Name: rs35145386
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.

rs35145386

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:61105630-61105644 (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)₅ / del(A)₄ / delAAA / delAA…
del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / ins(A)₂₀ / ins(A)₂₁ / ins(A)₉T(A)₆TGAACTGAAG(T)₄ATGTTTAAACATG(AATAAA)₂AAAAAATGAAACTG(A)₁₈
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₅=0.0000 (0/1900, ALFA)
del(A)₄=0.0000 (0/1900, ALFA)
delAAA=0.0000 (0/1900, ALFA) (+ 5 more)
delAA=0.0000 (0/1900, ALFA)
delA=0.0000 (0/1900, ALFA)
dupA=0.0000 (0/1900, ALFA)
dupAA=0.0000 (0/1900, ALFA)
(A)₁₅=0.45 (18/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NDUFAF2 : 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	1900	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	1000	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	740	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	38	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	702	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	30	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	52	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	16	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	60	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=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
Allele Frequency Aggregator	Total	Global	1900	(A)₁₅=1.0000	del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	1000	(A)₁₅=1.000	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	740	(A)₁₅=1.000	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	Other	Sub	60	(A)₁₅=1.00	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	52	(A)₁₅=1.00	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	30	(A)₁₅=1.00	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	South Asian	Sub	16	(A)₁₅=1.00	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	2	(A)₁₅=1.0	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
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₅=0.45	delA=0.55

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.61105640_61105644del
GRCh38.p14 chr 5	NC_000005.10:g.61105641_61105644del
GRCh38.p14 chr 5	NC_000005.10:g.61105642_61105644del
GRCh38.p14 chr 5	NC_000005.10:g.61105643_61105644del
GRCh38.p14 chr 5	NC_000005.10:g.61105644del
GRCh38.p14 chr 5	NC_000005.10:g.61105644dup
GRCh38.p14 chr 5	NC_000005.10:g.61105643_61105644dup
GRCh38.p14 chr 5	NC_000005.10:g.61105644_61105645insAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 5	NC_000005.10:g.61105644_61105645insAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 5	NC_000005.10:g.61105630_61105644A[24]TAAAAAATGAACTGAAGTTTTATGTTTAAACATGAATAAAAATAAAAAAAAATGAAACTGAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 5	NC_000005.9:g.60401467_60401471del
GRCh37.p13 chr 5	NC_000005.9:g.60401468_60401471del
GRCh37.p13 chr 5	NC_000005.9:g.60401469_60401471del
GRCh37.p13 chr 5	NC_000005.9:g.60401470_60401471del
GRCh37.p13 chr 5	NC_000005.9:g.60401471del
GRCh37.p13 chr 5	NC_000005.9:g.60401471dup
GRCh37.p13 chr 5	NC_000005.9:g.60401470_60401471dup
GRCh37.p13 chr 5	NC_000005.9:g.60401471_60401472insAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 5	NC_000005.9:g.60401471_60401472insAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 5	NC_000005.9:g.60401457_60401471A[24]TAAAAAATGAACTGAAGTTTTATGTTTAAACATGAATAAAAATAAAAAAAAATGAAACTGAAAAAAAAAAAAAAAAAA[1]
NDUFAF2 RefSeqGene	NG_008978.1:g.165512_165516del
NDUFAF2 RefSeqGene	NG_008978.1:g.165513_165516del
NDUFAF2 RefSeqGene	NG_008978.1:g.165514_165516del
NDUFAF2 RefSeqGene	NG_008978.1:g.165515_165516del
NDUFAF2 RefSeqGene	NG_008978.1:g.165516del
NDUFAF2 RefSeqGene	NG_008978.1:g.165516dup
NDUFAF2 RefSeqGene	NG_008978.1:g.165515_165516dup
NDUFAF2 RefSeqGene	NG_008978.1:g.165516_165517insAAAAAAAAAAAAAAAAAAAA
NDUFAF2 RefSeqGene	NG_008978.1:g.165516_165517insAAAAAAAAAAAAAAAAAAAAA
NDUFAF2 RefSeqGene	NG_008978.1:g.165502_165516A[24]TAAAAAATGAACTGAAGTTTTATGTTTAAACATGAATAAAAATAAAAAAAAATGAAACTGAAAAAAAAAAAAAAAAAA[1]

Gene: NDUFAF2, NADH:ubiquinone oxidoreductase complex assembly factor 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NDUFAF2 transcript	NM_174889.5:c.258+6608_25… NM_174889.5:c.258+6608_258+6612del	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)₁₅=	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	ins(A)₂₀	ins(A)₂₁	ins(A)₉T(A)₆TGAACTGAAG(T)₄ATGTTTAAACATG(AATAAA)₂AAAAAATGAAACTG(A)₁₈
GRCh38.p14 chr 5	NC_000005.10:g.61105630_61105644=	NC_000005.10:g.61105640_61105644del	NC_000005.10:g.61105641_61105644del	NC_000005.10:g.61105642_61105644del	NC_000005.10:g.61105643_61105644del	NC_000005.10:g.61105644del	NC_000005.10:g.61105644dup	NC_000005.10:g.61105643_61105644dup	NC_000005.10:g.61105644_61105645insAAAAAAAAAAAAAAAAAAAA	NC_000005.10:g.61105644_61105645insAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:g.61105630_61105644A[24]TAAAAAATGAACTGAAGTTTTATGTTTAAACATGAATAAAAATAAAAAAAAATGAAACTGAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 5	NC_000005.9:g.60401457_60401471=	NC_000005.9:g.60401467_60401471del	NC_000005.9:g.60401468_60401471del	NC_000005.9:g.60401469_60401471del	NC_000005.9:g.60401470_60401471del	NC_000005.9:g.60401471del	NC_000005.9:g.60401471dup	NC_000005.9:g.60401470_60401471dup	NC_000005.9:g.60401471_60401472insAAAAAAAAAAAAAAAAAAAA	NC_000005.9:g.60401471_60401472insAAAAAAAAAAAAAAAAAAAAA	NC_000005.9:g.60401457_60401471A[24]TAAAAAATGAACTGAAGTTTTATGTTTAAACATGAATAAAAATAAAAAAAAATGAAACTGAAAAAAAAAAAAAAAAAA[1]
NDUFAF2 RefSeqGene	NG_008978.1:g.165502_165516=	NG_008978.1:g.165512_165516del	NG_008978.1:g.165513_165516del	NG_008978.1:g.165514_165516del	NG_008978.1:g.165515_165516del	NG_008978.1:g.165516del	NG_008978.1:g.165516dup	NG_008978.1:g.165515_165516dup	NG_008978.1:g.165516_165517insAAAAAAAAAAAAAAAAAAAA	NG_008978.1:g.165516_165517insAAAAAAAAAAAAAAAAAAAAA	NG_008978.1:g.165502_165516A[24]TAAAAAATGAACTGAAGTTTTATGTTTAAACATGAATAAAAATAAAAAAAAATGAAACTGAAAAAAAAAAAAAAAAAA[1]
NDUFAF2 transcript	NM_174889.4:c.258+6598=	NM_174889.4:c.258+6608_258+6612del	NM_174889.4:c.258+6609_258+6612del	NM_174889.4:c.258+6610_258+6612del	NM_174889.4:c.258+6611_258+6612del	NM_174889.4:c.258+6612del	NM_174889.4:c.258+6612dup	NM_174889.4:c.258+6611_258+6612dup	NM_174889.4:c.258+6612_258+6613insAAAAAAAAAAAAAAAAAAAA	NM_174889.4:c.258+6612_258+6613insAAAAAAAAAAAAAAAAAAAAA	NM_174889.4:c.258+6612_258+6613insAAAAAAAAATAAAAAATGAACTGAAGTTTTATGTTTAAACATGAATAAAAATAAAAAAAAATGAAACTGAAAAAAAAAAAAAAAAAA
NDUFAF2 transcript	NM_174889.5:c.258+6598=	NM_174889.5:c.258+6608_258+6612del	NM_174889.5:c.258+6609_258+6612del	NM_174889.5:c.258+6610_258+6612del	NM_174889.5:c.258+6611_258+6612del	NM_174889.5:c.258+6612del	NM_174889.5:c.258+6612dup	NM_174889.5:c.258+6611_258+6612dup	NM_174889.5:c.258+6612_258+6613insAAAAAAAAAAAAAAAAAAAA	NM_174889.5:c.258+6612_258+6613insAAAAAAAAAAAAAAAAAAAAA	NM_174889.5:c.258+6612_258+6613insAAAAAAAAATAAAAAATGAACTGAAGTTTTATGTTTAAACATGAATAAAAATAAAAAAAAATGAAACTGAAAAAAAAAAAAAAAAAA

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#.

46 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42462791	Mar 14, 2006 (126)
2	HGSV	ss77920557	Sep 08, 2015 (146)
3	HGSV	ss77952410	Sep 08, 2015 (146)
4	HGSV	ss83831659	Sep 08, 2015 (146)
5	HUMANGENOME_JCVI	ss98676983	Feb 13, 2009 (137)
6	GMI	ss287773499	May 09, 2011 (137)
7	GMI	ss288633054	May 04, 2012 (137)
8	PJP	ss295226942	May 09, 2011 (137)
9	PJP	ss295226943	May 09, 2011 (134)
10	SSMP	ss663613103	Apr 01, 2015 (144)
11	BILGI_BIOE	ss666311830	Apr 25, 2013 (138)
12	EVA_GENOME_DK	ss1576521576	Apr 01, 2015 (144)
13	HAMMER_LAB	ss1803575675	Sep 08, 2015 (146)
14	SWEGEN	ss2997003073	Nov 08, 2017 (151)
15	MCHAISSO	ss3064158630	Nov 08, 2017 (151)
16	MCHAISSO	ss3065031585	Nov 08, 2017 (151)
17	URBANLAB	ss3648070706	Oct 12, 2018 (152)
18	EVA_DECODE	ss3714768829	Jul 13, 2019 (153)
19	EVA_DECODE	ss3714768830	Jul 13, 2019 (153)
20	EVA_DECODE	ss3714768831	Jul 13, 2019 (153)
21	EVA_DECODE	ss3714768832	Jul 13, 2019 (153)
22	PACBIO	ss3785122019	Jul 13, 2019 (153)
23	PACBIO	ss3790526769	Jul 13, 2019 (153)
24	PACBIO	ss3795403414	Jul 13, 2019 (153)
25	EVA	ss3829266467	Apr 26, 2020 (154)
26	EVA	ss3843545977	Apr 26, 2020 (154)
27	GNOMAD	ss4105214383	Apr 26, 2021 (155)
28	GNOMAD	ss4105214384	Apr 26, 2021 (155)
29	GNOMAD	ss4105214385	Apr 26, 2021 (155)
30	GNOMAD	ss4105214386	Apr 26, 2021 (155)
31	GNOMAD	ss4105214387	Apr 26, 2021 (155)
32	GNOMAD	ss4105214388	Apr 26, 2021 (155)
33	GNOMAD	ss4105214389	Apr 26, 2021 (155)
34	GNOMAD	ss4105214390	Apr 26, 2021 (155)
35	GNOMAD	ss4105214391	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5171933053	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5171933054	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5264124292	Oct 13, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5264124293	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5264124294	Oct 13, 2022 (156)
41	HUGCELL_USP	ss5462289873	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5462289874	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5462289875	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5708384002	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5708384003	Oct 13, 2022 (156)
46	EVA	ss5854830816	Oct 13, 2022 (156)
47	The Danish reference pan genome	NC_000005.9 - 60401457	Apr 26, 2020 (154)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189911200 (NC_000005.10:61105629::A 721/107722) Row 189911201 (NC_000005.10:61105629::AA 3/107784) Row 189911202 (NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA 1/107788)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189911200 (NC_000005.10:61105629::A 721/107722) Row 189911201 (NC_000005.10:61105629::AA 3/107784) Row 189911202 (NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA 1/107788)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189911200 (NC_000005.10:61105629::A 721/107722) Row 189911201 (NC_000005.10:61105629::AA 3/107784) Row 189911202 (NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA 1/107788)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189911200 (NC_000005.10:61105629::A 721/107722) Row 189911201 (NC_000005.10:61105629::AA 3/107784) Row 189911202 (NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA 1/107788)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189911200 (NC_000005.10:61105629::A 721/107722) Row 189911201 (NC_000005.10:61105629::AA 3/107784) Row 189911202 (NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA 1/107788)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189911200 (NC_000005.10:61105629::A 721/107722) Row 189911201 (NC_000005.10:61105629::AA 3/107784) Row 189911202 (NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA 1/107788)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189911200 (NC_000005.10:61105629::A 721/107722) Row 189911201 (NC_000005.10:61105629::AA 3/107784) Row 189911202 (NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA 1/107788)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189911200 (NC_000005.10:61105629::A 721/107722) Row 189911201 (NC_000005.10:61105629::AA 3/107784) Row 189911202 (NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA 1/107788)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189911200 (NC_000005.10:61105629::A 721/107722) Row 189911201 (NC_000005.10:61105629::AA 3/107784) Row 189911202 (NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA 1/107788)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189911200 (NC_000005.10:61105629::A 721/107722) Row 189911201 (NC_000005.10:61105629::AA 3/107784) Row 189911202 (NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA 1/107788)...	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 29902360 (NC_000005.9:60401456:A: 15187/16758) Row 29902361 (NC_000005.9:60401456:AA: 197/16758)	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 29902360 (NC_000005.9:60401456:A: 15187/16758) Row 29902361 (NC_000005.9:60401456:AA: 197/16758)	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 42221106 (NC_000005.10:61105629:A: 25886/28258) Row 42221107 (NC_000005.10:61105629:AA: 329/28258)	-	Oct 13, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 42221106 (NC_000005.10:61105629:A: 25886/28258) Row 42221107 (NC_000005.10:61105629:AA: 329/28258)	-	Oct 13, 2022 (156)
62	ALFA	NC_000005.10 - 61105630	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)
rs57301980	May 23, 2008 (130)
rs71606665	May 11, 2012 (137)
rs376207346	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4105214391	NC_000005.10:61105629:AAAAA:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
8306551755	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4105214390	NC_000005.10:61105629:AAAA:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
8306551755	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3714768832, ss4105214389	NC_000005.10:61105629:AAA:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
8306551755	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss2997003073, ss5171933054	NC_000005.9:60401456:AA:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4105214388, ss5264124293, ss5462289875, ss5708384003	NC_000005.10:61105629:AA:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
8306551755	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3714768831	NC_000005.10:61105630:AA:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss288633054, ss295226942	NC_000005.8:60437213:A:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss77920557, ss77952410, ss83831659, ss295226943	NC_000005.8:60437227:A:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
998393, ss663613103, ss666311830, ss1576521576, ss1803575675, ss3785122019, ss3790526769, ss3795403414, ss3829266467, ss5171933053	NC_000005.9:60401456:A:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3064158630, ss3065031585, ss3648070706, ss3843545977, ss4105214387, ss5264124292, ss5462289873, ss5708384002, ss5854830816	NC_000005.10:61105629:A:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
8306551755	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3714768830	NC_000005.10:61105631:A:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss98676983, ss287773499	NT_006713.15:10995815:A:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss42462791	NT_006713.15:10995829:A:	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4105214383, ss5264124294, ss5462289874	NC_000005.10:61105629::A	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
8306551755	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3714768829	NC_000005.10:61105632::A	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4105214384	NC_000005.10:61105629::AA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
8306551755	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4105214385	NC_000005.10:61105629::AAAAAAAAAAA… NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4105214386	NC_000005.10:61105629::AAAAAAAAAAA… NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAAA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
	NC_000005.10:61105629::AAAAAAAAAAA… NC_000005.10:61105629::AAAAAAAAAAAAAAAAAAAAAAAATAAAAAATGAACTGAAGTTTTATGTTTAAACATGAATAAAAATAAAAAAAAATGAAACTGAAA	NC_000005.10:61105629:AAAAAAAAAAAA… NC_000005.10:61105629:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAATAAAAAATGAACTGAAGTTTTATGTTTAAACATGAATAAAAATAAAAAAAAATGAAACTGAAAAAAAAAAAAAAAAAA	(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 rs35145386

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

rs35145386