RGD:405198268 Rat Genome Database

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Variant: RGD:405198268 -  Homo sapiens

RGD ID: 405198268
ClinVar ID: CV2973057
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DEAF1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 684,933
GRCh38 11 684,933
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001367390.1:c.109T>C
NM_001293634.1:c.695T>C
NM_021008.4:c.835T>C
NG_034156.2:g.27151T>C
More... 		04/10/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003677912 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DEAF1 CLINVAR
OMIM 602635 CLINVAR