rs181285048 Rat Genome Database

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Variant: rs181285048 -  Homo sapiens

RGD ID: 28900711
RS ID: rs181285048
ClinVar ID: CV867784
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCF  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 22,644,748
GRCh38 11 22,623,202
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_527t1:c.*1484G>A
NM_022725.4:c.*1484G>A
LRG_527:g.7640G>A
NG_007425.1:g.7640G>A
More... 		01/12/2018 3 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001103950 CLINVAR
dbSNP (RS) rs181285048 CLINVAR
MedGen C3469526 CLINVAR
NCBI Gene FANCF CLINVAR
OMIM 603467 CLINVAR
  613897 CLINVAR