RGD:405181302 Rat Genome Database

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Variant: RGD:405181302 -  Homo sapiens

RGD ID: 405181302
ClinVar ID: CV2914142
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DEAF1  LOC127820019  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 686,889
GRCh38 11 686,889
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.47A>G
NM_001293634.1:c.664+1022A>G
NM_021008.4:c.773A>G
NG_034156.2:g.25195A>G
More...
01/25/2024 intron variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003563995 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DEAF1 CLINVAR
OMIM 602635 CLINVAR