ClinVar Miner

Submissions for variant NM_001378454.1(ALMS1):c.3576C>G (p.Tyr1192Ter)

gnomAD frequency: 0.00001  dbSNP: rs1671899045
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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 RCV001950787 SCV002236788 pathogenic Alstrom syndrome 2022-08-19 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 1455696). This premature translational stop signal has been observed in individual(s) with Alstrom syndrome (PMID: 25846608, 30064963). This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Tyr1193*) 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).

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