RGD:150508705 Rat Genome Database

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Variant: RGD:150508705 -  Homo sapiens

RGD ID: 150508705
RS ID: rs2074354
ClinVar ID: CV1229711
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PON1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 94,940,587
GRCh38 7 95,311,275
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000446.7:c.497+176C>T
NG_008779.2:g.18432C>T
NC_000007.14:g.95311275G>A
NC_000007.13:g.94940587G>A
 06/20/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PON1
Accession:NM_000446
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001636289 CLINVAR
dbSNP (RS) rs2074354 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PON1 CLINVAR
OMIM 168820 CLINVAR