ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.2662C>T (p.Arg888Trp)

gnomAD frequency: 0.00001  dbSNP: rs1237984655
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002020403 SCV002289458 uncertain significance Gastrointestinal stromal tumor 2023-08-28 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. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be disruptive. ClinVar contains an entry for this variant (Variation ID: 1505172). This variant has not been reported in the literature in individuals affected with KIT-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.006%). This sequence change replaces arginine, which is basic and polar, with tryptophan, which is neutral and slightly polar, at codon 888 of the KIT protein (p.Arg888Trp).
Baylor Genetics RCV002020403 SCV004198095 uncertain significance Gastrointestinal stromal tumor 2023-09-26 criteria provided, single submitter clinical testing

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