RGD:407456042 Rat Genome Database

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Variant: RGD:407456042 -  Homo sapiens

RGD ID: 407456042
ClinVar ID: CV3415707
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DCDC1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 30,902,841
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001387275.1:c.1842C>A
NM_020869.4:c.2409C>A
NM_001367979.1:c.5088C>A
NM_001387274.1:c.5097C>A
More... 		07/22/2024 nonsense likely pathogenic

Variant Details
Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV004598584 CLINVAR
NCBI Gene DCDC1 CLINVAR
OMIM 608062 CLINVAR