All variants in the USP26 gene

Information The variants shown are described using the NM_031907.1 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.1976C>T r.(?) p.(Thr659Met) - likely benign g.132160273G>A g.133026245G>A - - USP26_000008 - PubMed: Papuc 2019 - rs145695346 Germline - - - 0 - Anaïs Begemann
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