ClinVar Miner

Submissions for variant NM_022489.4(INF2):c.1892C>T (p.Thr631Ile)

dbSNP: rs1595172697
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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 RCV001326575 SCV001517612 uncertain significance Focal segmental glomerulosclerosis 5; Charcot-Marie-Tooth disease dominant intermediate E 2021-06-08 criteria provided, single submitter clinical testing This sequence change replaces threonine with isoleucine at codon 631 of the INF2 protein (p.Thr631Ile). The threonine residue is moderately conserved and there is a moderate physicochemical difference between threonine and isoleucine. This variant is not present in population databases (ExAC no frequency). 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 INF2-related conditions.

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