RGD:150541646 Rat Genome Database

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Variant: RGD:150541646 -  Homo sapiens

RGD ID: 150541646
RS ID: rs34621588
ClinVar ID: CV1306485
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NFS1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 34,260,921
GRCh38 20 35,672,999
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000020.10:g.34260921A>G
NM_001198989.2:c.1068-155T>C
NM_021100.5:c.1221-155T>C
NG_033237.1:g.31367T>C
More...
07/31/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NFS1
Accession:NM_021100
Location:INTRON

Gene Symbol:NFS1
Accession:NM_001198989
Location:INTRON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001768107 CLINVAR
dbSNP (RS) rs34621588 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NFS1 CLINVAR
OMIM 603485 CLINVAR