Name: rs35606607
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.

rs35606607

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:90027090-90027103 (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: delTTT / delTT / delT / dupT / dup…
delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1117 (1092/9780, ALFA)
dupT=0.3163 (1584/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GAS8 : 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	9780	TTTTTTTTTTTTTT=0.8881	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.1117, TTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	0.821399	0.044599	0.134002	32
European	Sub	8080	TTTTTTTTTTTTTT=0.8647	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.1350, TTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	0.784052	0.053987	0.161961	32
African	Sub	982	TTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	40	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	942	TTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	80	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	62	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	50	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	336	TTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	34	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	218	TTTTTTTTTTTTTT=0.995	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.005, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	0.990826	0.0	0.009174	0

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
Allele Frequency Aggregator	Total	Global	9780	(T)₁₄=0.8881	delTT=0.0000, delT=0.0000, dupT=0.1117, dupTT=0.0002, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	8080	(T)₁₄=0.8647	delTT=0.0000, delT=0.0000, dupT=0.1350, dupTT=0.0002, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	982	(T)₁₄=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	336	(T)₁₄=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	218	(T)₁₄=0.995	delTT=0.000, delT=0.000, dupT=0.005, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Asian	Sub	80	(T)₁₄=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	50	(T)₁₄=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	34	(T)₁₄=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.3163
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.3260
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.1786
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.3270
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.447
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.298

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.90027101_90027103del
GRCh38.p14 chr 16	NC_000016.10:g.90027102_90027103del
GRCh38.p14 chr 16	NC_000016.10:g.90027103del
GRCh38.p14 chr 16	NC_000016.10:g.90027103dup
GRCh38.p14 chr 16	NC_000016.10:g.90027102_90027103dup
GRCh38.p14 chr 16	NC_000016.10:g.90027101_90027103dup
GRCh38.p14 chr 16	NC_000016.10:g.90027100_90027103dup
GRCh38.p14 chr 16	NC_000016.10:g.90027094_90027103dup
GRCh37.p13 chr 16	NC_000016.9:g.90093509_90093511del
GRCh37.p13 chr 16	NC_000016.9:g.90093510_90093511del
GRCh37.p13 chr 16	NC_000016.9:g.90093511del
GRCh37.p13 chr 16	NC_000016.9:g.90093511dup
GRCh37.p13 chr 16	NC_000016.9:g.90093510_90093511dup
GRCh37.p13 chr 16	NC_000016.9:g.90093509_90093511dup
GRCh37.p13 chr 16	NC_000016.9:g.90093508_90093511dup
GRCh37.p13 chr 16	NC_000016.9:g.90093502_90093511dup
GAS8 RefSeqGene	NG_046598.1:g.12473_12475del
GAS8 RefSeqGene	NG_046598.1:g.12474_12475del
GAS8 RefSeqGene	NG_046598.1:g.12475del
GAS8 RefSeqGene	NG_046598.1:g.12475dup
GAS8 RefSeqGene	NG_046598.1:g.12474_12475dup
GAS8 RefSeqGene	NG_046598.1:g.12473_12475dup
GAS8 RefSeqGene	NG_046598.1:g.12472_12475dup
GAS8 RefSeqGene	NG_046598.1:g.12466_12475dup
GAS8-AS1 RefSeqGene	NG_054714.1:g.7810_7812del
GAS8-AS1 RefSeqGene	NG_054714.1:g.7811_7812del
GAS8-AS1 RefSeqGene	NG_054714.1:g.7812del
GAS8-AS1 RefSeqGene	NG_054714.1:g.7812dup
GAS8-AS1 RefSeqGene	NG_054714.1:g.7811_7812dup
GAS8-AS1 RefSeqGene	NG_054714.1:g.7810_7812dup
GAS8-AS1 RefSeqGene	NG_054714.1:g.7809_7812dup
GAS8-AS1 RefSeqGene	NG_054714.1:g.7803_7812dup

Gene: GAS8, growth arrest specific 8 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GAS8 transcript variant 3	NM_001286205.2:c.-369-535… NM_001286205.2:c.-369-535_-369-533del	N/A	Intron Variant
GAS8 transcript variant 4	NM_001286208.2:c.-641-535… NM_001286208.2:c.-641-535_-641-533del	N/A	Intron Variant
GAS8 transcript variant 5	NM_001286209.2:c.-72-535_… NM_001286209.2:c.-72-535_-72-533del	N/A	Intron Variant
GAS8 transcript variant 1	NM_001481.3:c.4-535_4-533… NM_001481.3:c.4-535_4-533del	N/A	Intron Variant
GAS8 transcript variant X2	XM_011522992.3:c.-268-408… XM_011522992.3:c.-268-4089_-268-4087del	N/A	Intron Variant
GAS8 transcript variant X1	XM_006721175.4:c.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₁₄=	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₁₀
GRCh38.p14 chr 16	NC_000016.10:g.90027090_90027103=	NC_000016.10:g.90027101_90027103del	NC_000016.10:g.90027102_90027103del	NC_000016.10:g.90027103del	NC_000016.10:g.90027103dup	NC_000016.10:g.90027102_90027103dup	NC_000016.10:g.90027101_90027103dup	NC_000016.10:g.90027100_90027103dup	NC_000016.10:g.90027094_90027103dup
GRCh37.p13 chr 16	NC_000016.9:g.90093498_90093511=	NC_000016.9:g.90093509_90093511del	NC_000016.9:g.90093510_90093511del	NC_000016.9:g.90093511del	NC_000016.9:g.90093511dup	NC_000016.9:g.90093510_90093511dup	NC_000016.9:g.90093509_90093511dup	NC_000016.9:g.90093508_90093511dup	NC_000016.9:g.90093502_90093511dup
GAS8 RefSeqGene	NG_046598.1:g.12462_12475=	NG_046598.1:g.12473_12475del	NG_046598.1:g.12474_12475del	NG_046598.1:g.12475del	NG_046598.1:g.12475dup	NG_046598.1:g.12474_12475dup	NG_046598.1:g.12473_12475dup	NG_046598.1:g.12472_12475dup	NG_046598.1:g.12466_12475dup
GAS8-AS1 RefSeqGene	NG_054714.1:g.7799_7812=	NG_054714.1:g.7810_7812del	NG_054714.1:g.7811_7812del	NG_054714.1:g.7812del	NG_054714.1:g.7812dup	NG_054714.1:g.7811_7812dup	NG_054714.1:g.7810_7812dup	NG_054714.1:g.7809_7812dup	NG_054714.1:g.7803_7812dup
GAS8 transcript variant 3	NM_001286205.2:c.-369-546=	NM_001286205.2:c.-369-535_-369-533del	NM_001286205.2:c.-369-534_-369-533del	NM_001286205.2:c.-369-533del	NM_001286205.2:c.-369-533dup	NM_001286205.2:c.-369-534_-369-533dup	NM_001286205.2:c.-369-535_-369-533dup	NM_001286205.2:c.-369-536_-369-533dup	NM_001286205.2:c.-369-542_-369-533dup
GAS8 transcript variant 4	NM_001286208.2:c.-641-546=	NM_001286208.2:c.-641-535_-641-533del	NM_001286208.2:c.-641-534_-641-533del	NM_001286208.2:c.-641-533del	NM_001286208.2:c.-641-533dup	NM_001286208.2:c.-641-534_-641-533dup	NM_001286208.2:c.-641-535_-641-533dup	NM_001286208.2:c.-641-536_-641-533dup	NM_001286208.2:c.-641-542_-641-533dup
GAS8 transcript variant 5	NM_001286209.2:c.-72-546=	NM_001286209.2:c.-72-535_-72-533del	NM_001286209.2:c.-72-534_-72-533del	NM_001286209.2:c.-72-533del	NM_001286209.2:c.-72-533dup	NM_001286209.2:c.-72-534_-72-533dup	NM_001286209.2:c.-72-535_-72-533dup	NM_001286209.2:c.-72-536_-72-533dup	NM_001286209.2:c.-72-542_-72-533dup
GAS8 transcript variant 1	NM_001481.2:c.4-546=	NM_001481.2:c.4-535_4-533del	NM_001481.2:c.4-534_4-533del	NM_001481.2:c.4-533del	NM_001481.2:c.4-533dup	NM_001481.2:c.4-534_4-533dup	NM_001481.2:c.4-535_4-533dup	NM_001481.2:c.4-536_4-533dup	NM_001481.2:c.4-542_4-533dup
GAS8 transcript variant 1	NM_001481.3:c.4-546=	NM_001481.3:c.4-535_4-533del	NM_001481.3:c.4-534_4-533del	NM_001481.3:c.4-533del	NM_001481.3:c.4-533dup	NM_001481.3:c.4-534_4-533dup	NM_001481.3:c.4-535_4-533dup	NM_001481.3:c.4-536_4-533dup	NM_001481.3:c.4-542_4-533dup
GAS8 transcript variant X1	XM_005256304.1:c.-72-546=	XM_005256304.1:c.-72-535_-72-533del	XM_005256304.1:c.-72-534_-72-533del	XM_005256304.1:c.-72-533del	XM_005256304.1:c.-72-533dup	XM_005256304.1:c.-72-534_-72-533dup	XM_005256304.1:c.-72-535_-72-533dup	XM_005256304.1:c.-72-536_-72-533dup	XM_005256304.1:c.-72-542_-72-533dup
GAS8 transcript variant X3	XM_005256306.1:c.-369-546=	XM_005256306.1:c.-369-535_-369-533del	XM_005256306.1:c.-369-534_-369-533del	XM_005256306.1:c.-369-533del	XM_005256306.1:c.-369-533dup	XM_005256306.1:c.-369-534_-369-533dup	XM_005256306.1:c.-369-535_-369-533dup	XM_005256306.1:c.-369-536_-369-533dup	XM_005256306.1:c.-369-542_-369-533dup
GAS8 transcript variant X4	XM_005256307.1:c.-72-546=	XM_005256307.1:c.-72-535_-72-533del	XM_005256307.1:c.-72-534_-72-533del	XM_005256307.1:c.-72-533del	XM_005256307.1:c.-72-533dup	XM_005256307.1:c.-72-534_-72-533dup	XM_005256307.1:c.-72-535_-72-533dup	XM_005256307.1:c.-72-536_-72-533dup	XM_005256307.1:c.-72-542_-72-533dup
GAS8 transcript variant X5	XM_005256308.1:c.-641-546=	XM_005256308.1:c.-641-535_-641-533del	XM_005256308.1:c.-641-534_-641-533del	XM_005256308.1:c.-641-533del	XM_005256308.1:c.-641-533dup	XM_005256308.1:c.-641-534_-641-533dup	XM_005256308.1:c.-641-535_-641-533dup	XM_005256308.1:c.-641-536_-641-533dup	XM_005256308.1:c.-641-542_-641-533dup
GAS8 transcript variant X2	XM_011522992.3:c.-268-4100=	XM_011522992.3:c.-268-4089_-268-4087del	XM_011522992.3:c.-268-4088_-268-4087del	XM_011522992.3:c.-268-4087del	XM_011522992.3:c.-268-4087dup	XM_011522992.3:c.-268-4088_-268-4087dup	XM_011522992.3:c.-268-4089_-268-4087dup	XM_011522992.3:c.-268-4090_-268-4087dup	XM_011522992.3:c.-268-4096_-268-4087dup

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#.

43 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40737504	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95685440	Feb 13, 2009 (130)
3	PJP	ss294900724	May 09, 2011 (137)
4	BILGI_BIOE	ss666681106	Apr 25, 2013 (138)
5	1000GENOMES	ss1376260045	Aug 21, 2014 (142)
6	HAMMER_LAB	ss1808663325	Sep 08, 2015 (146)
7	JJLAB	ss2031320844	Sep 14, 2016 (149)
8	SYSTEMSBIOZJU	ss2628953676	Nov 08, 2017 (151)
9	SWEGEN	ss3015043113	Nov 08, 2017 (151)
10	SWEGEN	ss3015043114	Nov 08, 2017 (151)
11	URBANLAB	ss3650580136	Oct 12, 2018 (152)
12	EVA_DECODE	ss3699907891	Jul 13, 2019 (153)
13	EVA_DECODE	ss3699907892	Jul 13, 2019 (153)
14	EVA_DECODE	ss3699907893	Jul 13, 2019 (153)
15	EVA_DECODE	ss3699907894	Jul 13, 2019 (153)
16	EVA_DECODE	ss3699907895	Jul 13, 2019 (153)
17	PACBIO	ss3788124383	Jul 13, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3819614660	Jul 13, 2019 (153)
19	EVA	ss3834732834	Apr 27, 2020 (154)
20	EVA	ss3840973685	Apr 27, 2020 (154)
21	EVA	ss3846467428	Apr 27, 2020 (154)
22	KOGIC	ss3978225152	Apr 27, 2020 (154)
23	KOGIC	ss3978225153	Apr 27, 2020 (154)
24	KOGIC	ss3978225154	Apr 27, 2020 (154)
25	GNOMAD	ss4306509836	Apr 26, 2021 (155)
26	GNOMAD	ss4306509837	Apr 26, 2021 (155)
27	GNOMAD	ss4306509838	Apr 26, 2021 (155)
28	GNOMAD	ss4306509840	Apr 26, 2021 (155)
29	GNOMAD	ss4306509841	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5221072124	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5221072125	Apr 26, 2021 (155)
32	1000G_HIGH_COVERAGE	ss5302111178	Oct 17, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5302111179	Oct 17, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5302111180	Oct 17, 2022 (156)
35	HUGCELL_USP	ss5495331614	Oct 17, 2022 (156)
36	HUGCELL_USP	ss5495331615	Oct 17, 2022 (156)
37	HUGCELL_USP	ss5495331616	Oct 17, 2022 (156)
38	HUGCELL_USP	ss5495331617	Oct 17, 2022 (156)
39	TOMMO_GENOMICS	ss5776527102	Oct 17, 2022 (156)
40	TOMMO_GENOMICS	ss5776527103	Oct 17, 2022 (156)
41	YY_MCH	ss5816253972	Oct 17, 2022 (156)
42	EVA	ss5846861959	Oct 17, 2022 (156)
43	EVA	ss5980943149	Oct 17, 2022 (156)
44	1000Genomes	NC_000016.9 - 90093498	Oct 12, 2018 (152)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 499027394 (NC_000016.10:90027089::T 38295/122530) Row 499027395 (NC_000016.10:90027089::TT 1330/122600) Row 499027396 (NC_000016.10:90027089::TTT 14/122642)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 499027394 (NC_000016.10:90027089::T 38295/122530) Row 499027395 (NC_000016.10:90027089::TT 1330/122600) Row 499027396 (NC_000016.10:90027089::TTT 14/122642)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 499027394 (NC_000016.10:90027089::T 38295/122530) Row 499027395 (NC_000016.10:90027089::TT 1330/122600) Row 499027396 (NC_000016.10:90027089::TTT 14/122642)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 499027394 (NC_000016.10:90027089::T 38295/122530) Row 499027395 (NC_000016.10:90027089::TT 1330/122600) Row 499027396 (NC_000016.10:90027089::TTT 14/122642)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 499027394 (NC_000016.10:90027089::T 38295/122530) Row 499027395 (NC_000016.10:90027089::TT 1330/122600) Row 499027396 (NC_000016.10:90027089::TTT 14/122642)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 499027394 (NC_000016.10:90027089::T 38295/122530) Row 499027395 (NC_000016.10:90027089::TT 1330/122600) Row 499027396 (NC_000016.10:90027089::TTT 14/122642)...	-	Apr 26, 2021 (155)
51	Korean Genome Project Submission ignored due to conflicting rows: Row 34603153 (NC_000016.10:90027090::T 382/1828) Row 34603154 (NC_000016.10:90027089:T: 36/1828) Row 34603155 (NC_000016.10:90027090::TT 14/1828)	-	Apr 27, 2020 (154)
52	Korean Genome Project Submission ignored due to conflicting rows: Row 34603153 (NC_000016.10:90027090::T 382/1828) Row 34603154 (NC_000016.10:90027089:T: 36/1828) Row 34603155 (NC_000016.10:90027090::TT 14/1828)	-	Apr 27, 2020 (154)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 34603153 (NC_000016.10:90027090::T 382/1828) Row 34603154 (NC_000016.10:90027089:T: 36/1828) Row 34603155 (NC_000016.10:90027090::TT 14/1828)	-	Apr 27, 2020 (154)
54	8.3KJPN Submission ignored due to conflicting rows: Row 79041431 (NC_000016.9:90093497::T 3342/16724) Row 79041432 (NC_000016.9:90093497::TT 1/16724)	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 79041431 (NC_000016.9:90093497::T 3342/16724) Row 79041432 (NC_000016.9:90093497::TT 1/16724)	-	Apr 26, 2021 (155)
56	14KJPN Submission ignored due to conflicting rows: Row 110364206 (NC_000016.10:90027089::T 5444/28244) Row 110364207 (NC_000016.10:90027089::TT 2/28244)	-	Oct 17, 2022 (156)
57	14KJPN Submission ignored due to conflicting rows: Row 110364206 (NC_000016.10:90027089::T 5444/28244) Row 110364207 (NC_000016.10:90027089::TT 2/28244)	-	Oct 17, 2022 (156)
58	ALFA	NC_000016.10 - 90027090	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)
rs71782937	May 11, 2012 (137)
rs149866103	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4306509841	NC_000016.10:90027089:TTT:	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3699907891, ss4306509840, ss5495331617	NC_000016.10:90027089:TT:	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
3559630929	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3788124383	NC_000016.9:90093497:T:	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3978225153, ss5302111179, ss5495331616	NC_000016.10:90027089:T:	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3559630929	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3699907892	NC_000016.10:90027090:T:	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss294900724	NC_000016.8:88621006::T	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
70767197, ss666681106, ss1376260045, ss1808663325, ss2031320844, ss2628953676, ss3015043113, ss3834732834, ss3840973685, ss5221072124, ss5846861959, ss5980943149	NC_000016.9:90093497::T	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3650580136, ss3819614660, ss3846467428, ss4306509836, ss5302111178, ss5495331614, ss5776527102, ss5816253972	NC_000016.10:90027089::T	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3559630929	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3978225152	NC_000016.10:90027090::T	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3699907893	NC_000016.10:90027091::T	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss40737504	NT_010542.15:1654114::T	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss95685440	NT_010542.15:1654128::T	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3015043114, ss5221072125	NC_000016.9:90093497::TT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4306509837, ss5302111180, ss5495331615, ss5776527103	NC_000016.10:90027089::TT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
3559630929	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3978225154	NC_000016.10:90027090::TT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3699907894	NC_000016.10:90027091::TT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4306509838	NC_000016.10:90027089::TTT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3559630929	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3559630929	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3699907895	NC_000016.10:90027091::TTTTTTTTTT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3255054217	NC_000016.10:90027089::TTTT	NC_000016.10:90027089:TTTTTTTTTTTT… NC_000016.10:90027089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs35606607

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

rs35606607