RGD:405189574 Rat Genome Database

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Variant: RGD:405189574 -  Homo sapiens

RGD ID: 405189574
ClinVar ID: CV3156730
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DEAF1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 678,819
GRCh38 11 678,819
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021008.4:c.1130A>G
NM_001367390.1:c.404A>G
NM_001293634.1:c.863A>G
NG_034156.2:g.33265A>G
More... 		01/21/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003859608 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DEAF1 CLINVAR
OMIM 602635 CLINVAR