RGD:150532430 Rat Genome Database

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Variant: RGD:150532430 -  Homo sapiens

RGD ID: 150532430
RS ID: rs139593793
ClinVar ID: CV1309189
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NFS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 34,268,992
GRCh38 20 35,681,070
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001198989.2:c.503-199C>T
NC_000020.11:g.35681070G>A
NM_021100.5:c.656-199C>T
NG_033237.1:g.23296C>T
More... 		07/09/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NFS1
Accession:NM_001198989
Location:INTRON

Gene Symbol:NFS1
Accession:NM_021100
Location:INTRON

Gene Symbol:NFS1
Accession:NR_037570
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001752870 CLINVAR
dbSNP (RS) rs139593793 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NFS1 CLINVAR
OMIM 603485 CLINVAR