ClinVar Miner

Submissions for variant NM_000127.3(EXT1):c.249dup (p.Gln84fs)

dbSNP: rs2488052905
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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 RCV003498023 SCV004247090 pathogenic Multiple congenital exostosis 2024-04-24 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Gln84Alafs*105) in the EXT1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in EXT1 are known to be pathogenic (PMID: 10679937, 11391482, 19810120). This variant is not present in population databases (gnomAD no frequency). This premature translational stop signal has been observed in individuals with multiple osteochondromatosis (PMID: 11432960, 25230886). For these reasons, this variant has been classified as Pathogenic.

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