ClinVar Miner

Submissions for variant NM_025132.4(WDR19):c.1810G>T (p.Val604Phe)

dbSNP: rs1245108212
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001912963 SCV002172931 uncertain significance Asphyxiating thoracic dystrophy 5; Senior-Loken syndrome 8 2021-06-18 criteria provided, single submitter clinical testing 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. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with WDR19-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces valine with phenylalanine at codon 604 of the WDR19 protein (p.Val604Phe). The valine residue is weakly conserved and there is a small physicochemical difference between valine and phenylalanine.

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