ClinVar Miner

Submissions for variant NM_001271208.2(NEB):c.24276G>T (p.Met8092Ile) (rs758996758)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000800597 SCV000940323 uncertain significance Nemaline myopathy 2 2019-07-19 criteria provided, single submitter clinical testing This sequence change replaces methionine with isoleucine at codon 8092 of the NEB protein (p.Met8092Ile). The methionine residue is weakly conserved and there is a small physicochemical difference between methionine and isoleucine. This variant is present in population databases (rs758996758, ExAC 0.01%). This variant has not been reported in the literature in individuals with NEB-related disease. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Not Available"; PolyPhen-2: "Not Available"; Align-GVGD: "Class C0". The isoleucine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. These predictions have not been confirmed by published functional studies and their clinical significance is uncertain. 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.
Natera, Inc. RCV000800597 SCV001459169 uncertain significance Nemaline myopathy 2 2020-09-16 no assertion criteria provided clinical testing

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