ClinVar Miner

Submissions for variant NM_001384125.1(BLTP1):c.3925C>T (p.Arg1309Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003988584 SCV004803891 pathogenic Alkuraya-Kucinskas syndrome 2024-01-19 criteria provided, single submitter clinical testing Variant summary: KIAA1109 c.3925C>T (p.Arg1309X) results in a premature termination codon, predicted to cause a truncation of the encoded protein or absence of the protein due to nonsense mediated decay, which are commonly known mechanisms for disease. The variant allele was found at a frequency of 4e-06 in 249486 control chromosomes (gnomAD). To our knowledge, no occurrence of c.3925C>T in individuals affected with Alkuraya-Kucinskas Syndrome and no experimental evidence demonstrating its impact on protein function have been reported. No submitters have cited clinical-significance assessments for this variant to ClinVar. Based on the evidence outlined above, the variant was classified as pathogenic.

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