RGD:8581042 Rat Genome Database

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Variant: RGD:8581042 -  Homo sapiens

RGD ID: 8581042
ClinVar ID: CV115479
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HCN1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 45,423,151
GRCh38 5 45,423,049
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000005.10:g.45423049T>G
NC_000005.9:g.45423151T>G
NM_021072.3:c.1012-26339A>C
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:HCN1
Accession:NM_021072
Location:INTRON

Variant Samples