Name: rs35015191
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.

rs35015191

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:151190666-151190685 (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(A)₁₂ / del(A)₁₀ / del(A)₇ / de…
del(A)₁₂ / del(A)₁₀ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / ins(A)₅T(A)₅₈
Variation Type: Indel Insertion and Deletion
Frequency: (A)₂₀=0.2911 (1458/5008, 1000G)
del(A)₁₂=0.000 (0/670, ALFA)
del(A)₁₀=0.000 (0/670, ALFA) (+ 8 more)
del(A)₇=0.000 (0/670, ALFA)
del(A)₅=0.000 (0/670, ALFA)
del(A)₄=0.000 (0/670, ALFA)
delAAA=0.000 (0/670, ALFA)
delAA=0.000 (0/670, ALFA)
delA=0.000 (0/670, ALFA)
dupA=0.000 (0/670, ALFA)
dupAA=0.000 (0/670, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CCDC69 : 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	670	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	566	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	42	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAAAAAA=0	AAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	42	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	26	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	24	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	4	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	12	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAAAA=0	AAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	20	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₂₀=0.2911	delAAA=0.7089
1000Genomes	African	Sub	1322	(A)₂₀=0.3343	delAAA=0.6657
1000Genomes	East Asian	Sub	1008	(A)₂₀=0.3968	delAAA=0.6032
1000Genomes	Europe	Sub	1006	(A)₂₀=0.2634	delAAA=0.7366
1000Genomes	South Asian	Sub	978	(A)₂₀=0.216	delAAA=0.784
1000Genomes	American	Sub	694	(A)₂₀=0.202	delAAA=0.798
Allele Frequency Aggregator	Total	Global	670	(A)₂₀=1.000	del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	European	Sub	566	(A)₂₀=1.000	del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	African	Sub	42	(A)₂₀=1.00	del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	26	(A)₂₀=1.00	del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Other	Sub	20	(A)₂₀=1.00	del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	12	(A)₂₀=1.00	del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	4	(A)₂₀=1.0	del(A)₁₂=0.0, del(A)₁₀=0.0, del(A)₇=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₂₀=0	del(A)₁₂=0, del(A)₁₀=0, del(A)₇=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=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 5	NC_000005.10:g.151190674_151190685del
GRCh38.p14 chr 5	NC_000005.10:g.151190676_151190685del
GRCh38.p14 chr 5	NC_000005.10:g.151190679_151190685del
GRCh38.p14 chr 5	NC_000005.10:g.151190680_151190685del
GRCh38.p14 chr 5	NC_000005.10:g.151190681_151190685del
GRCh38.p14 chr 5	NC_000005.10:g.151190682_151190685del
GRCh38.p14 chr 5	NC_000005.10:g.151190683_151190685del
GRCh38.p14 chr 5	NC_000005.10:g.151190684_151190685del
GRCh38.p14 chr 5	NC_000005.10:g.151190685del
GRCh38.p14 chr 5	NC_000005.10:g.151190685dup
GRCh38.p14 chr 5	NC_000005.10:g.151190684_151190685dup
GRCh38.p14 chr 5	NC_000005.10:g.151190683_151190685dup
GRCh38.p14 chr 5	NC_000005.10:g.151190666_151190685A[25]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 5	NC_000005.9:g.150570235_150570246del
GRCh37.p13 chr 5	NC_000005.9:g.150570237_150570246del
GRCh37.p13 chr 5	NC_000005.9:g.150570240_150570246del
GRCh37.p13 chr 5	NC_000005.9:g.150570241_150570246del
GRCh37.p13 chr 5	NC_000005.9:g.150570242_150570246del
GRCh37.p13 chr 5	NC_000005.9:g.150570243_150570246del
GRCh37.p13 chr 5	NC_000005.9:g.150570244_150570246del
GRCh37.p13 chr 5	NC_000005.9:g.150570245_150570246del
GRCh37.p13 chr 5	NC_000005.9:g.150570246del
GRCh37.p13 chr 5	NC_000005.9:g.150570246dup
GRCh37.p13 chr 5	NC_000005.9:g.150570245_150570246dup
GRCh37.p13 chr 5	NC_000005.9:g.150570244_150570246dup
GRCh37.p13 chr 5	NC_000005.9:g.150570227_150570246A[25]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

Gene: CCDC69, coiled-coil domain containing 69 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CCDC69 transcript	NM_015621.3:c.320-3218_32… NM_015621.3:c.320-3218_320-3207del	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)₂₀=	del(A)₁₂	del(A)₁₀	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	ins(A)₅T(A)₅₈
GRCh38.p14 chr 5	NC_000005.10:g.151190666_151190685=	NC_000005.10:g.151190674_151190685del	NC_000005.10:g.151190676_151190685del	NC_000005.10:g.151190679_151190685del	NC_000005.10:g.151190680_151190685del	NC_000005.10:g.151190681_151190685del	NC_000005.10:g.151190682_151190685del	NC_000005.10:g.151190683_151190685del	NC_000005.10:g.151190684_151190685del	NC_000005.10:g.151190685del	NC_000005.10:g.151190685dup	NC_000005.10:g.151190684_151190685dup	NC_000005.10:g.151190683_151190685dup	NC_000005.10:g.151190666_151190685A[25]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 5	NC_000005.9:g.150570227_150570246=	NC_000005.9:g.150570235_150570246del	NC_000005.9:g.150570237_150570246del	NC_000005.9:g.150570240_150570246del	NC_000005.9:g.150570241_150570246del	NC_000005.9:g.150570242_150570246del	NC_000005.9:g.150570243_150570246del	NC_000005.9:g.150570244_150570246del	NC_000005.9:g.150570245_150570246del	NC_000005.9:g.150570246del	NC_000005.9:g.150570246dup	NC_000005.9:g.150570245_150570246dup	NC_000005.9:g.150570244_150570246dup	NC_000005.9:g.150570227_150570246A[25]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC69 transcript	NM_015621.2:c.320-3207=	NM_015621.2:c.320-3218_320-3207del	NM_015621.2:c.320-3216_320-3207del	NM_015621.2:c.320-3213_320-3207del	NM_015621.2:c.320-3212_320-3207del	NM_015621.2:c.320-3211_320-3207del	NM_015621.2:c.320-3210_320-3207del	NM_015621.2:c.320-3209_320-3207del	NM_015621.2:c.320-3208_320-3207del	NM_015621.2:c.320-3207del	NM_015621.2:c.320-3207dup	NM_015621.2:c.320-3208_320-3207dup	NM_015621.2:c.320-3209_320-3207dup	NM_015621.2:c.320-3207_320-3206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTT
CCDC69 transcript	NM_015621.3:c.320-3207=	NM_015621.3:c.320-3218_320-3207del	NM_015621.3:c.320-3216_320-3207del	NM_015621.3:c.320-3213_320-3207del	NM_015621.3:c.320-3212_320-3207del	NM_015621.3:c.320-3211_320-3207del	NM_015621.3:c.320-3210_320-3207del	NM_015621.3:c.320-3209_320-3207del	NM_015621.3:c.320-3208_320-3207del	NM_015621.3:c.320-3207del	NM_015621.3:c.320-3207dup	NM_015621.3:c.320-3208_320-3207dup	NM_015621.3:c.320-3209_320-3207dup	NM_015621.3:c.320-3207_320-3206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTT

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#.

59 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42483450	Mar 15, 2016 (147)
2	ABI	ss42512832	Mar 15, 2006 (126)
3	HGSV	ss80387601	Dec 15, 2007 (135)
4	HUMANGENOME_JCVI	ss98684042	Mar 15, 2016 (147)
5	PJP	ss295250696	May 09, 2011 (134)
6	PJP	ss295250697	May 09, 2011 (137)
7	1000GENOMES	ss1374678402	Aug 21, 2014 (142)
8	EVA_UK10K_ALSPAC	ss1704920871	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1704921291	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710237257	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710237258	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710237259	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1710237260	Apr 01, 2015 (144)
14	SWEGEN	ss2998009104	Nov 08, 2017 (151)
15	MCHAISSO	ss3064179565	Nov 08, 2017 (151)
16	MCHAISSO	ss3065056055	Nov 08, 2017 (151)
17	MCHAISSO	ss3065056056	Nov 08, 2017 (151)
18	MCHAISSO	ss3066048868	Nov 08, 2017 (151)
19	EVA_DECODE	ss3715964384	Jul 13, 2019 (153)
20	EVA_DECODE	ss3715964385	Jul 13, 2019 (153)
21	EVA_DECODE	ss3715964386	Jul 13, 2019 (153)
22	EVA_DECODE	ss3715964387	Jul 13, 2019 (153)
23	EVA_DECODE	ss3715964388	Jul 13, 2019 (153)
24	EVA_DECODE	ss3715964389	Jul 13, 2019 (153)
25	PACBIO	ss3785284743	Jul 13, 2019 (153)
26	PACBIO	ss3790662014	Jul 13, 2019 (153)
27	PACBIO	ss3795539061	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3807397187	Jul 13, 2019 (153)
29	EVA	ss3829570013	Apr 26, 2020 (154)
30	GNOMAD	ss4131746879	Apr 26, 2021 (155)
31	GNOMAD	ss4131746880	Apr 26, 2021 (155)
32	GNOMAD	ss4131746881	Apr 26, 2021 (155)
33	GNOMAD	ss4131746883	Apr 26, 2021 (155)
34	GNOMAD	ss4131746884	Apr 26, 2021 (155)
35	GNOMAD	ss4131746885	Apr 26, 2021 (155)
36	GNOMAD	ss4131746886	Apr 26, 2021 (155)
37	GNOMAD	ss4131746887	Apr 26, 2021 (155)
38	GNOMAD	ss4131746888	Apr 26, 2021 (155)
39	GNOMAD	ss4131746889	Apr 26, 2021 (155)
40	GNOMAD	ss4131746890	Apr 26, 2021 (155)
41	GNOMAD	ss4131746891	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5174757937	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5174757938	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5174757939	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5174757940	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5174757941	Apr 26, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5266318443	Oct 13, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5266318444	Oct 13, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5266318445	Oct 13, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5266318446	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5464235470	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5464235471	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5464235472	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5464235473	Oct 13, 2022 (156)
55	TOMMO_GENOMICS	ss5712015705	Oct 13, 2022 (156)
56	TOMMO_GENOMICS	ss5712015706	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5712015708	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5712015709	Oct 13, 2022 (156)
59	EVA	ss5980323535	Oct 13, 2022 (156)
60	1000Genomes	NC_000005.9 - 150570227	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 16391932 (NC_000005.9:150570227:AA: 2417/3854) Row 16391934 (NC_000005.9:150570226:AAAA: 377/3854)	-	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 16391932 (NC_000005.9:150570227:AA: 2417/3854) Row 16391934 (NC_000005.9:150570226:AAAA: 377/3854)	-	Oct 12, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 208358204 (NC_000005.10:151190665::A 1067/85318) Row 208358205 (NC_000005.10:151190665::AA 11/85368) Row 208358206 (NC_000005.10:151190665::AAA 2/85368)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 32727244 (NC_000005.9:150570226:AA: 5415/16646) Row 32727245 (NC_000005.9:150570226:AAA: 2169/16646) Row 32727246 (NC_000005.9:150570226:AAAA: 117/16646)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 32727244 (NC_000005.9:150570226:AA: 5415/16646) Row 32727245 (NC_000005.9:150570226:AAA: 2169/16646) Row 32727246 (NC_000005.9:150570226:AAAA: 117/16646)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 32727244 (NC_000005.9:150570226:AA: 5415/16646) Row 32727245 (NC_000005.9:150570226:AAA: 2169/16646) Row 32727246 (NC_000005.9:150570226:AAAA: 117/16646)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 32727244 (NC_000005.9:150570226:AA: 5415/16646) Row 32727245 (NC_000005.9:150570226:AAA: 2169/16646) Row 32727246 (NC_000005.9:150570226:AAAA: 117/16646)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 32727244 (NC_000005.9:150570226:AA: 5415/16646) Row 32727245 (NC_000005.9:150570226:AAA: 2169/16646) Row 32727246 (NC_000005.9:150570226:AAAA: 117/16646)...	-	Apr 26, 2021 (155)
81	14KJPN Submission ignored due to conflicting rows: Row 45852809 (NC_000005.10:151190665:AA: 9546/27824) Row 45852810 (NC_000005.10:151190665:AAA: 3985/27824) Row 45852812 (NC_000005.10:151190665:AAAA: 205/27824)...	-	Oct 13, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 45852809 (NC_000005.10:151190665:AA: 9546/27824) Row 45852810 (NC_000005.10:151190665:AAA: 3985/27824) Row 45852812 (NC_000005.10:151190665:AAAA: 205/27824)...	-	Oct 13, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 45852809 (NC_000005.10:151190665:AA: 9546/27824) Row 45852810 (NC_000005.10:151190665:AAA: 3985/27824) Row 45852812 (NC_000005.10:151190665:AAAA: 205/27824)...	-	Oct 13, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 45852809 (NC_000005.10:151190665:AA: 9546/27824) Row 45852810 (NC_000005.10:151190665:AAA: 3985/27824) Row 45852812 (NC_000005.10:151190665:AAAA: 205/27824)...	-	Oct 13, 2022 (156)
85	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16391932 (NC_000005.9:150570227:AA: 2311/3708) Row 16391934 (NC_000005.9:150570226:AAAA: 360/3708)	-	Oct 12, 2018 (152)
86	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16391932 (NC_000005.9:150570227:AAA: 2311/3708) Row 16391933 (NC_000005.9:150570228:AA: 1026/3708) Row 16391934 (NC_000005.9:150570226:AAAA: 360/3708)	-	Apr 26, 2020 (154)
87	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16391932 (NC_000005.9:150570227:AA: 2311/3708) Row 16391934 (NC_000005.9:150570226:AAAA: 360/3708)	-	Oct 12, 2018 (152)
88	ALFA	NC_000005.10 - 151190666	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)
rs58326570	Oct 12, 2011 (135)
rs71589731	Oct 12, 2011 (135)
rs145466726	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3785284743, ss3790662014, ss3795539061	NC_000005.9:150570226:AAAAAAAAAAAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4131746891	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
8147693753	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4131746890	NC_000005.10:151190665:AAAAAAAAAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
8147693753	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4131746889	NC_000005.10:151190665:AAAAAAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
8147693753	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4131746888	NC_000005.10:151190665:AAAAAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3715964389, ss4131746887	NC_000005.10:151190665:AAAAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
8147693753	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss1704920871, ss1704921291, ss2998009104, ss5174757939	NC_000005.9:150570226:AAAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4131746886, ss5464235473, ss5712015708	NC_000005.10:151190665:AAAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
8147693753	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3715964388	NC_000005.10:151190666:AAAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss80387601	NC_000005.8:150550436:AAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
29458507, ss1374678402, ss5174757938	NC_000005.9:150570226:AAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1710237257, ss1710237258	NC_000005.9:150570227:AAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3065056055, ss3807397187, ss4131746885, ss5266318446, ss5464235470, ss5712015706	NC_000005.10:151190665:AAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
8147693753	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3715964387	NC_000005.10:151190667:AAA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss295250696	NC_000005.8:150550419:AA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss295250697	NC_000005.8:150550437:AA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3829570013, ss5174757937, ss5980323535	NC_000005.9:150570226:AA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
	NC_000005.9:150570227:AA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss1710237259, ss1710237260	NC_000005.9:150570228:AA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3064179565, ss3065056056, ss3066048868, ss4131746884, ss5266318443, ss5464235471, ss5712015705	NC_000005.10:151190665:AA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8147693753	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3715964386	NC_000005.10:151190668:AA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss98684042	NT_029289.11:11733171:AA:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5174757941	NC_000005.9:150570226:A:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4131746883, ss5266318444, ss5464235472, ss5712015709	NC_000005.10:151190665:A:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
8147693753	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3715964385	NC_000005.10:151190669:A:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss42512832	NT_029289.11:11733171:A:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss42483450	NT_029289.11:11733172:A:	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5174757940	NC_000005.9:150570226::A	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4131746879, ss5266318445	NC_000005.10:151190665::A	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
8147693753	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3715964384	NC_000005.10:151190670::A	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4131746880	NC_000005.10:151190665::AA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
8147693753	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131746881	NC_000005.10:151190665::AAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
	NC_000005.10:151190665::AAAAAAAAAA… NC_000005.10:151190665::AAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:151190665:AAAAAAAAAAA… NC_000005.10:151190665:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs35015191

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

rs35015191