RGD:8650748 Rat Genome Database

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Variant: RGD:8650748 -  Homo sapiens

RGD ID: 8650748
ClinVar ID: CV127323
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CA13  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 86,186,623
GRCh38 8 85,274,394
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.85274394G>A
NC_000008.10:g.86186623G>A
NM_198584.2:c.669+5767G>A
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:CA13
Accession:NM_198584
Location:INTRON

Variant Samples