Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000443681 | SCV000512162 | likely benign | not specified | 2017-11-27 | criteria provided, single submitter | clinical testing | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. |
Labcorp Genetics |
RCV001089223 | SCV000558425 | likely benign | Ataxia-telangiectasia syndrome | 2024-02-01 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV000590322 | SCV000694286 | uncertain significance | not provided | 2015-10-22 | criteria provided, single submitter | clinical testing | Variant summary: ATM c.4611+9C>G affects a non-conserved nucleotide, Mutation Taster predicts the change is a polymorphism, and 4/5 Alamut algorithms predict no significant change to splicing. This variant was found in 2/121332 control chromosomes at a frequency of 0.0000165, which does not significantly exceed maximal expected frequency of a pathogenic ATM allele (0.0039528). The variant of interest has not been reported in affected individuals via publications and/or reputable databases/clinical laboratories; nor evaluated for functional impact by in vivo/vitro studies. Because of the absence of clinical information and the lack of functional studies, the variant was classified as a variant of uncertain significance (VUS) until additional information becomes available. |
Color Diagnostics, |
RCV000773191 | SCV000906763 | likely benign | Hereditary cancer-predisposing syndrome | 2016-08-15 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV004591152 | SCV005085062 | likely benign | Familial cancer of breast | 2024-05-20 | criteria provided, single submitter | clinical testing | This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing. |