ClinVar Miner

Submissions for variant NM_002480.3(PPP1R12A):c.508C>T (p.Arg170Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Department, Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology RCV003986010 SCV004801839 likely pathogenic Genitourinary and/or brain malformation syndrome criteria provided, single submitter clinical testing A previously undescribed nucleotide variant creates a premature translation stop signal p.Arg170Ter in the PPP1R12A gene. The variant was observed in heterozygous state in an individual affected with sex reversal and genounitary malformations. Loss-of-function variants are reported in patients with Genitourinary and/or/brain malformation syndrome, 618820, [Hughes et al., 2020, PMID: 31883643]. The variant is not present in population database (gnomAD no frequency). In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as likely pathogenic.

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