ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.605T>C (p.Ile202Thr)

gnomAD frequency: 0.00002  dbSNP: rs751126921
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001351677 SCV001546170 uncertain significance Fanconi anemia 2021-08-20 criteria provided, single submitter clinical testing This sequence change replaces isoleucine with threonine at codon 202 of the FANCD2 protein (p.Ile202Thr). The isoleucine residue is weakly conserved and there is a moderate physicochemical difference between isoleucine and threonine. This variant is present in population databases (rs751126921, ExAC 0.001%). This variant has not been reported in the literature in individuals affected with FANCD2-related conditions. 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. 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 RCV001788465 SCV002030253 uncertain significance Fanconi anemia complementation group D2 2021-03-02 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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