ClinVar Miner

Submissions for variant NM_005655.4(KLF10):c.884C>A (p.Pro295His)

dbSNP: rs1827207489
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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 RCV001879249 SCV002139466 uncertain significance not provided 2021-03-07 criteria provided, single submitter clinical testing This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with KLF10-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 disruptive, 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. This sequence change replaces proline with histidine at codon 295 of the KLF10 protein (p.Pro295His). The proline residue is highly conserved and there is a moderate physicochemical difference between proline and histidine.

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