rs45473997 Rat Genome Database

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Variant: rs45473997 -  Homo sapiens

RGD ID: 150429032
RS ID: rs45473997
ClinVar ID: CV1187731
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCF  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 22,646,046
GRCh38 11 22,624,500
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_022725.4:c.*186T>G
LRG_527:g.6342T>G
NG_007425.1:g.6342T>G
NC_000011.10:g.22624500A>C
More... 		03/20/2019 3 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FANCF
Accession:NM_022725
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001563061 CLINVAR
dbSNP (RS) rs45473997 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FANCF CLINVAR
OMIM 613897 CLINVAR