ClinVar Miner

Submissions for variant NM_001379110.1(SLC9A6):c.1832C>T (p.Thr611Ile)

dbSNP: rs2071564662
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001237236 SCV001409989 uncertain significance Christianson syndrome 2019-07-28 criteria provided, single submitter clinical testing 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. This variant has not been reported in the literature in individuals with SLC9A6-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces threonine with isoleucine at codon 601 of the SLC9A6 protein (p.Thr601Ile). The threonine residue is moderately conserved and there is a moderate physicochemical difference between threonine and isoleucine.

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