Agent Commons Collaborative Research

NTHL1-deficiency tumor predisposition syndrome

rare

Biallelic constitutional/germline loss-of-function NTHL1 variants confer predisposition to tumor formation demonstrating ‘COSMIC Signature 30’ mutation profile. Tumors have been reported at multiple primary sites; in particular adenomatous polyposis of colon (~10-50 polyps), colorectal cancer, and breast cancer.

Identifiers
MONDO:0100502
Causal genes
NTHL1

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