Name: rs35349842
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.

rs35349842

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:72138913-72138928 (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)₄ / delAA / delA / dupA / du…
del(A)₄ / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₉
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.4197 (2102/5008, 1000G)
del(A)₄=0.0000 (0/4842, ALFA)
delAA=0.0000 (0/4842, ALFA) (+ 6 more)
delA=0.0000 (0/4842, ALFA)
dupA=0.0000 (0/4842, ALFA)
dupAA=0.0000 (0/4842, ALFA)
dupAAA=0.0000 (0/4842, ALFA)
dup(A)₄=0.0000 (0/4842, ALFA)
dup(A)₅=0.0000 (0/4842, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PMFBP1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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	- No frequency provided	dupA=0.4197
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.6112
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.3165
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.3290
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.451
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.293
Allele Frequency Aggregator	Total	Global	4842	(A)₁₆=1.0000	del(A)₄=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	3874	(A)₁₆=1.0000	del(A)₄=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	Latin American 2	Sub	366	(A)₁₆=1.000	del(A)₄=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	African	Sub	268	(A)₁₆=1.000	del(A)₄=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	172	(A)₁₆=1.000	del(A)₄=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 1	Sub	70	(A)₁₆=1.00	del(A)₄=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	Asian	Sub	52	(A)₁₆=1.00	del(A)₄=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	40	(A)₁₆=1.00	del(A)₄=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 16	NC_000016.10:g.72138925_72138928del
GRCh38.p14 chr 16	NC_000016.10:g.72138927_72138928del
GRCh38.p14 chr 16	NC_000016.10:g.72138928del
GRCh38.p14 chr 16	NC_000016.10:g.72138928dup
GRCh38.p14 chr 16	NC_000016.10:g.72138927_72138928dup
GRCh38.p14 chr 16	NC_000016.10:g.72138926_72138928dup
GRCh38.p14 chr 16	NC_000016.10:g.72138925_72138928dup
GRCh38.p14 chr 16	NC_000016.10:g.72138924_72138928dup
GRCh38.p14 chr 16	NC_000016.10:g.72138923_72138928dup
GRCh38.p14 chr 16	NC_000016.10:g.72138922_72138928dup
GRCh38.p14 chr 16	NC_000016.10:g.72138920_72138928dup
GRCh37.p13 chr 16	NC_000016.9:g.72172824_72172827del
GRCh37.p13 chr 16	NC_000016.9:g.72172826_72172827del
GRCh37.p13 chr 16	NC_000016.9:g.72172827del
GRCh37.p13 chr 16	NC_000016.9:g.72172827dup
GRCh37.p13 chr 16	NC_000016.9:g.72172826_72172827dup
GRCh37.p13 chr 16	NC_000016.9:g.72172825_72172827dup
GRCh37.p13 chr 16	NC_000016.9:g.72172824_72172827dup
GRCh37.p13 chr 16	NC_000016.9:g.72172823_72172827dup
GRCh37.p13 chr 16	NC_000016.9:g.72172822_72172827dup
GRCh37.p13 chr 16	NC_000016.9:g.72172821_72172827dup
GRCh37.p13 chr 16	NC_000016.9:g.72172819_72172827dup

Gene: PMFBP1, polyamine modulated factor 1 binding protein 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PMFBP1 transcript variant 2	NM_001160213.2:c.483+373_… NM_001160213.2:c.483+373_483+376del	N/A	Intron Variant
PMFBP1 transcript variant 1	NM_031293.3:c.918+373_918… NM_031293.3:c.918+373_918+376del	N/A	Intron Variant
PMFBP1 transcript variant X1	XM_011523357.4:c.918+373_… XM_011523357.4:c.918+373_918+376del	N/A	Intron Variant
PMFBP1 transcript variant X2	XM_011523358.4:c.918+373_… XM_011523358.4:c.918+373_918+376del	N/A	Intron Variant
PMFBP1 transcript variant X3	XM_011523360.4:c.918+373_… XM_011523360.4:c.918+373_918+376del	N/A	Intron Variant
PMFBP1 transcript variant X4	XM_011523361.4:c.918+373_… XM_011523361.4:c.918+373_918+376del	N/A	Intron Variant
PMFBP1 transcript variant X5	XM_011523362.4:c.909+373_… XM_011523362.4:c.909+373_909+376del	N/A	Intron Variant
PMFBP1 transcript variant X6	XM_047434734.1:c.918+373_… XM_047434734.1:c.918+373_918+376del	N/A	Intron Variant
PMFBP1 transcript variant X7	XM_047434735.1:c.228+373_… XM_047434735.1:c.228+373_228+376del	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)₁₆=	del(A)₄	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₉
GRCh38.p14 chr 16	NC_000016.10:g.72138913_72138928=	NC_000016.10:g.72138925_72138928del	NC_000016.10:g.72138927_72138928del	NC_000016.10:g.72138928del	NC_000016.10:g.72138928dup	NC_000016.10:g.72138927_72138928dup	NC_000016.10:g.72138926_72138928dup	NC_000016.10:g.72138925_72138928dup	NC_000016.10:g.72138924_72138928dup	NC_000016.10:g.72138923_72138928dup	NC_000016.10:g.72138922_72138928dup	NC_000016.10:g.72138920_72138928dup
GRCh37.p13 chr 16	NC_000016.9:g.72172812_72172827=	NC_000016.9:g.72172824_72172827del	NC_000016.9:g.72172826_72172827del	NC_000016.9:g.72172827del	NC_000016.9:g.72172827dup	NC_000016.9:g.72172826_72172827dup	NC_000016.9:g.72172825_72172827dup	NC_000016.9:g.72172824_72172827dup	NC_000016.9:g.72172823_72172827dup	NC_000016.9:g.72172822_72172827dup	NC_000016.9:g.72172821_72172827dup	NC_000016.9:g.72172819_72172827dup
PMFBP1 transcript variant 2	NM_001160213.1:c.483+376=	NM_001160213.1:c.483+373_483+376del	NM_001160213.1:c.483+375_483+376del	NM_001160213.1:c.483+376del	NM_001160213.1:c.483+376dup	NM_001160213.1:c.483+375_483+376dup	NM_001160213.1:c.483+374_483+376dup	NM_001160213.1:c.483+373_483+376dup	NM_001160213.1:c.483+372_483+376dup	NM_001160213.1:c.483+371_483+376dup	NM_001160213.1:c.483+370_483+376dup	NM_001160213.1:c.483+368_483+376dup
PMFBP1 transcript variant 2	NM_001160213.2:c.483+376=	NM_001160213.2:c.483+373_483+376del	NM_001160213.2:c.483+375_483+376del	NM_001160213.2:c.483+376del	NM_001160213.2:c.483+376dup	NM_001160213.2:c.483+375_483+376dup	NM_001160213.2:c.483+374_483+376dup	NM_001160213.2:c.483+373_483+376dup	NM_001160213.2:c.483+372_483+376dup	NM_001160213.2:c.483+371_483+376dup	NM_001160213.2:c.483+370_483+376dup	NM_001160213.2:c.483+368_483+376dup
PMFBP1 transcript variant 1	NM_031293.2:c.918+376=	NM_031293.2:c.918+373_918+376del	NM_031293.2:c.918+375_918+376del	NM_031293.2:c.918+376del	NM_031293.2:c.918+376dup	NM_031293.2:c.918+375_918+376dup	NM_031293.2:c.918+374_918+376dup	NM_031293.2:c.918+373_918+376dup	NM_031293.2:c.918+372_918+376dup	NM_031293.2:c.918+371_918+376dup	NM_031293.2:c.918+370_918+376dup	NM_031293.2:c.918+368_918+376dup
PMFBP1 transcript variant 1	NM_031293.3:c.918+376=	NM_031293.3:c.918+373_918+376del	NM_031293.3:c.918+375_918+376del	NM_031293.3:c.918+376del	NM_031293.3:c.918+376dup	NM_031293.3:c.918+375_918+376dup	NM_031293.3:c.918+374_918+376dup	NM_031293.3:c.918+373_918+376dup	NM_031293.3:c.918+372_918+376dup	NM_031293.3:c.918+371_918+376dup	NM_031293.3:c.918+370_918+376dup	NM_031293.3:c.918+368_918+376dup
PMFBP1 transcript variant X1	XM_005256186.1:c.918+376=	XM_005256186.1:c.918+373_918+376del	XM_005256186.1:c.918+375_918+376del	XM_005256186.1:c.918+376del	XM_005256186.1:c.918+376dup	XM_005256186.1:c.918+375_918+376dup	XM_005256186.1:c.918+374_918+376dup	XM_005256186.1:c.918+373_918+376dup	XM_005256186.1:c.918+372_918+376dup	XM_005256186.1:c.918+371_918+376dup	XM_005256186.1:c.918+370_918+376dup	XM_005256186.1:c.918+368_918+376dup
PMFBP1 transcript variant X2	XM_005256187.1:c.918+376=	XM_005256187.1:c.918+373_918+376del	XM_005256187.1:c.918+375_918+376del	XM_005256187.1:c.918+376del	XM_005256187.1:c.918+376dup	XM_005256187.1:c.918+375_918+376dup	XM_005256187.1:c.918+374_918+376dup	XM_005256187.1:c.918+373_918+376dup	XM_005256187.1:c.918+372_918+376dup	XM_005256187.1:c.918+371_918+376dup	XM_005256187.1:c.918+370_918+376dup	XM_005256187.1:c.918+368_918+376dup
PMFBP1 transcript variant X1	XM_011523357.4:c.918+376=	XM_011523357.4:c.918+373_918+376del	XM_011523357.4:c.918+375_918+376del	XM_011523357.4:c.918+376del	XM_011523357.4:c.918+376dup	XM_011523357.4:c.918+375_918+376dup	XM_011523357.4:c.918+374_918+376dup	XM_011523357.4:c.918+373_918+376dup	XM_011523357.4:c.918+372_918+376dup	XM_011523357.4:c.918+371_918+376dup	XM_011523357.4:c.918+370_918+376dup	XM_011523357.4:c.918+368_918+376dup
PMFBP1 transcript variant X2	XM_011523358.4:c.918+376=	XM_011523358.4:c.918+373_918+376del	XM_011523358.4:c.918+375_918+376del	XM_011523358.4:c.918+376del	XM_011523358.4:c.918+376dup	XM_011523358.4:c.918+375_918+376dup	XM_011523358.4:c.918+374_918+376dup	XM_011523358.4:c.918+373_918+376dup	XM_011523358.4:c.918+372_918+376dup	XM_011523358.4:c.918+371_918+376dup	XM_011523358.4:c.918+370_918+376dup	XM_011523358.4:c.918+368_918+376dup
PMFBP1 transcript variant X3	XM_011523360.4:c.918+376=	XM_011523360.4:c.918+373_918+376del	XM_011523360.4:c.918+375_918+376del	XM_011523360.4:c.918+376del	XM_011523360.4:c.918+376dup	XM_011523360.4:c.918+375_918+376dup	XM_011523360.4:c.918+374_918+376dup	XM_011523360.4:c.918+373_918+376dup	XM_011523360.4:c.918+372_918+376dup	XM_011523360.4:c.918+371_918+376dup	XM_011523360.4:c.918+370_918+376dup	XM_011523360.4:c.918+368_918+376dup
PMFBP1 transcript variant X4	XM_011523361.4:c.918+376=	XM_011523361.4:c.918+373_918+376del	XM_011523361.4:c.918+375_918+376del	XM_011523361.4:c.918+376del	XM_011523361.4:c.918+376dup	XM_011523361.4:c.918+375_918+376dup	XM_011523361.4:c.918+374_918+376dup	XM_011523361.4:c.918+373_918+376dup	XM_011523361.4:c.918+372_918+376dup	XM_011523361.4:c.918+371_918+376dup	XM_011523361.4:c.918+370_918+376dup	XM_011523361.4:c.918+368_918+376dup
PMFBP1 transcript variant X5	XM_011523362.4:c.909+376=	XM_011523362.4:c.909+373_909+376del	XM_011523362.4:c.909+375_909+376del	XM_011523362.4:c.909+376del	XM_011523362.4:c.909+376dup	XM_011523362.4:c.909+375_909+376dup	XM_011523362.4:c.909+374_909+376dup	XM_011523362.4:c.909+373_909+376dup	XM_011523362.4:c.909+372_909+376dup	XM_011523362.4:c.909+371_909+376dup	XM_011523362.4:c.909+370_909+376dup	XM_011523362.4:c.909+368_909+376dup
PMFBP1 transcript variant X6	XM_047434734.1:c.918+376=	XM_047434734.1:c.918+373_918+376del	XM_047434734.1:c.918+375_918+376del	XM_047434734.1:c.918+376del	XM_047434734.1:c.918+376dup	XM_047434734.1:c.918+375_918+376dup	XM_047434734.1:c.918+374_918+376dup	XM_047434734.1:c.918+373_918+376dup	XM_047434734.1:c.918+372_918+376dup	XM_047434734.1:c.918+371_918+376dup	XM_047434734.1:c.918+370_918+376dup	XM_047434734.1:c.918+368_918+376dup
PMFBP1 transcript variant X7	XM_047434735.1:c.228+376=	XM_047434735.1:c.228+373_228+376del	XM_047434735.1:c.228+375_228+376del	XM_047434735.1:c.228+376del	XM_047434735.1:c.228+376dup	XM_047434735.1:c.228+375_228+376dup	XM_047434735.1:c.228+374_228+376dup	XM_047434735.1:c.228+373_228+376dup	XM_047434735.1:c.228+372_228+376dup	XM_047434735.1:c.228+371_228+376dup	XM_047434735.1:c.228+370_228+376dup	XM_047434735.1:c.228+368_228+376dup

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#.

49 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40677876	Oct 12, 2018 (152)
2	HGSV	ss81133557	Oct 12, 2018 (152)
3	HGSV	ss82923923	Oct 12, 2018 (152)
4	HGSV	ss83001034	Oct 12, 2018 (152)
5	HUMANGENOME_JCVI	ss95681340	Oct 12, 2018 (152)
6	BCMHGSC_JDW	ss103589333	Feb 23, 2009 (130)
7	PJP	ss294894891	May 09, 2011 (137)
8	PJP	ss294894892	May 09, 2011 (135)
9	1000GENOMES	ss1376036010	Aug 21, 2014 (142)
10	SWEGEN	ss3014746174	Nov 08, 2017 (151)
11	MCHAISSO	ss3063850501	Nov 08, 2017 (151)
12	MCHAISSO	ss3064691655	Nov 08, 2017 (151)
13	MCHAISSO	ss3065627685	Nov 08, 2017 (151)
14	EVA_DECODE	ss3699543657	Jul 13, 2019 (153)
15	EVA_DECODE	ss3699543658	Jul 13, 2019 (153)
16	EVA_DECODE	ss3699543659	Jul 13, 2019 (153)
17	EVA_DECODE	ss3699543660	Jul 13, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3819386966	Jul 13, 2019 (153)
19	EVA	ss3834637683	Apr 27, 2020 (154)
20	EVA	ss3840924320	Apr 27, 2020 (154)
21	EVA	ss3846416853	Apr 27, 2020 (154)
22	GNOMAD	ss4303535146	Apr 26, 2021 (155)
23	GNOMAD	ss4303535147	Apr 26, 2021 (155)
24	GNOMAD	ss4303535148	Apr 26, 2021 (155)
25	GNOMAD	ss4303535149	Apr 26, 2021 (155)
26	GNOMAD	ss4303535150	Apr 26, 2021 (155)
27	GNOMAD	ss4303535151	Apr 26, 2021 (155)
28	GNOMAD	ss4303535152	Apr 26, 2021 (155)
29	GNOMAD	ss4303535153	Apr 26, 2021 (155)
30	GNOMAD	ss4303535154	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5220239919	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5220239920	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5220239921	Apr 26, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5301457603	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5301457604	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5301457605	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5301457606	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5301457607	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5301457608	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5494751207	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5494751208	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5494751209	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5494751210	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5494751211	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5775446203	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5775446204	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5775446205	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5775446207	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5775446208	Oct 16, 2022 (156)
50	1000Genomes	NC_000016.9 - 72172812	Oct 12, 2018 (152)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493791626 (NC_000016.10:72138912::A 42090/110510) Row 493791627 (NC_000016.10:72138912::AA 7403/110572) Row 493791628 (NC_000016.10:72138912::AAA 2818/110656)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493791626 (NC_000016.10:72138912::A 42090/110510) Row 493791627 (NC_000016.10:72138912::AA 7403/110572) Row 493791628 (NC_000016.10:72138912::AAA 2818/110656)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493791626 (NC_000016.10:72138912::A 42090/110510) Row 493791627 (NC_000016.10:72138912::AA 7403/110572) Row 493791628 (NC_000016.10:72138912::AAA 2818/110656)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493791626 (NC_000016.10:72138912::A 42090/110510) Row 493791627 (NC_000016.10:72138912::AA 7403/110572) Row 493791628 (NC_000016.10:72138912::AAA 2818/110656)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493791626 (NC_000016.10:72138912::A 42090/110510) Row 493791627 (NC_000016.10:72138912::AA 7403/110572) Row 493791628 (NC_000016.10:72138912::AAA 2818/110656)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493791626 (NC_000016.10:72138912::A 42090/110510) Row 493791627 (NC_000016.10:72138912::AA 7403/110572) Row 493791628 (NC_000016.10:72138912::AAA 2818/110656)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493791626 (NC_000016.10:72138912::A 42090/110510) Row 493791627 (NC_000016.10:72138912::AA 7403/110572) Row 493791628 (NC_000016.10:72138912::AAA 2818/110656)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493791626 (NC_000016.10:72138912::A 42090/110510) Row 493791627 (NC_000016.10:72138912::AA 7403/110572) Row 493791628 (NC_000016.10:72138912::AAA 2818/110656)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493791626 (NC_000016.10:72138912::A 42090/110510) Row 493791627 (NC_000016.10:72138912::AA 7403/110572) Row 493791628 (NC_000016.10:72138912::AAA 2818/110656)...	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 78209226 (NC_000016.9:72172811::A 6212/16726) Row 78209227 (NC_000016.9:72172811:A: 406/16726) Row 78209228 (NC_000016.9:72172811::AA 55/16726)	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 78209226 (NC_000016.9:72172811::A 6212/16726) Row 78209227 (NC_000016.9:72172811:A: 406/16726) Row 78209228 (NC_000016.9:72172811::AA 55/16726)	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 78209226 (NC_000016.9:72172811::A 6212/16726) Row 78209227 (NC_000016.9:72172811:A: 406/16726) Row 78209228 (NC_000016.9:72172811::AA 55/16726)	-	Apr 26, 2021 (155)
63	14KJPN Submission ignored due to conflicting rows: Row 109283307 (NC_000016.10:72138912::A 10586/28258) Row 109283308 (NC_000016.10:72138912:A: 672/28258) Row 109283309 (NC_000016.10:72138912::AA 93/28258)...	-	Oct 16, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 109283307 (NC_000016.10:72138912::A 10586/28258) Row 109283308 (NC_000016.10:72138912:A: 672/28258) Row 109283309 (NC_000016.10:72138912::AA 93/28258)...	-	Oct 16, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 109283307 (NC_000016.10:72138912::A 10586/28258) Row 109283308 (NC_000016.10:72138912:A: 672/28258) Row 109283309 (NC_000016.10:72138912::AA 93/28258)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 109283307 (NC_000016.10:72138912::A 10586/28258) Row 109283308 (NC_000016.10:72138912:A: 672/28258) Row 109283309 (NC_000016.10:72138912::AA 93/28258)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 109283307 (NC_000016.10:72138912::A 10586/28258) Row 109283308 (NC_000016.10:72138912:A: 672/28258) Row 109283309 (NC_000016.10:72138912::AA 93/28258)...	-	Oct 16, 2022 (156)
68	ALFA	NC_000016.10 - 72138913	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)
rs59020601	May 26, 2008 (130)
rs139775201	Sep 17, 2011 (135)
rs143865661	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11883000347	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4303535154, ss5301457608, ss5775446207	NC_000016.10:72138912:AA:	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
11883000347	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss103589333	NT_010498.15:25787024:AA:	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3014746174, ss5220239920	NC_000016.9:72172811:A:	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3699543660, ss4303535153, ss5301457605, ss5494751207, ss5775446204	NC_000016.10:72138912:A:	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
11883000347	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss294894891	NC_000016.8:70730313::A	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss294894892	NC_000016.8:70730328::A	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
69990382, ss1376036010, ss3834637683, ss3840924320, ss5220239919	NC_000016.9:72172811::A	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3063850501, ss3064691655, ss3065627685, ss3819386966, ss3846416853, ss4303535146, ss5301457603, ss5494751208, ss5775446203	NC_000016.10:72138912::A	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
11883000347	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3699543659	NC_000016.10:72138913::A	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss40677876, ss81133557, ss82923923, ss83001034, ss95681340	NT_010498.15:25787026::A	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5220239921	NC_000016.9:72172811::AA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4303535147, ss5301457606, ss5494751209, ss5775446205	NC_000016.10:72138912::AA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
11883000347	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3699543658	NC_000016.10:72138913::AA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4303535148, ss5301457607, ss5494751210, ss5775446208	NC_000016.10:72138912::AAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
11883000347	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3699543657	NC_000016.10:72138913::AAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4303535149, ss5301457604, ss5494751211	NC_000016.10:72138912::AAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
11883000347	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
11883000347	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4303535150	NC_000016.10:72138912::AAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4303535151	NC_000016.10:72138912::AAAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4303535152	NC_000016.10:72138912::AAAAAAAAA	NC_000016.10:72138912:AAAAAAAAAAAA… NC_000016.10:72138912:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs35349842

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

rs35349842