Name: rs35283042
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.

rs35283042

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:72117035-72117054 (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)₁₀ / del(A)₇ / del(A)₆ / del…
del(A)₁₀ / del(A)₇ / del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₀=0.000004 (1/264690, TOPMED)
del(A)₁₀=0.0000 (0/2132, ALFA)
del(A)₇=0.0000 (0/2132, ALFA) (+ 9 more)
del(A)₆=0.0000 (0/2132, ALFA)
del(A)₄=0.0000 (0/2132, ALFA)
delAA=0.0000 (0/2132, ALFA)
delA=0.0000 (0/2132, ALFA)
dupA=0.0000 (0/2132, ALFA)
dupAA=0.0000 (0/2132, ALFA)
dupAAA=0.0000 (0/2132, ALFA)
dup(A)₄=0.0000 (0/2132, ALFA)
dup(A)₅=0.0000 (0/2132, 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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(A)₂₀=0.999996	del(A)₁₀=0.000004
Allele Frequency Aggregator	Total	Global	2132	(A)₂₀=1.0000	del(A)₁₀=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, 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	1566	(A)₂₀=1.0000	del(A)₁₀=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, 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	208	(A)₂₀=1.000	del(A)₁₀=0.000, del(A)₇=0.000, del(A)₆=0.000, 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	178	(A)₂₀=1.000	del(A)₁₀=0.000, del(A)₇=0.000, del(A)₆=0.000, 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	86	(A)₂₀=1.00	del(A)₁₀=0.00, del(A)₇=0.00, del(A)₆=0.00, 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	Latin American 1	Sub	38	(A)₂₀=1.00	del(A)₁₀=0.00, del(A)₇=0.00, del(A)₆=0.00, 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	36	(A)₂₀=1.00	del(A)₁₀=0.00, del(A)₇=0.00, del(A)₆=0.00, 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	20	(A)₂₀=1.00	del(A)₁₀=0.00, del(A)₇=0.00, del(A)₆=0.00, 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.72117045_72117054del
GRCh38.p14 chr 16	NC_000016.10:g.72117048_72117054del
GRCh38.p14 chr 16	NC_000016.10:g.72117049_72117054del
GRCh38.p14 chr 16	NC_000016.10:g.72117051_72117054del
GRCh38.p14 chr 16	NC_000016.10:g.72117052_72117054del
GRCh38.p14 chr 16	NC_000016.10:g.72117053_72117054del
GRCh38.p14 chr 16	NC_000016.10:g.72117054del
GRCh38.p14 chr 16	NC_000016.10:g.72117054dup
GRCh38.p14 chr 16	NC_000016.10:g.72117053_72117054dup
GRCh38.p14 chr 16	NC_000016.10:g.72117052_72117054dup
GRCh38.p14 chr 16	NC_000016.10:g.72117051_72117054dup
GRCh38.p14 chr 16	NC_000016.10:g.72117050_72117054dup
GRCh38.p14 chr 16	NC_000016.10:g.72117044_72117054dup
GRCh37.p13 chr 16	NC_000016.9:g.72150944_72150953del
GRCh37.p13 chr 16	NC_000016.9:g.72150947_72150953del
GRCh37.p13 chr 16	NC_000016.9:g.72150948_72150953del
GRCh37.p13 chr 16	NC_000016.9:g.72150950_72150953del
GRCh37.p13 chr 16	NC_000016.9:g.72150951_72150953del
GRCh37.p13 chr 16	NC_000016.9:g.72150952_72150953del
GRCh37.p13 chr 16	NC_000016.9:g.72150953del
GRCh37.p13 chr 16	NC_000016.9:g.72150953dup
GRCh37.p13 chr 16	NC_000016.9:g.72150952_72150953dup
GRCh37.p13 chr 16	NC_000016.9:g.72150951_72150953dup
GRCh37.p13 chr 16	NC_000016.9:g.72150950_72150953dup
GRCh37.p13 chr 16	NC_000016.9:g.72150949_72150953dup
GRCh37.p13 chr 16	NC_000016.9:g.72150943_72150953dup

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.	N/A	Genic Downstream Transcript Variant
PMFBP1 transcript variant 1	NM_031293.3:c.	N/A	Genic Downstream Transcript Variant
PMFBP1 transcript variant X1	XM_011523357.4:c.3083-14_… XM_011523357.4:c.3083-14_3083-5del	N/A	Intron Variant
PMFBP1 transcript variant X2	XM_011523358.4:c.3083-14_… XM_011523358.4:c.3083-14_3083-5del	N/A	Intron Variant
PMFBP1 transcript variant X3	XM_011523360.4:c.3083-14_… XM_011523360.4:c.3083-14_3083-5del	N/A	Intron Variant
PMFBP1 transcript variant X4	XM_011523361.4:c.3083-14_… XM_011523361.4:c.3083-14_3083-5del	N/A	Intron Variant
PMFBP1 transcript variant X5	XM_011523362.4:c.3074-14_… XM_011523362.4:c.3074-14_3074-5del	N/A	Intron Variant
PMFBP1 transcript variant X6	XM_047434734.1:c.3023-14_… XM_047434734.1:c.3023-14_3023-5del	N/A	Intron Variant
PMFBP1 transcript variant X7	XM_047434735.1:c.2378-14_… XM_047434735.1:c.2378-14_2378-5del	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)₁₀	del(A)₇	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₁₁
GRCh38.p14 chr 16	NC_000016.10:g.72117035_72117054=	NC_000016.10:g.72117045_72117054del	NC_000016.10:g.72117048_72117054del	NC_000016.10:g.72117049_72117054del	NC_000016.10:g.72117051_72117054del	NC_000016.10:g.72117052_72117054del	NC_000016.10:g.72117053_72117054del	NC_000016.10:g.72117054del	NC_000016.10:g.72117054dup	NC_000016.10:g.72117053_72117054dup	NC_000016.10:g.72117052_72117054dup	NC_000016.10:g.72117051_72117054dup	NC_000016.10:g.72117050_72117054dup	NC_000016.10:g.72117044_72117054dup
GRCh37.p13 chr 16	NC_000016.9:g.72150934_72150953=	NC_000016.9:g.72150944_72150953del	NC_000016.9:g.72150947_72150953del	NC_000016.9:g.72150948_72150953del	NC_000016.9:g.72150950_72150953del	NC_000016.9:g.72150951_72150953del	NC_000016.9:g.72150952_72150953del	NC_000016.9:g.72150953del	NC_000016.9:g.72150953dup	NC_000016.9:g.72150952_72150953dup	NC_000016.9:g.72150951_72150953dup	NC_000016.9:g.72150950_72150953dup	NC_000016.9:g.72150949_72150953dup	NC_000016.9:g.72150943_72150953dup
PMFBP1 transcript variant X1	XM_011523357.4:c.3083-5=	XM_011523357.4:c.3083-14_3083-5del	XM_011523357.4:c.3083-11_3083-5del	XM_011523357.4:c.3083-10_3083-5del	XM_011523357.4:c.3083-8_3083-5del	XM_011523357.4:c.3083-7_3083-5del	XM_011523357.4:c.3083-6_3083-5del	XM_011523357.4:c.3083-5del	XM_011523357.4:c.3083-5dup	XM_011523357.4:c.3083-6_3083-5dup	XM_011523357.4:c.3083-7_3083-5dup	XM_011523357.4:c.3083-8_3083-5dup	XM_011523357.4:c.3083-9_3083-5dup	XM_011523357.4:c.3083-15_3083-5dup
PMFBP1 transcript variant X2	XM_011523358.4:c.3083-5=	XM_011523358.4:c.3083-14_3083-5del	XM_011523358.4:c.3083-11_3083-5del	XM_011523358.4:c.3083-10_3083-5del	XM_011523358.4:c.3083-8_3083-5del	XM_011523358.4:c.3083-7_3083-5del	XM_011523358.4:c.3083-6_3083-5del	XM_011523358.4:c.3083-5del	XM_011523358.4:c.3083-5dup	XM_011523358.4:c.3083-6_3083-5dup	XM_011523358.4:c.3083-7_3083-5dup	XM_011523358.4:c.3083-8_3083-5dup	XM_011523358.4:c.3083-9_3083-5dup	XM_011523358.4:c.3083-15_3083-5dup
PMFBP1 transcript variant X3	XM_011523360.4:c.3083-5=	XM_011523360.4:c.3083-14_3083-5del	XM_011523360.4:c.3083-11_3083-5del	XM_011523360.4:c.3083-10_3083-5del	XM_011523360.4:c.3083-8_3083-5del	XM_011523360.4:c.3083-7_3083-5del	XM_011523360.4:c.3083-6_3083-5del	XM_011523360.4:c.3083-5del	XM_011523360.4:c.3083-5dup	XM_011523360.4:c.3083-6_3083-5dup	XM_011523360.4:c.3083-7_3083-5dup	XM_011523360.4:c.3083-8_3083-5dup	XM_011523360.4:c.3083-9_3083-5dup	XM_011523360.4:c.3083-15_3083-5dup
PMFBP1 transcript variant X4	XM_011523361.4:c.3083-5=	XM_011523361.4:c.3083-14_3083-5del	XM_011523361.4:c.3083-11_3083-5del	XM_011523361.4:c.3083-10_3083-5del	XM_011523361.4:c.3083-8_3083-5del	XM_011523361.4:c.3083-7_3083-5del	XM_011523361.4:c.3083-6_3083-5del	XM_011523361.4:c.3083-5del	XM_011523361.4:c.3083-5dup	XM_011523361.4:c.3083-6_3083-5dup	XM_011523361.4:c.3083-7_3083-5dup	XM_011523361.4:c.3083-8_3083-5dup	XM_011523361.4:c.3083-9_3083-5dup	XM_011523361.4:c.3083-15_3083-5dup
PMFBP1 transcript variant X5	XM_011523362.4:c.3074-5=	XM_011523362.4:c.3074-14_3074-5del	XM_011523362.4:c.3074-11_3074-5del	XM_011523362.4:c.3074-10_3074-5del	XM_011523362.4:c.3074-8_3074-5del	XM_011523362.4:c.3074-7_3074-5del	XM_011523362.4:c.3074-6_3074-5del	XM_011523362.4:c.3074-5del	XM_011523362.4:c.3074-5dup	XM_011523362.4:c.3074-6_3074-5dup	XM_011523362.4:c.3074-7_3074-5dup	XM_011523362.4:c.3074-8_3074-5dup	XM_011523362.4:c.3074-9_3074-5dup	XM_011523362.4:c.3074-15_3074-5dup
PMFBP1 transcript variant X6	XM_047434734.1:c.3023-5=	XM_047434734.1:c.3023-14_3023-5del	XM_047434734.1:c.3023-11_3023-5del	XM_047434734.1:c.3023-10_3023-5del	XM_047434734.1:c.3023-8_3023-5del	XM_047434734.1:c.3023-7_3023-5del	XM_047434734.1:c.3023-6_3023-5del	XM_047434734.1:c.3023-5del	XM_047434734.1:c.3023-5dup	XM_047434734.1:c.3023-6_3023-5dup	XM_047434734.1:c.3023-7_3023-5dup	XM_047434734.1:c.3023-8_3023-5dup	XM_047434734.1:c.3023-9_3023-5dup	XM_047434734.1:c.3023-15_3023-5dup
PMFBP1 transcript variant X7	XM_047434735.1:c.2378-5=	XM_047434735.1:c.2378-14_2378-5del	XM_047434735.1:c.2378-11_2378-5del	XM_047434735.1:c.2378-10_2378-5del	XM_047434735.1:c.2378-8_2378-5del	XM_047434735.1:c.2378-7_2378-5del	XM_047434735.1:c.2378-6_2378-5del	XM_047434735.1:c.2378-5del	XM_047434735.1:c.2378-5dup	XM_047434735.1:c.2378-6_2378-5dup	XM_047434735.1:c.2378-7_2378-5dup	XM_047434735.1:c.2378-8_2378-5dup	XM_047434735.1:c.2378-9_2378-5dup	XM_047434735.1:c.2378-15_2378-5dup

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#.

53 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40736930	Mar 14, 2006 (126)
2	HGSV	ss80470038	Dec 16, 2007 (130)
3	HGSV	ss81552788	Dec 16, 2007 (130)
4	HGSV	ss83378597	Dec 16, 2007 (130)
5	HUMANGENOME_JCVI	ss95681332	Feb 05, 2009 (130)
6	PJP	ss294894877	May 09, 2011 (137)
7	PJP	ss294894878	May 09, 2011 (134)
8	BILGI_BIOE	ss666676581	Apr 25, 2013 (138)
9	MCHAISSO	ss3063850494	Nov 08, 2017 (151)
10	MCHAISSO	ss3064691647	Nov 08, 2017 (151)
11	MCHAISSO	ss3065627678	Nov 08, 2017 (151)
12	URBANLAB	ss3650538370	Oct 12, 2018 (152)
13	EVA_DECODE	ss3699543335	Jul 13, 2019 (153)
14	EVA_DECODE	ss3699543336	Jul 13, 2019 (153)
15	EVA_DECODE	ss3699543337	Jul 13, 2019 (153)
16	EVA_DECODE	ss3699543338	Jul 13, 2019 (153)
17	EVA_DECODE	ss3699543339	Jul 13, 2019 (153)
18	PACBIO	ss3793051862	Jul 13, 2019 (153)
19	PACBIO	ss3797936947	Jul 13, 2019 (153)
20	EVA	ss3834637606	Apr 27, 2020 (154)
21	EVA	ss3846416803	Apr 27, 2020 (154)
22	KOGIC	ss3977871984	Apr 27, 2020 (154)
23	KOGIC	ss3977871985	Apr 27, 2020 (154)
24	KOGIC	ss3977871986	Apr 27, 2020 (154)
25	KOGIC	ss3977871987	Apr 27, 2020 (154)
26	GNOMAD	ss4303532486	Apr 26, 2021 (155)
27	GNOMAD	ss4303532487	Apr 26, 2021 (155)
28	GNOMAD	ss4303532488	Apr 26, 2021 (155)
29	GNOMAD	ss4303532489	Apr 26, 2021 (155)
30	GNOMAD	ss4303532490	Apr 26, 2021 (155)
31	GNOMAD	ss4303532491	Apr 26, 2021 (155)
32	GNOMAD	ss4303532492	Apr 26, 2021 (155)
33	GNOMAD	ss4303532493	Apr 26, 2021 (155)
34	GNOMAD	ss4303532494	Apr 26, 2021 (155)
35	TOPMED	ss5020417010	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5220239293	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5220239294	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5220239295	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5301457182	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5301457183	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5301457184	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5301457185	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5494750803	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5494750804	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5494750806	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5775445375	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5775445377	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5775445378	Oct 16, 2022 (156)
49	EVA	ss5800202279	Oct 16, 2022 (156)
50	EVA	ss5846601810	Oct 16, 2022 (156)
51	EVA	ss5846601811	Oct 16, 2022 (156)
52	EVA	ss5846601812	Oct 16, 2022 (156)
53	EVA	ss5851621768	Oct 16, 2022 (156)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493787236 (NC_000016.10:72117034::A 62833/107450) Row 493787237 (NC_000016.10:72117034::AA 6864/107218) Row 493787238 (NC_000016.10:72117034::AAA 597/107428)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493787236 (NC_000016.10:72117034::A 62833/107450) Row 493787237 (NC_000016.10:72117034::AA 6864/107218) Row 493787238 (NC_000016.10:72117034::AAA 597/107428)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493787236 (NC_000016.10:72117034::A 62833/107450) Row 493787237 (NC_000016.10:72117034::AA 6864/107218) Row 493787238 (NC_000016.10:72117034::AAA 597/107428)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493787236 (NC_000016.10:72117034::A 62833/107450) Row 493787237 (NC_000016.10:72117034::AA 6864/107218) Row 493787238 (NC_000016.10:72117034::AAA 597/107428)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493787236 (NC_000016.10:72117034::A 62833/107450) Row 493787237 (NC_000016.10:72117034::AA 6864/107218) Row 493787238 (NC_000016.10:72117034::AAA 597/107428)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493787236 (NC_000016.10:72117034::A 62833/107450) Row 493787237 (NC_000016.10:72117034::AA 6864/107218) Row 493787238 (NC_000016.10:72117034::AAA 597/107428)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493787236 (NC_000016.10:72117034::A 62833/107450) Row 493787237 (NC_000016.10:72117034::AA 6864/107218) Row 493787238 (NC_000016.10:72117034::AAA 597/107428)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493787236 (NC_000016.10:72117034::A 62833/107450) Row 493787237 (NC_000016.10:72117034::AA 6864/107218) Row 493787238 (NC_000016.10:72117034::AAA 597/107428)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 493787236 (NC_000016.10:72117034::A 62833/107450) Row 493787237 (NC_000016.10:72117034::AA 6864/107218) Row 493787238 (NC_000016.10:72117034::AAA 597/107428)...	-	Apr 26, 2021 (155)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 34249985 (NC_000016.10:72117036::A 764/1818) Row 34249986 (NC_000016.10:72117036::AA 55/1818) Row 34249987 (NC_000016.10:72117035:A: 101/1818)...	-	Apr 27, 2020 (154)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 34249985 (NC_000016.10:72117036::A 764/1818) Row 34249986 (NC_000016.10:72117036::AA 55/1818) Row 34249987 (NC_000016.10:72117035:A: 101/1818)...	-	Apr 27, 2020 (154)
65	Korean Genome Project Submission ignored due to conflicting rows: Row 34249985 (NC_000016.10:72117036::A 764/1818) Row 34249986 (NC_000016.10:72117036::AA 55/1818) Row 34249987 (NC_000016.10:72117035:A: 101/1818)...	-	Apr 27, 2020 (154)
66	Korean Genome Project Submission ignored due to conflicting rows: Row 34249985 (NC_000016.10:72117036::A 764/1818) Row 34249986 (NC_000016.10:72117036::AA 55/1818) Row 34249987 (NC_000016.10:72117035:A: 101/1818)...	-	Apr 27, 2020 (154)
67	8.3KJPN Submission ignored due to conflicting rows: Row 78208600 (NC_000016.9:72150933::A 9664/16732) Row 78208601 (NC_000016.9:72150933::AA 47/16732) Row 78208602 (NC_000016.9:72150933:A: 13/16732)	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 78208600 (NC_000016.9:72150933::A 9664/16732) Row 78208601 (NC_000016.9:72150933::AA 47/16732) Row 78208602 (NC_000016.9:72150933:A: 13/16732)	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 78208600 (NC_000016.9:72150933::A 9664/16732) Row 78208601 (NC_000016.9:72150933::AA 47/16732) Row 78208602 (NC_000016.9:72150933:A: 13/16732)	-	Apr 26, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 109282479 (NC_000016.10:72117034::A 16556/28254) Row 109282481 (NC_000016.10:72117034::AA 67/28254) Row 109282482 (NC_000016.10:72117034:A: 12/28254)	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 109282479 (NC_000016.10:72117034::A 16556/28254) Row 109282481 (NC_000016.10:72117034::AA 67/28254) Row 109282482 (NC_000016.10:72117034:A: 12/28254)	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 109282479 (NC_000016.10:72117034::A 16556/28254) Row 109282481 (NC_000016.10:72117034::AA 67/28254) Row 109282482 (NC_000016.10:72117034:A: 12/28254)	-	Oct 16, 2022 (156)
73	TopMed	NC_000016.10 - 72117035	Apr 26, 2021 (155)
74	ALFA	NC_000016.10 - 72117035	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)
rs146600539	May 11, 2012 (137)
rs61291365	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
235962671, ss5020417010	NC_000016.10:72117034:AAAAAAAAAA:	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4303532494	NC_000016.10:72117034:AAAAAAA:	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4303532493	NC_000016.10:72117034:AAAAAA:	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4303532492	NC_000016.10:72117034:AAA:	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3977871987, ss4303532491	NC_000016.10:72117034:AA:	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5220239295	NC_000016.9:72150933:A:	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3699543339, ss4303532490, ss5301457185, ss5494750804, ss5775445378	NC_000016.10:72117034:A:	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3977871986	NC_000016.10:72117035:A:	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294894877	NC_000016.8:70708435::A	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss294894878	NC_000016.8:70708454::A	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss666676581, ss3793051862, ss3797936947, ss3834637606, ss5220239293, ss5800202279, ss5846601810	NC_000016.9:72150933::A	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3063850494, ss3064691647, ss3065627678, ss3650538370, ss3846416803, ss4303532486, ss5301457182, ss5494750803, ss5775445375, ss5851621768	NC_000016.10:72117034::A	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3699543338	NC_000016.10:72117035::A	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3977871984	NC_000016.10:72117036::A	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss40736930, ss81552788, ss83378597, ss95681332	NT_010498.15:25765152::A	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5220239294, ss5846601811	NC_000016.9:72150933::AA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4303532487, ss5301457183, ss5494750806, ss5775445377	NC_000016.10:72117034::AA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3699543337	NC_000016.10:72117035::AA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3977871985	NC_000016.10:72117036::AA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss80470038	NT_010498.15:25765152::AA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5846601812	NC_000016.9:72150933::AAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA
ss4303532488, ss5301457184	NC_000016.10:72117034::AAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3699543336	NC_000016.10:72117035::AAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4303532489	NC_000016.10:72117034::AAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
5434466965	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3699543335	NC_000016.10:72117035::AAAAAAAAAAA	NC_000016.10:72117034:AAAAAAAAAAAA… NC_000016.10:72117034:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs35283042

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

rs35283042