RGD:150440533 Rat Genome Database

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Variant: RGD:150440533 -  Homo sapiens

RGD ID: 150440533
RS ID: rs5030772
ClinVar ID: CV1265123
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FASLG  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 172,633,350
GRCh38 1 172,664,210
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000639.3:c.395-124A>G
LRG_58:g.10166A>G
NG_007269.1:g.10166A>G
NC_000001.11:g.172664210A>G
More... 		11/08/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FASLG
Accession:NM_000639
Location:INTRON

Gene Symbol:FASLG
Accession:NM_001302746
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001679116 CLINVAR
dbSNP (RS) rs5030772 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FASLG CLINVAR
OMIM 134638 CLINVAR