All variants in the WWOX gene

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

3 entries on 1 page. Showing entries 1 - 3.
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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.358C>T r.(?) p.(Arg120Trp) - likely benign g.78149000C>T g.78115103C>T WWOX(NM_016373.3):c.358C>T (p.R120W) - WWOX_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
-?/. - c.358C>T r.(?) p.(Arg120Trp) - likely benign g.78149000C>T g.78115103C>T - - WWOX_000017 77 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs141361080 Germline - 77/2795 individuals - 0 - Mohammed Faruq
-?/. - c.358C>T r.(?) p.(Arg120Trp) - likely benign g.78149000C>T g.78115103C>T - - WWOX_000017 2 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs141361080 Germline - 2/2795 individuals - 0 - Mohammed Faruq
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