RGD:11659623 Rat Genome Database

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Variant: RGD:11659623 -  Homo sapiens

RGD ID: 11659623
ClinVar ID: CV311039
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: STXBP1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 130,453,978
GRCh38 9 127,691,699
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_016623.1:g.84493G>T
NC_000009.12:g.127691699G>T
NC_000009.11:g.130453978G>T
NM_001032221.4:c.*842G>T
More... 		06/14/2016 3 prime utr variant uncertain significance

Variant Details
Variant Transcripts
Gene Symbol:STXBP1
Accession:NM_003165
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001374311
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001374310
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001374313
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001374309
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001032221
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001374312
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001374307
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001374315
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001374308
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001374306
Location:3UTRS;EXON

Gene Symbol:STXBP1
Accession:NM_001374314
Location:INTRON

Variant Samples