RGD:401929172 Rat Genome Database

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Variant: RGD:401929172 -  Homo sapiens

RGD ID: 401929172
ClinVar ID: CV2818740
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRKCG  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 54,410,581
GRCh38 19 53,907,327
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_669t1:c.*432G>A
NM_001316329.2:c.*291G>A
NM_002739.5:c.*432G>A
LRG_669:g.30115G>A
More... 		05/01/2022 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PRKCG
Accession:NM_002739
Location:3UTRS;EXON

Gene Symbol:PRKCG
Accession:XM_047439092
Location:3UTRS;EXON

Gene Symbol:PRKCG
Accession:NM_001316329
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003407101 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PRKCG CLINVAR
OMIM 176980 CLINVAR