RGD:404986444 Rat Genome Database

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Variant: RGD:404986444 -  Homo sapiens

RGD ID: 404986444
ClinVar ID: CV2852308
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRKCG  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 54,385,737
GRCh38 19 53,882,483
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_669t1:c.-12G>T
NM_001316329.2:c.-12G>T
NM_002739.5:c.-12G>T
LRG_669:g.5271G>T
More... 		12/15/2023 5 prime utr variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:PRKCG
Accession:NM_002739
Location:5UTRS;EXON

Gene Symbol:PRKCG
Accession:NM_001316329
Location:5UTRS;EXON

Gene Symbol:PRKCG
Accession:XM_047439092
Location:5UTRS;INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003489558 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene PRKCG CLINVAR
OMIM 176980 CLINVAR