RGD:8650600 Rat Genome Database

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Variant: RGD:8650600 -  Homo sapiens

RGD ID: 8650600
ClinVar ID: CV127175
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNB2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 73,705,714
GRCh38 8 72,793,479
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.11:g.72793479G>A
NC_000008.10:g.73705714G>A
NM_004770.2:c.580-142456G>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:KCNB2
Accession:NM_004770
Location:INTRON

Gene Symbol:KCNB2
Accession:XM_017013982
Location:INTRON

Variant Samples