ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.398C>T (p.Pro133Leu)

dbSNP: rs139382920
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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 RCV001062932 SCV001227758 uncertain significance Fanconi anemia 2019-12-11 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: "Possibly Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with FANCM-related conditions. This variant is present in population databases (rs139382920, ExAC 0.01%). This sequence change replaces proline with leucine at codon 133 of the FANCM protein (p.Pro133Leu). The proline residue is moderately conserved and there is a moderate physicochemical difference between proline and leucine.
Fulgent Genetics, Fulgent Genetics RCV002482072 SCV002783577 uncertain significance Spermatogenic failure 28; Premature ovarian failure 15 2022-04-25 criteria provided, single submitter clinical testing

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