555_-98-4554del	XM_011536792.1:c.-98-4554del	XM_011536792.1:c.-98-4554dup	XM_011536792.1:c.-98-4555_-98-4554dup	XM_011536792.1:c.-98-4562_-98-4554dup	XM_011536792.1:c.-98-4568_-98-4554dup	XM_011536792.1:c.-98-4554_-98-4553insTTTTTTTTTTTTTTTGTTTTTTTTT

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#.

40 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77932703	Apr 25, 2013 (138)
2	HGSV	ss77938512	Apr 25, 2013 (138)
3	HGSV	ss77944914	Apr 25, 2013 (138)
4	HGSV	ss80471983	Apr 25, 2013 (138)
5	HGSV	ss82159167	Apr 25, 2013 (138)
6	PJP	ss294837656	May 09, 2011 (137)
7	SSMP	ss664240665	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1710642334	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710642335	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710642346	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710642348	Apr 01, 2015 (144)
12	SYSTEMSBIOZJU	ss2628544110	Nov 08, 2017 (151)
13	SWEGEN	ss3012416620	Nov 08, 2017 (151)
14	EVA_DECODE	ss3696940035	Jul 13, 2019 (153)
15	EVA_DECODE	ss3696940036	Jul 13, 2019 (153)
16	EVA_DECODE	ss3696940037	Jul 13, 2019 (153)
17	ACPOP	ss3740498663	Jul 13, 2019 (153)
18	ACPOP	ss3740498664	Jul 13, 2019 (153)
19	PACBIO	ss3787702023	Jul 13, 2019 (153)
20	PACBIO	ss3792734428	Jul 13, 2019 (153)
21	PACBIO	ss3797618747	Jul 13, 2019 (153)
22	EVA	ss3833987133	Apr 27, 2020 (154)
23	GNOMAD	ss4280336439	Apr 27, 2021 (155)
24	GNOMAD	ss4280336440	Apr 27, 2021 (155)
25	GNOMAD	ss4280336441	Apr 27, 2021 (155)
26	GNOMAD	ss4280336442	Apr 27, 2021 (155)
27	GNOMAD	ss4280336443	Apr 27, 2021 (155)
28	GNOMAD	ss4280336447	Apr 27, 2021 (155)
29	GNOMAD	ss4280336448	Apr 27, 2021 (155)
30	GNOMAD	ss4280336449	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5213828974	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5213828975	Apr 27, 2021 (155)
33	TOMMO_GENOMICS	ss5213828976	Apr 27, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5296686408	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5490684617	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5490684618	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5766803981	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5766803982	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5766803983	Oct 16, 2022 (156)
40	EVA	ss5901873727	Oct 16, 2022 (156)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455011438 (NC_000014.9:70765735::A 5/112294) Row 455011439 (NC_000014.9:70765735::AA 1/112298) Row 455011440 (NC_000014.9:70765735::AAAAAAAAA 12/112282)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455011438 (NC_000014.9:70765735::A 5/112294) Row 455011439 (NC_000014.9:70765735::AA 1/112298) Row 455011440 (NC_000014.9:70765735::AAAAAAAAA 12/112282)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455011438 (NC_000014.9:70765735::A 5/112294) Row 455011439 (NC_000014.9:70765735::AA 1/112298) Row 455011440 (NC_000014.9:70765735::AAAAAAAAA 12/112282)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455011438 (NC_000014.9:70765735::A 5/112294) Row 455011439 (NC_000014.9:70765735::AA 1/112298) Row 455011440 (NC_000014.9:70765735::AAAAAAAAA 12/112282)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455011438 (NC_000014.9:70765735::A 5/112294) Row 455011439 (NC_000014.9:70765735::AA 1/112298) Row 455011440 (NC_000014.9:70765735::AAAAAAAAA 12/112282)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455011438 (NC_000014.9:70765735::A 5/112294) Row 455011439 (NC_000014.9:70765735::AA 1/112298) Row 455011440 (NC_000014.9:70765735::AAAAAAAAA 12/112282)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455011438 (NC_000014.9:70765735::A 5/112294) Row 455011439 (NC_000014.9:70765735::AA 1/112298) Row 455011440 (NC_000014.9:70765735::AAAAAAAAA 12/112282)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455011438 (NC_000014.9:70765735::A 5/112294) Row 455011439 (NC_000014.9:70765735::AA 1/112298) Row 455011440 (NC_000014.9:70765735::AAAAAAAAA 12/112282)...	-	Apr 27, 2021 (155)
49	Northern Sweden Submission ignored due to conflicting rows: Row 13783528 (NC_000014.8:71232452:AA: 171/550) Row 13783529 (NC_000014.8:71232452:A: 226/550)	-	Jul 13, 2019 (153)
50	Northern Sweden Submission ignored due to conflicting rows: Row 13783528 (NC_000014.8:71232452:AA: 171/550) Row 13783529 (NC_000014.8:71232452:A: 226/550)	-	Jul 13, 2019 (153)
51	8.3KJPN Submission ignored due to conflicting rows: Row 71798281 (NC_000014.8:71232452:AA: 5393/16592) Row 71798282 (NC_000014.8:71232452:A: 9893/16592) Row 71798283 (NC_000014.8:71232452:AAA: 7/16592)	-	Apr 27, 2021 (155)
52	8.3KJPN Submission ignored due to conflicting rows: Row 71798281 (NC_000014.8:71232452:AA: 5393/16592) Row 71798282 (NC_000014.8:71232452:A: 9893/16592) Row 71798283 (NC_000014.8:71232452:AAA: 7/16592)	-	Apr 27, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 71798281 (NC_000014.8:71232452:AA: 5393/16592) Row 71798282 (NC_000014.8:71232452:A: 9893/16592) Row 71798283 (NC_000014.8:71232452:AAA: 7/16592)	-	Apr 27, 2021 (155)
54	14KJPN Submission ignored due to conflicting rows: Row 100641085 (NC_000014.9:70765735:AA: 9383/27914) Row 100641086 (NC_000014.9:70765735:A: 16467/27914) Row 100641087 (NC_000014.9:70765735:AAA: 6/27914)	-	Oct 16, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 100641085 (NC_000014.9:70765735:AA: 9383/27914) Row 100641086 (NC_000014.9:70765735:A: 16467/27914) Row 100641087 (NC_000014.9:70765735:AAA: 6/27914)	-	Oct 16, 2022 (156)
56	14KJPN Submission ignored due to conflicting rows: Row 100641085 (NC_000014.9:70765735:AA: 9383/27914) Row 100641086 (NC_000014.9:70765735:A: 16467/27914) Row 100641087 (NC_000014.9:70765735:AAA: 6/27914)	-	Oct 16, 2022 (156)
57	ALFA	NC_000014.9 - 70765736	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)
rs36213611	Oct 25, 2006 (127)
rs71732634	May 11, 2012 (137)
rs143030217	May 04, 2012 (137)
rs370838896	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5213828976	NC_000014.8:71232452:AAA:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4280336449, ss5766803983	NC_000014.9:70765735:AAA:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
6710790459	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3012416620, ss3740498663, ss5213828974	NC_000014.8:71232452:AA:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1710642335, ss1710642348	NC_000014.8:71232465:AA:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4280336448, ss5490684618, ss5766803981	NC_000014.9:70765735:AA:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
6710790459	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3696940037	NC_000014.9:70765748:AA:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss294837656	NC_000014.7:70302205:A:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss77932703, ss77938512, ss77944914, ss80471983, ss82159167	NC_000014.7:70302219:A:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss664240665, ss2628544110, ss3740498664, ss3787702023, ss3792734428, ss3797618747, ss3833987133, ss5213828975	NC_000014.8:71232452:A:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1710642334, ss1710642346	NC_000014.8:71232466:A:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4280336447, ss5296686408, ss5490684617, ss5766803982, ss5901873727	NC_000014.9:70765735:A:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
6710790459	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3696940036	NC_000014.9:70765749:A:	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4280336439	NC_000014.9:70765735::A	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
6710790459	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4280336440	NC_000014.9:70765735::AA	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3696940035	NC_000014.9:70765750::AA	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4280336441	NC_000014.9:70765735::AAAAAAAAA	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4280336442	NC_000014.9:70765735::AAAAAAAAAAAA… NC_000014.9:70765735::AAAAAAAAAAAAAAA	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4280336443	NC_000014.9:70765735::AAAAAAAAAAAA… NC_000014.9:70765735::AAAAAAAAAAAAAAAAAAAAAAAAC	NC_000014.9:70765735:AAAAAAAAAAAAA… NC_000014.9:70765735:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAA	(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 rs10523480

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

rs10523480