ClinVar Miner

Submissions for variant NM_001378454.1(ALMS1):c.7256C>T (p.Ala2419Val)

dbSNP: rs1672001133
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002008446 SCV002275244 uncertain significance Alstrom syndrome 2022-06-04 criteria provided, single submitter clinical testing This sequence change replaces alanine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 2420 of the ALMS1 protein (p.Ala2420Val). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with ALMS1-related conditions. ClinVar contains an entry for this variant (Variation ID: 1485154). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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.
Fulgent Genetics, Fulgent Genetics RCV002008446 SCV002785683 uncertain significance Alstrom syndrome 2022-01-06 criteria provided, single submitter clinical testing

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