All variants in the WWOX gene

Information The variants shown are described using the NM_016373.2 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
./. - c.1222C>T r.(?) p.(Arg408Trp) - VUS g.79245670C>T g.79211773C>T - - WWOX_000012 - PubMed: Bobbili 2018, Journal: Bobbili 2018 - rs144234059 Germline - 1/194 cases RE - 0 - Dheeraj Bobbili
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