RGD:405236656 Rat Genome Database

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Variant: RGD:405236656 -  Homo sapiens

RGD ID: 405236656
ClinVar ID: CV3166436
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCE  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 35,423,800
GRCh38 6 35,456,023
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_498t1:c.525C>T
NM_007104.1:c.-12412C>T
NM_001410876.1:c.525C>T
NM_021922.3:c.525C>T
More... 		06/23/2023 synonymous variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003853885 CLINVAR
MedGen C3160739 CLINVAR
NCBI Gene FANCE CLINVAR
OMIM 600901 CLINVAR
  613976 CLINVAR