ClinVar Miner

Submissions for variant NM_001003841.3(SLC6A19):c.683C>T (p.Thr228Met)

gnomAD frequency: 0.00037  dbSNP: rs762412163
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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 RCV002003044 SCV002272887 uncertain significance not provided 2022-07-20 criteria provided, single submitter clinical testing This sequence change replaces threonine, which is neutral and polar, with methionine, which is neutral and non-polar, at codon 228 of the SLC6A19 protein (p.Thr228Met). This variant is present in population databases (rs762412163, gnomAD 0.07%). This variant has not been reported in the literature in individuals affected with SLC6A19-related conditions. ClinVar contains an entry for this variant (Variation ID: 1482946). 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: "Probably Damaging"; Align-GVGD: "Class C0"). 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.
Fulgent Genetics, Fulgent Genetics RCV002492232 SCV002793924 uncertain significance Hyperglycinuria; Neutral 1 amino acid transport defect; Iminoglycinuria 2022-05-25 criteria provided, single submitter clinical testing

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