Full data view for gene WWOX

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

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
./. - c.754C>G r.(?) p.(Pro252Ala) Unknown - VUS g.78458915C>G g.78425018C>G - - WWOX_000006 - PubMed: Bobbili 2018, Journal: Bobbili 2018 - rs75559202 Germline - 1/194 cases RE - 0 - DNA SEQ-NG - - epilepsy, Rolandic S_670:0/1:TYPICAL_RE PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 194 RE cases - - - - - 0 - - 1 Dheeraj Bobbili
-?/. - c.754C>G r.(?) p.(Pro252Ala) Unknown - likely benign g.78458915C>G g.78425018C>G WWOX(NM_016373.4):c.754C>G (p.P252A) - WWOX_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
Legend   How to query