RGD:11620050 Rat Genome Database

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Variant: RGD:11620050 -  Homo sapiens

RGD ID: 11620050
RS ID: rs16909782
ClinVar ID: CV326157
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCF  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 22,646,126
GRCh38 11 22,624,580
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_527t1:c.*106T>C
LRG_527:g.6262T>C
NG_007425.1:g.6262T>C
NC_000011.10:g.22624580A>G
More...
01/12/2018 3 prime utr variant benign|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 RCV000332044 CLINVAR
dbSNP (RS) rs16909782 CLINVAR
MedGen C3469526 CLINVAR
NCBI Gene FANCF CLINVAR
OMIM 603467 CLINVAR
  613897 CLINVAR