rs964106425 Rat Genome Database

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Variant: rs964106425 -  Homo sapiens

RGD ID: 28908168
RS ID: rs964106425
ClinVar ID: CV867795
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCF  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 22,645,904
GRCh38 11 22,624,358
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_022725.3:c.*328C>T
LRG_527t1:c.*328C>T
NM_022725.4:c.*328C>T
LRG_527:g.6484C>T
More... 		01/13/2018 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 RCV001107669 CLINVAR
dbSNP (RS) rs964106425 CLINVAR
MedGen C3469526 CLINVAR
NCBI Gene FANCF CLINVAR
OMIM 603467 CLINVAR
  613897 CLINVAR