RGD:8586410 Rat Genome Database

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Variant: RGD:8586410 -  Homo sapiens

RGD ID: 8586410
ClinVar ID: CV121012
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HCK  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 30,673,760
GRCh38 20 32,085,957
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001172133.1:c.773-671C>A
NG_029471.1:g.38770C>A
NC_000020.11:g.32085957C>A
NC_000020.10:g.30673760C>A
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:HCK
Accession:NM_001172132
Location:INTRON

Gene Symbol:HCK
Accession:NM_001172133
Location:INTRON

Gene Symbol:HCK
Accession:NM_002110
Location:INTRON

Gene Symbol:HCK
Accession:NM_001172129
Location:INTRON

Gene Symbol:HCK
Accession:NM_001172130
Location:INTRON

Gene Symbol:HCK
Accession:NM_001172131
Location:INTRON

Variant Samples