ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.810del (p.Ser271fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005026357 SCV005655484 likely pathogenic Peutz-Jeghers syndrome; Melanoma, cutaneous malignant, susceptibility to, 1; Familial pancreatic carcinoma; Germ cell tumor of testis 2024-03-28 criteria provided, single submitter clinical testing

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