RGD:150457364 Rat Genome Database

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Variant: RGD:150457364 -  Homo sapiens

RGD ID: 150457364
RS ID: rs7202091
ClinVar ID: CV1278615
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCA  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 89,851,575
GRCh38 16 89,785,167
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000135.4:c.1360-203=
NM_001286167.3:c.1360-203=
LRG_495:g.36491C>T
NG_011706.1:g.36491C>T
More... 		04/09/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FANCA
Accession:NM_000135
Location:INTRON

Gene Symbol:FANCA
Accession:NM_001018112
Location:INTRON

Gene Symbol:FANCA
Accession:NM_001286167
Location:INTRON

Gene Symbol:FANCA
Accession:NM_001351830
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001709230 CLINVAR
dbSNP (RS) rs7202091 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FANCA CLINVAR
OMIM 607139 CLINVAR