Name: rs59276192
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.

rs59276192

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:15318531-15318548 (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)₉ / del(A)₈ / del(A)₆ / del(…
del(A)₉ / del(A)₈ / del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₈=0.000004 (1/264690, TOPMED)
dupA=0.2548 (1276/5008, 1000G)
del(A)₉=0.0000 (0/3990, ALFA) (+ 8 more)
del(A)₈=0.0000 (0/3990, ALFA)
del(A)₆=0.0000 (0/3990, ALFA)
delAAA=0.0000 (0/3990, ALFA)
delAA=0.0000 (0/3990, ALFA)
delA=0.0000 (0/3990, ALFA)
dupA=0.0000 (0/3990, ALFA)
dupAA=0.0000 (0/3990, ALFA)
dupAAA=0.0000 (0/3990, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SH3BP5 : 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	HWEP
Total	Global	3990	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2762	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	720	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	18	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	702	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	42	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	26	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	16	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	36	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	244	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	32	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	154	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	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
TopMed	Global	Study-wide	264690	(A)₁₈=0.999996	del(A)₈=0.000004
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.2548
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.2549
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.2431
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.3161
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.232
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.215
Allele Frequency Aggregator	Total	Global	3990	(A)₁₈=1.0000	del(A)₉=0.0000, del(A)₈=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	2762	(A)₁₈=1.0000	del(A)₉=0.0000, del(A)₈=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	720	(A)₁₈=1.000	del(A)₉=0.000, del(A)₈=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	244	(A)₁₈=1.000	del(A)₉=0.000, del(A)₈=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	154	(A)₁₈=1.000	del(A)₉=0.000, del(A)₈=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Asian	Sub	42	(A)₁₈=1.00	del(A)₉=0.00, del(A)₈=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	36	(A)₁₈=1.00	del(A)₉=0.00, del(A)₈=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(A)₁₈=1.00	del(A)₉=0.00, del(A)₈=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=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 3	NC_000003.12:g.15318540_15318548del
GRCh38.p14 chr 3	NC_000003.12:g.15318541_15318548del
GRCh38.p14 chr 3	NC_000003.12:g.15318543_15318548del
GRCh38.p14 chr 3	NC_000003.12:g.15318545_15318548del
GRCh38.p14 chr 3	NC_000003.12:g.15318546_15318548del
GRCh38.p14 chr 3	NC_000003.12:g.15318547_15318548del
GRCh38.p14 chr 3	NC_000003.12:g.15318548del
GRCh38.p14 chr 3	NC_000003.12:g.15318548dup
GRCh38.p14 chr 3	NC_000003.12:g.15318547_15318548dup
GRCh38.p14 chr 3	NC_000003.12:g.15318546_15318548dup
GRCh38.p14 chr 3	NC_000003.12:g.15318545_15318548dup
GRCh38.p14 chr 3	NC_000003.12:g.15318544_15318548dup
GRCh37.p13 chr 3	NC_000003.11:g.15360047_15360055del
GRCh37.p13 chr 3	NC_000003.11:g.15360048_15360055del
GRCh37.p13 chr 3	NC_000003.11:g.15360050_15360055del
GRCh37.p13 chr 3	NC_000003.11:g.15360052_15360055del
GRCh37.p13 chr 3	NC_000003.11:g.15360053_15360055del
GRCh37.p13 chr 3	NC_000003.11:g.15360054_15360055del
GRCh37.p13 chr 3	NC_000003.11:g.15360055del
GRCh37.p13 chr 3	NC_000003.11:g.15360055dup
GRCh37.p13 chr 3	NC_000003.11:g.15360054_15360055dup
GRCh37.p13 chr 3	NC_000003.11:g.15360053_15360055dup
GRCh37.p13 chr 3	NC_000003.11:g.15360052_15360055dup
GRCh37.p13 chr 3	NC_000003.11:g.15360051_15360055dup

Gene: SH3BP5, SH3 domain binding protein 5 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SH3BP5 transcript variant 2	NM_001018009.4:c.-339+119… NM_001018009.4:c.-339+11965_-339+11973del	N/A	Intron Variant
SH3BP5 transcript variant 1	NM_004844.5:c.201+11965_2… NM_004844.5:c.201+11965_201+11973del	N/A	Intron Variant
SH3BP5 transcript variant X2	XM_011534251.3:c.81+11965… XM_011534251.3:c.81+11965_81+11973del	N/A	Intron Variant
SH3BP5 transcript variant X5	XM_017007525.2:c.180+1196… XM_017007525.2:c.180+11965_180+11973del	N/A	Intron Variant
SH3BP5 transcript variant X1	XM_047449240.1:c.162+1196… XM_047449240.1:c.162+11965_162+11973del	N/A	Intron Variant
SH3BP5 transcript variant X3	XM_047449241.1:c.201+1196… XM_047449241.1:c.201+11965_201+11973del	N/A	Intron Variant
SH3BP5 transcript variant X4	XM_047449242.1:c.81+11965… XM_047449242.1:c.81+11965_81+11973del	N/A	Intron Variant
SH3BP5 transcript variant X6	XM_047449244.1:c.	N/A	Genic Upstream Transcript Variant
SH3BP5 transcript variant X7	XM_047449245.1: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	(A)₁₈=	del(A)₉	del(A)₈	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅
GRCh38.p14 chr 3	NC_000003.12:g.15318531_15318548=	NC_000003.12:g.15318540_15318548del	NC_000003.12:g.15318541_15318548del	NC_000003.12:g.15318543_15318548del	NC_000003.12:g.15318545_15318548del	NC_000003.12:g.15318546_15318548del	NC_000003.12:g.15318547_15318548del	NC_000003.12:g.15318548del	NC_000003.12:g.15318548dup	NC_000003.12:g.15318547_15318548dup	NC_000003.12:g.15318546_15318548dup	NC_000003.12:g.15318545_15318548dup	NC_000003.12:g.15318544_15318548dup
GRCh37.p13 chr 3	NC_000003.11:g.15360038_15360055=	NC_000003.11:g.15360047_15360055del	NC_000003.11:g.15360048_15360055del	NC_000003.11:g.15360050_15360055del	NC_000003.11:g.15360052_15360055del	NC_000003.11:g.15360053_15360055del	NC_000003.11:g.15360054_15360055del	NC_000003.11:g.15360055del	NC_000003.11:g.15360055dup	NC_000003.11:g.15360054_15360055dup	NC_000003.11:g.15360053_15360055dup	NC_000003.11:g.15360052_15360055dup	NC_000003.11:g.15360051_15360055dup
SH3BP5 transcript variant 2	NM_001018009.3:c.-339+11973=	NM_001018009.3:c.-339+11965_-339+11973del	NM_001018009.3:c.-339+11966_-339+11973del	NM_001018009.3:c.-339+11968_-339+11973del	NM_001018009.3:c.-339+11970_-339+11973del	NM_001018009.3:c.-339+11971_-339+11973del	NM_001018009.3:c.-339+11972_-339+11973del	NM_001018009.3:c.-339+11973del	NM_001018009.3:c.-339+11973dup	NM_001018009.3:c.-339+11972_-339+11973dup	NM_001018009.3:c.-339+11971_-339+11973dup	NM_001018009.3:c.-339+11970_-339+11973dup	NM_001018009.3:c.-339+11969_-339+11973dup
SH3BP5 transcript variant 2	NM_001018009.4:c.-339+11973=	NM_001018009.4:c.-339+11965_-339+11973del	NM_001018009.4:c.-339+11966_-339+11973del	NM_001018009.4:c.-339+11968_-339+11973del	NM_001018009.4:c.-339+11970_-339+11973del	NM_001018009.4:c.-339+11971_-339+11973del	NM_001018009.4:c.-339+11972_-339+11973del	NM_001018009.4:c.-339+11973del	NM_001018009.4:c.-339+11973dup	NM_001018009.4:c.-339+11972_-339+11973dup	NM_001018009.4:c.-339+11971_-339+11973dup	NM_001018009.4:c.-339+11970_-339+11973dup	NM_001018009.4:c.-339+11969_-339+11973dup
SH3BP5 transcript variant 1	NM_004844.4:c.201+11973=	NM_004844.4:c.201+11965_201+11973del	NM_004844.4:c.201+11966_201+11973del	NM_004844.4:c.201+11968_201+11973del	NM_004844.4:c.201+11970_201+11973del	NM_004844.4:c.201+11971_201+11973del	NM_004844.4:c.201+11972_201+11973del	NM_004844.4:c.201+11973del	NM_004844.4:c.201+11973dup	NM_004844.4:c.201+11972_201+11973dup	NM_004844.4:c.201+11971_201+11973dup	NM_004844.4:c.201+11970_201+11973dup	NM_004844.4:c.201+11969_201+11973dup
SH3BP5 transcript variant 1	NM_004844.5:c.201+11973=	NM_004844.5:c.201+11965_201+11973del	NM_004844.5:c.201+11966_201+11973del	NM_004844.5:c.201+11968_201+11973del	NM_004844.5:c.201+11970_201+11973del	NM_004844.5:c.201+11971_201+11973del	NM_004844.5:c.201+11972_201+11973del	NM_004844.5:c.201+11973del	NM_004844.5:c.201+11973dup	NM_004844.5:c.201+11972_201+11973dup	NM_004844.5:c.201+11971_201+11973dup	NM_004844.5:c.201+11970_201+11973dup	NM_004844.5:c.201+11969_201+11973dup
SH3BP5 transcript variant X1	XM_005265588.1:c.162+11973=	XM_005265588.1:c.162+11965_162+11973del	XM_005265588.1:c.162+11966_162+11973del	XM_005265588.1:c.162+11968_162+11973del	XM_005265588.1:c.162+11970_162+11973del	XM_005265588.1:c.162+11971_162+11973del	XM_005265588.1:c.162+11972_162+11973del	XM_005265588.1:c.162+11973del	XM_005265588.1:c.162+11973dup	XM_005265588.1:c.162+11972_162+11973dup	XM_005265588.1:c.162+11971_162+11973dup	XM_005265588.1:c.162+11970_162+11973dup	XM_005265588.1:c.162+11969_162+11973dup
SH3BP5 transcript variant X2	XM_005265589.1:c.81+11973=	XM_005265589.1:c.81+11965_81+11973del	XM_005265589.1:c.81+11966_81+11973del	XM_005265589.1:c.81+11968_81+11973del	XM_005265589.1:c.81+11970_81+11973del	XM_005265589.1:c.81+11971_81+11973del	XM_005265589.1:c.81+11972_81+11973del	XM_005265589.1:c.81+11973del	XM_005265589.1:c.81+11973dup	XM_005265589.1:c.81+11972_81+11973dup	XM_005265589.1:c.81+11971_81+11973dup	XM_005265589.1:c.81+11970_81+11973dup	XM_005265589.1:c.81+11969_81+11973dup
SH3BP5 transcript variant X3	XM_005265590.1:c.78+11973=	XM_005265590.1:c.78+11965_78+11973del	XM_005265590.1:c.78+11966_78+11973del	XM_005265590.1:c.78+11968_78+11973del	XM_005265590.1:c.78+11970_78+11973del	XM_005265590.1:c.78+11971_78+11973del	XM_005265590.1:c.78+11972_78+11973del	XM_005265590.1:c.78+11973del	XM_005265590.1:c.78+11973dup	XM_005265590.1:c.78+11972_78+11973dup	XM_005265590.1:c.78+11971_78+11973dup	XM_005265590.1:c.78+11970_78+11973dup	XM_005265590.1:c.78+11969_78+11973dup
SH3BP5 transcript variant X4	XM_005265591.1:c.-561+11973=	XM_005265591.1:c.-561+11965_-561+11973del	XM_005265591.1:c.-561+11966_-561+11973del	XM_005265591.1:c.-561+11968_-561+11973del	XM_005265591.1:c.-561+11970_-561+11973del	XM_005265591.1:c.-561+11971_-561+11973del	XM_005265591.1:c.-561+11972_-561+11973del	XM_005265591.1:c.-561+11973del	XM_005265591.1:c.-561+11973dup	XM_005265591.1:c.-561+11972_-561+11973dup	XM_005265591.1:c.-561+11971_-561+11973dup	XM_005265591.1:c.-561+11970_-561+11973dup	XM_005265591.1:c.-561+11969_-561+11973dup
SH3BP5 transcript variant X2	XM_011534251.3:c.81+11973=	XM_011534251.3:c.81+11965_81+11973del	XM_011534251.3:c.81+11966_81+11973del	XM_011534251.3:c.81+11968_81+11973del	XM_011534251.3:c.81+11970_81+11973del	XM_011534251.3:c.81+11971_81+11973del	XM_011534251.3:c.81+11972_81+11973del	XM_011534251.3:c.81+11973del	XM_011534251.3:c.81+11973dup	XM_011534251.3:c.81+11972_81+11973dup	XM_011534251.3:c.81+11971_81+11973dup	XM_011534251.3:c.81+11970_81+11973dup	XM_011534251.3:c.81+11969_81+11973dup
SH3BP5 transcript variant X5	XM_017007525.2:c.180+11973=	XM_017007525.2:c.180+11965_180+11973del	XM_017007525.2:c.180+11966_180+11973del	XM_017007525.2:c.180+11968_180+11973del	XM_017007525.2:c.180+11970_180+11973del	XM_017007525.2:c.180+11971_180+11973del	XM_017007525.2:c.180+11972_180+11973del	XM_017007525.2:c.180+11973del	XM_017007525.2:c.180+11973dup	XM_017007525.2:c.180+11972_180+11973dup	XM_017007525.2:c.180+11971_180+11973dup	XM_017007525.2:c.180+11970_180+11973dup	XM_017007525.2:c.180+11969_180+11973dup
SH3BP5 transcript variant X1	XM_047449240.1:c.162+11973=	XM_047449240.1:c.162+11965_162+11973del	XM_047449240.1:c.162+11966_162+11973del	XM_047449240.1:c.162+11968_162+11973del	XM_047449240.1:c.162+11970_162+11973del	XM_047449240.1:c.162+11971_162+11973del	XM_047449240.1:c.162+11972_162+11973del	XM_047449240.1:c.162+11973del	XM_047449240.1:c.162+11973dup	XM_047449240.1:c.162+11972_162+11973dup	XM_047449240.1:c.162+11971_162+11973dup	XM_047449240.1:c.162+11970_162+11973dup	XM_047449240.1:c.162+11969_162+11973dup
SH3BP5 transcript variant X3	XM_047449241.1:c.201+11973=	XM_047449241.1:c.201+11965_201+11973del	XM_047449241.1:c.201+11966_201+11973del	XM_047449241.1:c.201+11968_201+11973del	XM_047449241.1:c.201+11970_201+11973del	XM_047449241.1:c.201+11971_201+11973del	XM_047449241.1:c.201+11972_201+11973del	XM_047449241.1:c.201+11973del	XM_047449241.1:c.201+11973dup	XM_047449241.1:c.201+11972_201+11973dup	XM_047449241.1:c.201+11971_201+11973dup	XM_047449241.1:c.201+11970_201+11973dup	XM_047449241.1:c.201+11969_201+11973dup
SH3BP5 transcript variant X4	XM_047449242.1:c.81+11973=	XM_047449242.1:c.81+11965_81+11973del	XM_047449242.1:c.81+11966_81+11973del	XM_047449242.1:c.81+11968_81+11973del	XM_047449242.1:c.81+11970_81+11973del	XM_047449242.1:c.81+11971_81+11973del	XM_047449242.1:c.81+11972_81+11973del	XM_047449242.1:c.81+11973del	XM_047449242.1:c.81+11973dup	XM_047449242.1:c.81+11972_81+11973dup	XM_047449242.1:c.81+11971_81+11973dup	XM_047449242.1:c.81+11970_81+11973dup	XM_047449242.1:c.81+11969_81+11973dup

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, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79890562	Dec 04, 2013 (142)
2	HGSV	ss81116688	Dec 03, 2013 (142)
3	HGSV	ss81478556	Dec 04, 2013 (142)
4	HGSV	ss82262763	Dec 04, 2013 (142)
5	HGSV	ss82266923	Dec 04, 2013 (142)
6	PJP	ss295089327	May 09, 2011 (134)
7	PJP	ss295089328	May 09, 2011 (134)
8	BILGI_BIOE	ss666198023	Apr 25, 2013 (138)
9	1000GENOMES	ss1370019076	Aug 21, 2014 (142)
10	SWEGEN	ss2991878031	Nov 08, 2017 (151)
11	EVA_DECODE	ss3708697122	Jul 13, 2019 (153)
12	EVA_DECODE	ss3708697123	Jul 13, 2019 (153)
13	EVA_DECODE	ss3708697124	Jul 13, 2019 (153)
14	EVA_DECODE	ss3708697125	Jul 13, 2019 (153)
15	EVA_DECODE	ss3708697126	Jul 13, 2019 (153)
16	EVA_DECODE	ss3708697127	Jul 13, 2019 (153)
17	PACBIO	ss3789770820	Jul 13, 2019 (153)
18	PACBIO	ss3794644573	Jul 13, 2019 (153)
19	KHV_HUMAN_GENOMES	ss3802848198	Jul 13, 2019 (153)
20	EVA	ss3827676723	Apr 25, 2020 (154)
21	KOGIC	ss3950727634	Apr 25, 2020 (154)
22	KOGIC	ss3950727635	Apr 25, 2020 (154)
23	KOGIC	ss3950727636	Apr 25, 2020 (154)
24	KOGIC	ss3950727637	Apr 25, 2020 (154)
25	GNOMAD	ss4066349405	Apr 26, 2021 (155)
26	GNOMAD	ss4066349406	Apr 26, 2021 (155)
27	GNOMAD	ss4066349407	Apr 26, 2021 (155)
28	GNOMAD	ss4066349408	Apr 26, 2021 (155)
29	GNOMAD	ss4066349409	Apr 26, 2021 (155)
30	GNOMAD	ss4066349410	Apr 26, 2021 (155)
31	GNOMAD	ss4066349411	Apr 26, 2021 (155)
32	GNOMAD	ss4066349412	Apr 26, 2021 (155)
33	GNOMAD	ss4066349413	Apr 26, 2021 (155)
34	GNOMAD	ss4066349414	Apr 26, 2021 (155)
35	TOPMED	ss4555217916	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5157933555	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5157933556	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5157933557	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5157933558	Apr 26, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5253153261	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5253153262	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5253153263	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5452642802	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5452642803	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5452642804	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5452642805	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5689240949	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5689240950	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5689240951	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5689240953	Oct 13, 2022 (156)
51	EVA	ss5825387194	Oct 13, 2022 (156)
52	EVA	ss5825387195	Oct 13, 2022 (156)
53	EVA	ss5853503678	Oct 13, 2022 (156)
54	1000Genomes	NC_000003.11 - 15360038	Oct 12, 2018 (152)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99883774 (NC_000003.12:15318530::A 39168/96694) Row 99883775 (NC_000003.12:15318530::AA 1957/96808) Row 99883776 (NC_000003.12:15318530::AAA 30/96928)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99883774 (NC_000003.12:15318530::A 39168/96694) Row 99883775 (NC_000003.12:15318530::AA 1957/96808) Row 99883776 (NC_000003.12:15318530::AAA 30/96928)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99883774 (NC_000003.12:15318530::A 39168/96694) Row 99883775 (NC_000003.12:15318530::AA 1957/96808) Row 99883776 (NC_000003.12:15318530::AAA 30/96928)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99883774 (NC_000003.12:15318530::A 39168/96694) Row 99883775 (NC_000003.12:15318530::AA 1957/96808) Row 99883776 (NC_000003.12:15318530::AAA 30/96928)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99883774 (NC_000003.12:15318530::A 39168/96694) Row 99883775 (NC_000003.12:15318530::AA 1957/96808) Row 99883776 (NC_000003.12:15318530::AAA 30/96928)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99883774 (NC_000003.12:15318530::A 39168/96694) Row 99883775 (NC_000003.12:15318530::AA 1957/96808) Row 99883776 (NC_000003.12:15318530::AAA 30/96928)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99883774 (NC_000003.12:15318530::A 39168/96694) Row 99883775 (NC_000003.12:15318530::AA 1957/96808) Row 99883776 (NC_000003.12:15318530::AAA 30/96928)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99883774 (NC_000003.12:15318530::A 39168/96694) Row 99883775 (NC_000003.12:15318530::AA 1957/96808) Row 99883776 (NC_000003.12:15318530::AAA 30/96928)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99883774 (NC_000003.12:15318530::A 39168/96694) Row 99883775 (NC_000003.12:15318530::AA 1957/96808) Row 99883776 (NC_000003.12:15318530::AAA 30/96928)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 99883774 (NC_000003.12:15318530::A 39168/96694) Row 99883775 (NC_000003.12:15318530::AA 1957/96808) Row 99883776 (NC_000003.12:15318530::AAA 30/96928)...	-	Apr 26, 2021 (155)
65	Korean Genome Project Submission ignored due to conflicting rows: Row 7105635 (NC_000003.12:15318532::A 530/1814) Row 7105636 (NC_000003.12:15318531:A: 209/1814) Row 7105637 (NC_000003.12:15318532::AA 48/1814)...	-	Apr 25, 2020 (154)
66	Korean Genome Project Submission ignored due to conflicting rows: Row 7105635 (NC_000003.12:15318532::A 530/1814) Row 7105636 (NC_000003.12:15318531:A: 209/1814) Row 7105637 (NC_000003.12:15318532::AA 48/1814)...	-	Apr 25, 2020 (154)
67	Korean Genome Project Submission ignored due to conflicting rows: Row 7105635 (NC_000003.12:15318532::A 530/1814) Row 7105636 (NC_000003.12:15318531:A: 209/1814) Row 7105637 (NC_000003.12:15318532::AA 48/1814)...	-	Apr 25, 2020 (154)
68	Korean Genome Project Submission ignored due to conflicting rows: Row 7105635 (NC_000003.12:15318532::A 530/1814) Row 7105636 (NC_000003.12:15318531:A: 209/1814) Row 7105637 (NC_000003.12:15318532::AA 48/1814)...	-	Apr 25, 2020 (154)
69	8.3KJPN Submission ignored due to conflicting rows: Row 15902862 (NC_000003.11:15360037::A 5783/16684) Row 15902863 (NC_000003.11:15360037:A: 51/16684) Row 15902864 (NC_000003.11:15360037::AA 238/16684)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 15902862 (NC_000003.11:15360037::A 5783/16684) Row 15902863 (NC_000003.11:15360037:A: 51/16684) Row 15902864 (NC_000003.11:15360037::AA 238/16684)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 15902862 (NC_000003.11:15360037::A 5783/16684) Row 15902863 (NC_000003.11:15360037:A: 51/16684) Row 15902864 (NC_000003.11:15360037::AA 238/16684)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 15902862 (NC_000003.11:15360037::A 5783/16684) Row 15902863 (NC_000003.11:15360037:A: 51/16684) Row 15902864 (NC_000003.11:15360037::AA 238/16684)...	-	Apr 26, 2021 (155)
73	14KJPN Submission ignored due to conflicting rows: Row 23078053 (NC_000003.12:15318530::A 10108/28254) Row 23078054 (NC_000003.12:15318530::AA 444/28254) Row 23078055 (NC_000003.12:15318530:A: 74/28254)...	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 23078053 (NC_000003.12:15318530::A 10108/28254) Row 23078054 (NC_000003.12:15318530::AA 444/28254) Row 23078055 (NC_000003.12:15318530:A: 74/28254)...	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 23078053 (NC_000003.12:15318530::A 10108/28254) Row 23078054 (NC_000003.12:15318530::AA 444/28254) Row 23078055 (NC_000003.12:15318530:A: 74/28254)...	-	Oct 13, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 23078053 (NC_000003.12:15318530::A 10108/28254) Row 23078054 (NC_000003.12:15318530::AA 444/28254) Row 23078055 (NC_000003.12:15318530:A: 74/28254)...	-	Oct 13, 2022 (156)
77	TopMed	NC_000003.12 - 15318531	Apr 26, 2021 (155)
78	ALFA	NC_000003.12 - 15318531	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)
rs397762192	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
2047635745	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
392595471, ss4555217916	NC_000003.12:15318530:AAAAAAAA:	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
2047635745	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4066349414	NC_000003.12:15318530:AAAAAA:	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
2047635745	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4066349413	NC_000003.12:15318530:AAAA:	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3708697127, ss4066349412	NC_000003.12:15318530:AAA:	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
2047635745	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3950727637, ss4066349411, ss5452642805	NC_000003.12:15318530:AA:	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
2047635745	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3708697126	NC_000003.12:15318531:AA:	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss2991878031, ss5157933556	NC_000003.11:15360037:A:	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4066349410, ss5253153261, ss5452642802, ss5689240951	NC_000003.12:15318530:A:	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
2047635745	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3950727635	NC_000003.12:15318531:A:	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3708697125	NC_000003.12:15318532:A:	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss295089327	NC_000003.10:15335042::A	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss295089328	NC_000003.10:15335059::A	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
14073422, ss666198023, ss1370019076, ss3789770820, ss3794644573, ss3827676723, ss5157933555, ss5825387194	NC_000003.11:15360037::A	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3802848198, ss4066349405, ss5253153262, ss5452642803, ss5689240949	NC_000003.12:15318530::A	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
2047635745	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3950727634	NC_000003.12:15318532::A	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3708697124	NC_000003.12:15318533::A	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss79890562, ss81116688, ss81478556, ss82262763, ss82266923	NT_022517.18:15300055::A	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5157933557, ss5825387195	NC_000003.11:15360037::AA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4066349406, ss5253153263, ss5452642804, ss5689240950, ss5853503678	NC_000003.12:15318530::AA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
2047635745	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3950727636	NC_000003.12:15318532::AA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3708697123	NC_000003.12:15318533::AA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5157933558	NC_000003.11:15360037::AAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4066349407, ss5689240953	NC_000003.12:15318530::AAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
2047635745	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4066349408	NC_000003.12:15318530::AAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4066349409	NC_000003.12:15318530::AAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3708697122	NC_000003.12:15318533::AAAAA	NC_000003.12:15318530:AAAAAAAAAAAA… NC_000003.12:15318530:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(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 rs59276192

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs59276192