RGD:150462354 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: RGD:150462354 -  Homo sapiens

RGD ID: 150462354
RS ID: rs183124096
ClinVar ID: CV1253361
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FAR1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 13,729,639
GRCh38 11 13,708,092
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032228.6:c.545+13G>A
NG_041826.1:g.44434G>A
NC_000011.10:g.13708092G>A
NC_000011.9:g.13729639G>A
11/11/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FAR1
Accession:NM_032228
Location:INTRON

Gene Symbol:FAR1
Accession:XM_011520400
Location:INTRON

Gene Symbol:FAR1
Accession:XM_047427690
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001669690 CLINVAR
dbSNP (RS) rs183124096 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FAR1 CLINVAR
OMIM 616107 CLINVAR