RGD:405138797 Rat Genome Database

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Variant: RGD:405138797 -  Homo sapiens

RGD ID: 405138797
ClinVar ID: CV3045344
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DEAF1  LOC126861109  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 674,691
GRCh38 11 674,691
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001293634.1:c.1081C>A
NM_021008.4:c.1348C>A
NM_001367390.1:c.622C>A
NG_034156.2:g.37393C>A
More... 		12/09/2022 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003725469 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DEAF1 CLINVAR
  LOC126861109 CLINVAR
OMIM 602635 CLINVAR