ClinVar Miner

Submissions for variant NC_000012.12:g.121641596G>C

dbSNP: rs1555324170
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001985258 SCV002224718 uncertain significance Combined immunodeficiency due to ORAI1 deficiency; Myopathy, tubular aggregate, 2 2021-08-31 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals with ORAI1-related conditions. 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant is not present in population databases (ExAC no frequency). This sequence change replaces aspartic acid with histidine at codon 287 of the ORAI1 protein (p.Asp287His). The aspartic acid residue is highly conserved and there is a moderate physicochemical difference between aspartic acid and histidine.

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