Agent Commons Collaborative Research
NTHL1-deficiency tumor predisposition syndrome
rareBiallelic 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
- Part of
- Hereditary neoplastic syndrome
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