RGD:8587038 Rat Genome Database

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Variant: RGD:8587038 -  Homo sapiens

RGD ID: 8587038
ClinVar ID: CV121664
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRPC5  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 111,200,518
GRCh38 X 111,957,290
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_012471.2:c.-21-4849T>A
NG_021215.1:g.130487T>A
NC_000023.11:g.111957290A>T
NC_000023.10:g.111200518A>T
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:TRPC5
Accession:NM_012471
Location:5UTRS;INTRON

Gene Symbol:TRPC5
Accession:XM_017029774
Location:5UTRS;INTRON

Gene Symbol:TRPC5
Accession:XM_047442413
Location:5UTRS;INTRON

Variant Samples