ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.3539dup (p.Tyr1180Ter)

dbSNP: rs1891145931
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001203402 SCV001374565 pathogenic DICER1-related tumor predisposition 2024-01-05 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Tyr1180*) in the DICER1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in DICER1 are known to be pathogenic (PMID: 19556464, 21266384). This variant is not present in population databases (gnomAD no frequency). This premature translational stop signal has been observed in individual(s) with DICER1-related conditions (PMID: 30178239). ClinVar contains an entry for this variant (Variation ID: 934917). For these reasons, this variant has been classified as Pathogenic.

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