Total submissions: 7
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000117195 | SCV000168776 | benign | not specified | 2014-03-06 | 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. |
Invitae | RCV001083408 | SCV000562287 | benign | Intellectual disability, autosomal dominant 6; Developmental and epileptic encephalopathy, 27 | 2024-01-30 | criteria provided, single submitter | clinical testing | |
Athena Diagnostics | RCV000084727 | SCV000842283 | benign | not provided | 2017-10-25 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002313840 | SCV000847482 | benign | Inborn genetic diseases | 2016-08-05 | criteria provided, single submitter | clinical testing | This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. |
Fulgent Genetics, |
RCV001083408 | SCV002811986 | likely benign | Intellectual disability, autosomal dominant 6; Developmental and epileptic encephalopathy, 27 | 2021-09-27 | criteria provided, single submitter | clinical testing | |
Psychiatry Genetics Yale University | RCV000084727 | SCV000116863 | not provided | not provided | no assertion provided | not provided | ||
Genetic Services Laboratory, |
RCV000117195 | SCV000151359 | likely benign | not specified | no assertion criteria provided | clinical testing | Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated disease phenotype. NOT Sanger confirmed. |