RGD:14719171 Rat Genome Database

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Variant: RGD:14719171 -  Homo sapiens

RGD ID: 14719171
RS ID: rs17336615
ClinVar ID: CV670240
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NFS1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 20 34,262,011
GRCh38 20 35,674,089
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021100.5:c.1136+261T>G
NM_001198989.2:c.983+261T>G
NG_033237.1:g.30277T>G
NC_000020.11:g.35674089A>C
More... 		06/16/2018 intron variant 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 RCV000830655 CLINVAR
dbSNP (RS) rs17336615 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NFS1 CLINVAR
OMIM 603485 CLINVAR