RGD:21069779 Rat Genome Database

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Variant: RGD:21069779 -  Homo sapiens

RGD ID: 21069779
RS ID: rs374622415
ClinVar ID: CV796182
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CA8  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 61,144,837
GRCh38 8 60,232,278
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001321839.2:c.418-5343C>T
NM_001321837.2:c.513+6C>T
NG_023193.2:g.54118C>T
NC_000008.11:g.60232278G>A
More...
05/01/2016 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:CA8
Accession:NM_004056
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:CA8
Accession:NM_001321839
Location:INTRON

Gene Symbol:CA8
Accession:NM_001321837
Location:INTRON

Gene Symbol:CA8
Accession:NM_001321838
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:CA8
Accession:NR_135821
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000999038 CLINVAR
dbSNP (RS) rs374622415 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CA8 CLINVAR
OMIM 114815 CLINVAR