RGD:8584607 Rat Genome Database

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Variant: RGD:8584607 -  Homo sapiens

RGD ID: 8584607
ClinVar ID: CV119183
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AKAP13  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 86,257,740
GRCh38 15 85,714,509
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000015.10:g.85714509G>C
NC_000015.9:g.86257740G>C
NM_001270546.1:c.1463-1279G>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:AKAP13
Accession:NM_006738
Location:INTRON

Gene Symbol:AKAP13
Accession:NM_001270546
Location:INTRON

Gene Symbol:AKAP13
Accession:NM_007200
Location:INTRON

Variant Samples