ClinVar Miner

Submissions for variant NM_017837.4(PIGV):c.728T>C (p.Leu243Pro)

dbSNP: rs771841963
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago RCV000768045 SCV000898880 uncertain significance Hyperphosphatasia with intellectual disability syndrome 1 2021-03-30 criteria provided, single submitter clinical testing PIGV NM_017837 exon 3 p.Leu243Pro (c.728T>C): This variant has not been reported in the literature and is not present in large control databases. Evolutionary conservation and computational predictive tools suggest that this variant may impact the protein. In summary, data on this variant is insufficient for disease classification. Therefore, the clinical significance of this variant is uncertain.

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