ClinVar Miner

Submissions for variant NM_013382.7(POMT2):c.1300del (p.Arg434fs)

dbSNP: rs2140188352
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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 RCV001933393 SCV002197331 pathogenic Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2; Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2; Autosomal recessive limb-girdle muscular dystrophy type 2N 2021-10-20 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Arg434Glyfs*11) in the POMT2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in POMT2 are known to be pathogenic (PMID: 15894594). For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals affected with POMT2-related conditions. This variant is not present in population databases (ExAC no frequency).

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