RGD:156198697 Rat Genome Database

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Variant: RGD:156198697 -  Homo sapiens

RGD ID: 156198697
ClinVar ID: CV2014632
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC129388668  PLA2G4A  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 186,919,871
GRCh38 1 186,950,739
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_596t1:c.1336+11C>T
NM_001311193.2:c.1156+11C>T
NM_024420.3:c.1336+11C>T
LRG_596:g.126840C>T
More... 		02/11/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PLA2G4A
Accession:XM_011509642
Location:INTRON

Gene Symbol:PLA2G4A
Accession:XM_005245267
Location:INTRON

Gene Symbol:PLA2G4A
Accession:NM_001311193
Location:INTRON

Gene Symbol:PLA2G4A
Accession:XM_047422599
Location:INTRON

Gene Symbol:PLA2G4A
Accession:NM_024420
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002700203 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC129388668 CLINVAR
  PLA2G4A CLINVAR
OMIM 600522 CLINVAR