RGD:405151379 Rat Genome Database

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Variant: RGD:405151379 -  Homo sapiens

RGD ID: 405151379
ClinVar ID: CV3031331
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PNLIP  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 118,306,798
GRCh38 10 116,547,286
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000936.4:c.47-8G>C
NG_023311.2:g.6357G>C
NG_023311.1:g.6371G>C
NC_000010.11:g.116547286G>C
More... 		04/27/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PNLIP
Accession:NM_000936
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003703276 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PNLIP CLINVAR
OMIM 246600 CLINVAR