rs61889392 Rat Genome Database

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Variant: rs61889392 -  Homo sapiens

RGD ID: 11606892
RS ID: rs61889392
ClinVar ID: CV313760
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCF  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 22,645,524
GRCh38 11 22,623,978
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_527t1:c.*708C>T
LRG_527:g.6864C>T
NG_007425.1:g.6864C>T
NC_000011.10:g.22623978G>A
More... 		01/12/2018 3 prime utr variant uncertain significance
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 RCV000337277 CLINVAR
dbSNP (RS) rs61889392 CLINVAR
MedGen C3469526 CLINVAR
NCBI Gene FANCF CLINVAR
OMIM 603467 CLINVAR
  613897 CLINVAR