RGD:8576736 Rat Genome Database

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Variant: RGD:8576736 -  Homo sapiens

RGD ID: 8576736
ClinVar ID: CV111104
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GRB14  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 165,405,108
GRCh38 2 164,548,598
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000002.12:g.164548598A>T
NC_000002.11:g.165405108A>T
NM_004490.2:c.325-782T>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:GRB14
Accession:NM_001303422
Location:INTRON

Gene Symbol:GRB14
Accession:XM_047444013
Location:INTRON

Gene Symbol:GRB14
Accession:XM_047444014
Location:INTRON

Gene Symbol:GRB14
Accession:XM_011511022
Location:INTRON

Gene Symbol:GRB14
Accession:NM_004490
Location:INTRON

Gene Symbol:GRB14
Accession:XR_427085
Location:INTRON;NON-CODING

Variant Samples