ClinVar Miner

Submissions for variant NM_020975.6(RET):c.3247_3254del (p.Thr1083fs)

dbSNP: rs1838375749
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001316280 SCV001506889 uncertain significance Multiple endocrine neoplasia, type 2 2020-06-04 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals with RET-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change results in a premature translational stop signal in the RET gene (p.Thr1083Trpfs*8). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 32 amino acids of the RET protein.

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