RGD:405240355 Rat Genome Database

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Variant: RGD:405240355 -  Homo sapiens

RGD ID: 405240355
ClinVar ID: CV2882736
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DEAF1  LOC126861109  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 674,596
GRCh38 11 674,596
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.1176C>T
NM_021008.4:c.1443C>T
NM_001367390.1:c.717C>T
NG_034156.2:g.37488C>T
More... 		11/28/2022 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003557195 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DEAF1 CLINVAR
  LOC126861109 CLINVAR
OMIM 602635 CLINVAR