Full data view for gene USP9X

Information The variants shown are described using the NM_001039590.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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     
?/? 16 c.2004T>A r.(?) p.(=) Maternal (inferred) - - g.41025143T>A g.41165890T>A 1983T>A (G661G) - USP9X_000001 recurrent, found 4 times PubMed: Tarpey 2009 - - Germline ? 4/208 cases - 0 - DNA SEQ ? - MRX;IDX 19377116-Pat? PubMed: Tarpey 2009 . M ? - - - 0 for details contact Lucy Raymond (flr24 @ cam.ac.uk) - 4 Lucy Raymond
-?/. - c.2004T>A r.(?) p.(=) Unknown - likely benign g.41025143T>A - USP9X(NM_001039590.2):c.2004T>A (p.G668=) - USP9X_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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