rs886048148 Rat Genome Database

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Variant: rs886048148 -  Homo sapiens

RGD ID: 11651730
RS ID: rs886048148
ClinVar ID: CV319945
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCF  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 22,644,161
GRCh38 11 22,622,615
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_527t1:c.*2071A>G
LRG_527:g.8227A>G
NG_007425.1:g.8227A>G
NC_000011.10:g.22622615T>C
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 RCV000300730 CLINVAR
dbSNP (RS) rs886048148 CLINVAR
MedGen C3469526 CLINVAR
NCBI Gene FANCF CLINVAR
OMIM 603467 CLINVAR
  613897 CLINVAR