Name: rs35808845
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.

rs35808845

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:48295621-48295634 (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: delTT / delT / dupT / dupTT / dup(…
delTT / delT / dupT / dupTT / dup(T)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.03335 (397/11904, ALFA)
delT=0.1775 (889/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SKAP1 : Intron Variant
SKAP1-AS2 : 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	11904	TTTTTTTTTTTTTT=0.95951	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00714, TTTTTTTTTTTTTTT=0.03335, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000	0.938661	0.005793	0.055546	32
European	Sub	9790	TTTTTTTTTTTTTT=0.9509	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0086, TTTTTTTTTTTTTTT=0.0406, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	0.925203	0.007064	0.067733	32
African	Sub	1240	TTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	34	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1206	TTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	50	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	40	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	TTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	84	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	372	TTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	70	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	298	TTTTTTTTTTTTTT=0.997	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000	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	11904	(T)₁₄=0.95951	delTT=0.00000, delT=0.00714, dupT=0.03335, dupTT=0.00000, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	9790	(T)₁₄=0.9509	delTT=0.0000, delT=0.0086, dupT=0.0406, dupTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	1240	(T)₁₄=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	372	(T)₁₄=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	298	(T)₁₄=0.997	delTT=0.000, delT=0.003, dupT=0.000, dupTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	84	(T)₁₄=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	70	(T)₁₄=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	50	(T)₁₄=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₄=0.8225	delT=0.1775
1000Genomes	African	Sub	1322	(T)₁₄=0.6490	delT=0.3510
1000Genomes	East Asian	Sub	1008	(T)₁₄=0.9435	delT=0.0565
1000Genomes	Europe	Sub	1006	(T)₁₄=0.8797	delT=0.1203
1000Genomes	South Asian	Sub	978	(T)₁₄=0.907	delT=0.093
1000Genomes	American	Sub	694	(T)₁₄=0.775	delT=0.225

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 17	NC_000017.11:g.48295633_48295634del
GRCh38.p14 chr 17	NC_000017.11:g.48295634del
GRCh38.p14 chr 17	NC_000017.11:g.48295634dup
GRCh38.p14 chr 17	NC_000017.11:g.48295633_48295634dup
GRCh38.p14 chr 17	NC_000017.11:g.48295631_48295634dup
GRCh37.p13 chr 17	NC_000017.10:g.46372995_46372996del
GRCh37.p13 chr 17	NC_000017.10:g.46372996del
GRCh37.p13 chr 17	NC_000017.10:g.46372996dup
GRCh37.p13 chr 17	NC_000017.10:g.46372995_46372996dup
GRCh37.p13 chr 17	NC_000017.10:g.46372993_46372996dup

Gene: SKAP1, src kinase associated phosphoprotein 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SKAP1 transcript variant 2	NM_001075099.2:c.280+5028… NM_001075099.2:c.280+50283_280+50284del	N/A	Intron Variant
SKAP1 transcript variant 1	NM_003726.4:c.280+50283_2… NM_003726.4:c.280+50283_280+50284del	N/A	Intron Variant
SKAP1 transcript variant X6	XM_005257755.5:c.280+5028… XM_005257755.5:c.280+50283_280+50284del	N/A	Intron Variant
SKAP1 transcript variant X1	XM_047436972.1:c.280+5028… XM_047436972.1:c.280+50283_280+50284del	N/A	Intron Variant
SKAP1 transcript variant X2	XM_047436973.1:c.280+5028… XM_047436973.1:c.280+50283_280+50284del	N/A	Intron Variant
SKAP1 transcript variant X3	XM_047436974.1:c.232+5028… XM_047436974.1:c.232+50283_232+50284del	N/A	Intron Variant
SKAP1 transcript variant X4	XM_047436975.1:c.280+5028… XM_047436975.1:c.280+50283_280+50284del	N/A	Intron Variant
SKAP1 transcript variant X5	XM_047436976.1:c.226+5028… XM_047436976.1:c.226+50283_226+50284del	N/A	Intron Variant
SKAP1 transcript variant X7	XM_047436977.1:c.280+5028… XM_047436977.1:c.280+50283_280+50284del	N/A	Intron Variant
SKAP1 transcript variant X9	XM_047436980.1:c.-122+502… XM_047436980.1:c.-122+50283_-122+50284del	N/A	Intron Variant
SKAP1 transcript variant X8	XM_017025258.2:c.	N/A	Genic Upstream Transcript Variant
SKAP1 transcript variant X10	XM_047436978.1:c.	N/A	Genic Upstream Transcript Variant
SKAP1 transcript variant X11	XM_047436979.1:c.	N/A	Genic Upstream Transcript Variant

Gene: SKAP1-AS2, SKAP1 antisense RNA 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SKAP1-AS2 transcript variant 1	NR_131239.1:n.	N/A	Intron Variant
SKAP1-AS2 transcript variant 2	NR_131240.1:n.	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	(T)₁₄=	delTT	delT	dupT	dupTT	dup(T)₄
GRCh38.p14 chr 17	NC_000017.11:g.48295621_48295634=	NC_000017.11:g.48295633_48295634del	NC_000017.11:g.48295634del	NC_000017.11:g.48295634dup	NC_000017.11:g.48295633_48295634dup	NC_000017.11:g.48295631_48295634dup
GRCh37.p13 chr 17	NC_000017.10:g.46372983_46372996=	NC_000017.10:g.46372995_46372996del	NC_000017.10:g.46372996del	NC_000017.10:g.46372996dup	NC_000017.10:g.46372995_46372996dup	NC_000017.10:g.46372993_46372996dup
SKAP1 transcript variant 2	NM_001075099.1:c.280+50284=	NM_001075099.1:c.280+50283_280+50284del	NM_001075099.1:c.280+50284del	NM_001075099.1:c.280+50284dup	NM_001075099.1:c.280+50283_280+50284dup	NM_001075099.1:c.280+50281_280+50284dup
SKAP1 transcript variant 2	NM_001075099.2:c.280+50284=	NM_001075099.2:c.280+50283_280+50284del	NM_001075099.2:c.280+50284del	NM_001075099.2:c.280+50284dup	NM_001075099.2:c.280+50283_280+50284dup	NM_001075099.2:c.280+50281_280+50284dup
SKAP1 transcript variant 1	NM_003726.3:c.280+50284=	NM_003726.3:c.280+50283_280+50284del	NM_003726.3:c.280+50284del	NM_003726.3:c.280+50284dup	NM_003726.3:c.280+50283_280+50284dup	NM_003726.3:c.280+50281_280+50284dup
SKAP1 transcript variant 1	NM_003726.4:c.280+50284=	NM_003726.4:c.280+50283_280+50284del	NM_003726.4:c.280+50284del	NM_003726.4:c.280+50284dup	NM_003726.4:c.280+50283_280+50284dup	NM_003726.4:c.280+50281_280+50284dup
SKAP1 transcript variant X1	XM_005257754.1:c.247+50284=	XM_005257754.1:c.247+50283_247+50284del	XM_005257754.1:c.247+50284del	XM_005257754.1:c.247+50284dup	XM_005257754.1:c.247+50283_247+50284dup	XM_005257754.1:c.247+50281_247+50284dup
SKAP1 transcript variant X2	XM_005257755.1:c.280+50284=	XM_005257755.1:c.280+50283_280+50284del	XM_005257755.1:c.280+50284del	XM_005257755.1:c.280+50284dup	XM_005257755.1:c.280+50283_280+50284dup	XM_005257755.1:c.280+50281_280+50284dup
SKAP1 transcript variant X6	XM_005257755.5:c.280+50284=	XM_005257755.5:c.280+50283_280+50284del	XM_005257755.5:c.280+50284del	XM_005257755.5:c.280+50284dup	XM_005257755.5:c.280+50283_280+50284dup	XM_005257755.5:c.280+50281_280+50284dup
SKAP1 transcript variant X3	XM_005257756.1:c.-3+48636=	XM_005257756.1:c.-3+48635_-3+48636del	XM_005257756.1:c.-3+48636del	XM_005257756.1:c.-3+48636dup	XM_005257756.1:c.-3+48635_-3+48636dup	XM_005257756.1:c.-3+48633_-3+48636dup
SKAP1 transcript variant X1	XM_047436972.1:c.280+50284=	XM_047436972.1:c.280+50283_280+50284del	XM_047436972.1:c.280+50284del	XM_047436972.1:c.280+50284dup	XM_047436972.1:c.280+50283_280+50284dup	XM_047436972.1:c.280+50281_280+50284dup
SKAP1 transcript variant X2	XM_047436973.1:c.280+50284=	XM_047436973.1:c.280+50283_280+50284del	XM_047436973.1:c.280+50284del	XM_047436973.1:c.280+50284dup	XM_047436973.1:c.280+50283_280+50284dup	XM_047436973.1:c.280+50281_280+50284dup
SKAP1 transcript variant X3	XM_047436974.1:c.232+50284=	XM_047436974.1:c.232+50283_232+50284del	XM_047436974.1:c.232+50284del	XM_047436974.1:c.232+50284dup	XM_047436974.1:c.232+50283_232+50284dup	XM_047436974.1:c.232+50281_232+50284dup
SKAP1 transcript variant X4	XM_047436975.1:c.280+50284=	XM_047436975.1:c.280+50283_280+50284del	XM_047436975.1:c.280+50284del	XM_047436975.1:c.280+50284dup	XM_047436975.1:c.280+50283_280+50284dup	XM_047436975.1:c.280+50281_280+50284dup
SKAP1 transcript variant X5	XM_047436976.1:c.226+50284=	XM_047436976.1:c.226+50283_226+50284del	XM_047436976.1:c.226+50284del	XM_047436976.1:c.226+50284dup	XM_047436976.1:c.226+50283_226+50284dup	XM_047436976.1:c.226+50281_226+50284dup
SKAP1 transcript variant X7	XM_047436977.1:c.280+50284=	XM_047436977.1:c.280+50283_280+50284del	XM_047436977.1:c.280+50284del	XM_047436977.1:c.280+50284dup	XM_047436977.1:c.280+50283_280+50284dup	XM_047436977.1:c.280+50281_280+50284dup
SKAP1 transcript variant X9	XM_047436980.1:c.-122+50284=	XM_047436980.1:c.-122+50283_-122+50284del	XM_047436980.1:c.-122+50284del	XM_047436980.1:c.-122+50284dup	XM_047436980.1:c.-122+50283_-122+50284dup	XM_047436980.1:c.-122+50281_-122+50284dup

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#.

45 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40800472	Dec 03, 2013 (142)
2	HUMANGENOME_JCVI	ss95695265	Dec 05, 2013 (142)
3	HUMANGENOME_JCVI	ss96568505	Feb 13, 2009 (137)
4	GMI	ss289328042	May 04, 2012 (137)
5	PJP	ss294915349	May 09, 2011 (134)
6	SSMP	ss664360466	Apr 01, 2015 (144)
7	1000GENOMES	ss1376692779	Aug 21, 2014 (142)
8	SWEGEN	ss3015601246	Nov 08, 2017 (151)
9	MCHAISSO	ss3064712992	Nov 08, 2017 (151)
10	URBANLAB	ss3650663639	Oct 12, 2018 (152)
11	EVA_DECODE	ss3700541631	Jul 13, 2019 (153)
12	EVA_DECODE	ss3700541632	Jul 13, 2019 (153)
13	EVA_DECODE	ss3700541633	Jul 13, 2019 (153)
14	ACPOP	ss3742058315	Jul 13, 2019 (153)
15	ACPOP	ss3742058316	Jul 13, 2019 (153)
16	PACBIO	ss3788217696	Jul 13, 2019 (153)
17	PACBIO	ss3788217697	Jul 13, 2019 (153)
18	PACBIO	ss3793172799	Jul 13, 2019 (153)
19	PACBIO	ss3793172800	Jul 13, 2019 (153)
20	PACBIO	ss3798058560	Jul 13, 2019 (153)
21	PACBIO	ss3798058561	Jul 13, 2019 (153)
22	KHV_HUMAN_GENOMES	ss3819978001	Jul 13, 2019 (153)
23	EVA	ss3834886980	Apr 27, 2020 (154)
24	EVA	ss3841055637	Apr 27, 2020 (154)
25	EVA	ss3846552607	Apr 27, 2020 (154)
26	KOGIC	ss3978912361	Apr 27, 2020 (154)
27	KOGIC	ss3978912362	Apr 27, 2020 (154)
28	KOGIC	ss3978912363	Apr 27, 2020 (154)
29	GNOMAD	ss4312289758	Apr 27, 2021 (155)
30	GNOMAD	ss4312289759	Apr 27, 2021 (155)
31	GNOMAD	ss4312289760	Apr 27, 2021 (155)
32	GNOMAD	ss4312289761	Apr 27, 2021 (155)
33	GNOMAD	ss4312289762	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5222607284	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5222607285	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5222607286	Apr 27, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5303267065	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5303267066	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5303267067	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5496300711	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5496300712	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5778879112	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5778879113	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5778879114	Oct 16, 2022 (156)
45	EVA	ss5851820910	Oct 16, 2022 (156)
46	1000Genomes	NC_000017.10 - 46372983	Oct 12, 2018 (152)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508368296 (NC_000017.11:48295620::T 11116/130780) Row 508368297 (NC_000017.11:48295620::TT 122/130904) Row 508368298 (NC_000017.11:48295620::TTTT 1/130912)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508368296 (NC_000017.11:48295620::T 11116/130780) Row 508368297 (NC_000017.11:48295620::TT 122/130904) Row 508368298 (NC_000017.11:48295620::TTTT 1/130912)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508368296 (NC_000017.11:48295620::T 11116/130780) Row 508368297 (NC_000017.11:48295620::TT 122/130904) Row 508368298 (NC_000017.11:48295620::TTTT 1/130912)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508368296 (NC_000017.11:48295620::T 11116/130780) Row 508368297 (NC_000017.11:48295620::TT 122/130904) Row 508368298 (NC_000017.11:48295620::TTTT 1/130912)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 508368296 (NC_000017.11:48295620::T 11116/130780) Row 508368297 (NC_000017.11:48295620::TT 122/130904) Row 508368298 (NC_000017.11:48295620::TTTT 1/130912)...	-	Apr 27, 2021 (155)
52	Korean Genome Project Submission ignored due to conflicting rows: Row 35290362 (NC_000017.11:48295620:T: 53/1832) Row 35290363 (NC_000017.11:48295621::T 322/1832) Row 35290364 (NC_000017.11:48295621::TT 61/1832)	-	Apr 27, 2020 (154)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 35290362 (NC_000017.11:48295620:T: 53/1832) Row 35290363 (NC_000017.11:48295621::T 322/1832) Row 35290364 (NC_000017.11:48295621::TT 61/1832)	-	Apr 27, 2020 (154)
54	Korean Genome Project Submission ignored due to conflicting rows: Row 35290362 (NC_000017.11:48295620:T: 53/1832) Row 35290363 (NC_000017.11:48295621::T 322/1832) Row 35290364 (NC_000017.11:48295621::TT 61/1832)	-	Apr 27, 2020 (154)
55	Northern Sweden Submission ignored due to conflicting rows: Row 15343180 (NC_000017.10:46372982::T 60/598) Row 15343181 (NC_000017.10:46372982:T: 18/598)	-	Jul 13, 2019 (153)
56	Northern Sweden Submission ignored due to conflicting rows: Row 15343180 (NC_000017.10:46372982::T 60/598) Row 15343181 (NC_000017.10:46372982:T: 18/598)	-	Jul 13, 2019 (153)
57	8.3KJPN Submission ignored due to conflicting rows: Row 80576591 (NC_000017.10:46372982::T 3221/16754) Row 80576592 (NC_000017.10:46372982:T: 63/16754) Row 80576593 (NC_000017.10:46372982::TT 283/16754)	-	Apr 27, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 80576591 (NC_000017.10:46372982::T 3221/16754) Row 80576592 (NC_000017.10:46372982:T: 63/16754) Row 80576593 (NC_000017.10:46372982::TT 283/16754)	-	Apr 27, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 80576591 (NC_000017.10:46372982::T 3221/16754) Row 80576592 (NC_000017.10:46372982:T: 63/16754) Row 80576593 (NC_000017.10:46372982::TT 283/16754)	-	Apr 27, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 112716216 (NC_000017.11:48295620::T 5463/28256) Row 112716217 (NC_000017.11:48295620:T: 96/28256) Row 112716218 (NC_000017.11:48295620::TT 465/28256)	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 112716216 (NC_000017.11:48295620::T 5463/28256) Row 112716217 (NC_000017.11:48295620:T: 96/28256) Row 112716218 (NC_000017.11:48295620::TT 465/28256)	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 112716216 (NC_000017.11:48295620::T 5463/28256) Row 112716217 (NC_000017.11:48295620:T: 96/28256) Row 112716218 (NC_000017.11:48295620::TT 465/28256)	-	Oct 16, 2022 (156)
63	ALFA	NC_000017.11 - 48295621	Apr 27, 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)
rs374837873	May 15, 2013 (138)
rs66503049	May 11, 2012 (137)
rs71366855	May 11, 2012 (137)
rs397804320	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3700541631, ss4312289762	NC_000017.11:48295620:TT:	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4599191552	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss294915349	NC_000017.9:43727994:T:	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
72046056, ss1376692779, ss3015601246, ss3742058316, ss3788217696, ss3793172799, ss3798058560, ss3834886980, ss5222607285	NC_000017.10:46372982:T:	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3064712992, ss3650663639, ss3819978001, ss3978912361, ss4312289761, ss5303267066, ss5496300711, ss5778879113	NC_000017.11:48295620:T:	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4599191552	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3700541632	NC_000017.11:48295621:T:	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss96568505	NT_010783.15:11647134:T:	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss40800472, ss95695265	NT_010783.15:11647147:T:	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss289328042	NC_000017.9:43727995::T	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss664360466, ss3742058315, ss3788217697, ss3793172800, ss3798058561, ss3841055637, ss5222607284	NC_000017.10:46372982::T	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3846552607, ss4312289758, ss5303267065, ss5496300712, ss5778879112, ss5851820910	NC_000017.11:48295620::T	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4599191552	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3978912362	NC_000017.11:48295621::T	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3700541633	NC_000017.11:48295622::T	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5222607286	NC_000017.10:46372982::TT	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4312289759, ss5303267067, ss5778879114	NC_000017.11:48295620::TT	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4599191552	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3978912363	NC_000017.11:48295621::TT	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4312289760	NC_000017.11:48295620::TTTT	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4599191552	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000017.11:48295620:TTTTTTTTTTTT… NC_000017.11:48295620:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(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 rs35808845

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

rs35808845