RGD:8583400 Rat Genome Database

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Variant: RGD:8583400 -  Homo sapiens

RGD ID: 8583400
ClinVar ID: CV117961
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ABCC4  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 13 95,849,477
GRCh38 13 95,197,223
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000013.11:g.95197223C>A
NC_000013.10:g.95849477C>A
NM_001105515.2:c.1162-2286G>T
NM_001105515.1:c.1162-2286G>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ABCC4
Accession:NM_001301829
Location:INTRON

Gene Symbol:ABCC4
Accession:NM_001105515
Location:INTRON

Gene Symbol:ABCC4
Accession:NM_005845
Location:INTRON

Gene Symbol:ABCC4
Accession:XM_047430035
Location:INTRON

Gene Symbol:ABCC4
Accession:XM_047430034
Location:INTRON

Gene Symbol:ABCC4
Accession:NM_001301830
Location:INTRON

Gene Symbol:ABCC4
Accession:XM_017020320
Location:INTRON

Variant Samples