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.1238C>A r.(?) p.(Ser413Tyr) - benign g.79245686C>A g.79211789C>A - - WWOX_000051 27 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs117065412 Germline - 27/2794 individuals - 0 - Mohammed Faruq
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