ClinVar Miner

Submissions for variant NM_012082.4(ZFPM2):c.364G>T (p.Val122Leu)

dbSNP: rs772114579
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000529779 SCV000659516 uncertain significance 46,XY sex reversal 9 2017-07-26 criteria provided, single submitter clinical testing This sequence change replaces valine with leucine at codon 122 of the ZFPM2 protein (p.Val122Leu). The valine residue is weakly conserved and there is a small physicochemical difference between valine and leucine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with ZFPM2-related disease. 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.
Revvity Omics, Revvity RCV003139869 SCV003826116 uncertain significance not provided 2019-01-15 criteria provided, single submitter clinical testing

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