ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.10_11delinsTT (p.Ala4Phe)

dbSNP: rs1553881759
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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 RCV000633790 SCV000755063 uncertain significance Gastrointestinal stromal tumor 2023-11-24 criteria provided, single submitter clinical testing This sequence change replaces alanine, which is neutral and non-polar, with phenylalanine, which is neutral and non-polar, at codon 4 of the KIT protein (p.Ala4Phe). This variant is present in population databases (no rsID available, gnomAD 0.003%). This variant has not been reported in the literature in individuals affected with KIT-related conditions. ClinVar contains an entry for this variant (Variation ID: 528568). 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. 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.
Baylor Genetics RCV000633790 SCV005059798 uncertain significance Gastrointestinal stromal tumor 2024-03-24 criteria provided, single submitter clinical testing

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