RGD:14717687 Rat Genome Database

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Variant: RGD:14717687 -  Homo sapiens

RGD ID: 14717687
ClinVar ID: CV671387
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL5A1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 137,622,039
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000009.11:g.137622039G>A
NM_000093.3:c.925-43G>A
NC_000009.12:g.134730193G>A
06/14/2018 benign

Variant Details
Variant Transcripts
Gene Symbol:COL5A1
Accession:NM_001278074
Location:INTRON

Gene Symbol:COL5A1
Accession:NM_000093
Location:INTRON

Variant Samples