RGD:405112048 Rat Genome Database

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Variant: RGD:405112048 -  Homo sapiens

RGD ID: 405112048
ClinVar ID: CV3137283
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LPL  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 19,816,903
GRCh38 8 19,959,392
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1298t1:c.1139+12A>T
NM_000237.3:c.1139+12A>T
LRG_1298:g.62676A>T
NG_008855.2:g.62676A>T
More... 		12/12/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LPL
Accession:NM_000237
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003836246 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LPL CLINVAR
OMIM 609708 CLINVAR