rs752173466 Rat Genome Database

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Variant: rs752173466 -  Homo sapiens

RGD ID: 11627306
RS ID: rs752173466
ClinVar ID: CV349341
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRKCG  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 54,385,516
GRCh38 19 53,882,262
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_669:g.5050C>T
NG_009114.1:g.5050C>T
NC_000019.10:g.53882262C>T
NC_000019.9:g.54385516C>T
More... 		01/12/2018 5 prime utr variant uncertain significance Spinocerebellar Ataxia Type14
Disease Annotations     Click to see Annotation Detail View


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 RCV000279458 CLINVAR
dbSNP (RS) rs752173466 CLINVAR
MedGen C1854369 CLINVAR
NCBI Gene PRKCG CLINVAR
OMIM 176980 CLINVAR
  605361 CLINVAR