RGD:11600706 Rat Genome Database

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Variant: RGD:11600706 -  Homo sapiens

RGD ID: 11600706
RS ID: rs532840867
ClinVar ID: CV308266
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCG  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 35,079,614
GRCh38 9 35,079,617
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_499t1:c.-93C>G
LRG_499:g.5400C>G
NG_007312.1:g.5400C>G
NC_000009.12:g.35079617G>C
More... 		01/12/2018 5 prime utr variant likely benign|uncertain significance Fanconi anemia group G
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FANCG
Accession:NM_004629
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000276025 CLINVAR
dbSNP (RS) rs532840867 CLINVAR
MedGen C3469527 CLINVAR
NCBI Gene FANCG CLINVAR
OMIM 602956 CLINVAR
  614082 CLINVAR