ClinVar Miner

Submissions for variant NM_005055.5(RAPSN):c.650G>A (p.Arg217His)

gnomAD frequency: 0.00002  dbSNP: rs763058066
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001906986 SCV002183655 uncertain significance Fetal akinesia deformation sequence 1; Congenital myasthenic syndrome 11 2022-08-31 criteria provided, single submitter clinical testing This sequence change replaces arginine, which is basic and polar, with histidine, which is basic and polar, at codon 217 of the RAPSN protein (p.Arg217His). This variant is present in population databases (rs763058066, gnomAD 0.0009%). This variant has not been reported in the literature in individuals affected with RAPSN-related conditions. ClinVar contains an entry for this variant (Variation ID: 1406773). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). 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.
Revvity Omics, Revvity RCV003130594 SCV003813709 uncertain significance not provided 2021-05-26 criteria provided, single submitter clinical testing

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