RGD:150543418 Rat Genome Database

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Variant: RGD:150543418 -  Homo sapiens

RGD ID: 150543418
RS ID: rs17092960
ClinVar ID: CV1308971
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NFS1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 20 34,257,297
GRCh38 20 35,669,375
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.34257297T>C
NR_037570.3:n.1807A>G
NM_001198989.2:c.*247A>G
NC_000020.11:g.35669375T>C
More...
07/17/2019 3 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NFS1
Accession:NM_021100
Location:3UTRS;EXON

Gene Symbol:NFS1
Accession:NM_001198989
Location:3UTRS;EXON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001769884 CLINVAR
dbSNP (RS) rs17092960 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NFS1 CLINVAR
OMIM 603485 CLINVAR