ClinVar Miner

Submissions for variant NM_022173.4(TIA1):c.805G>A (p.Val269Ile)

dbSNP: rs1678158814
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001303177 SCV001492416 uncertain significance Welander distal myopathy 2020-07-08 criteria provided, single submitter clinical testing This sequence change replaces valine with isoleucine at codon 269 of the TIA1 protein (p.Val269Ile). The valine residue is highly conserved and there is a small physicochemical difference between valine and isoleucine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with TIA1-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated, but 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.

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