ClinVar Miner

Submissions for variant NM_001378454.1(ALMS1):c.2896C>T (p.Gln966Ter)

dbSNP: rs761177629
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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 RCV001384822 SCV001584472 pathogenic Alstrom syndrome 2022-12-16 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 1072171). This variant has not been reported in the literature in individuals affected with ALMS1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Gln967*) in the ALMS1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in ALMS1 are known to be pathogenic (PMID: 17594715). For these reasons, this variant has been classified as Pathogenic.

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