Total submissions: 9
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Illumina Laboratory Services, |
RCV000386833 | SCV000452992 | uncertain significance | Myofibrillar Myopathy, Dominant | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Illumina Laboratory Services, |
RCV000874867 | SCV000452993 | uncertain significance | Myofibrillar myopathy 3 | 2018-01-13 | criteria provided, single submitter | clinical testing | This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease. |
Illumina Laboratory Services, |
RCV000347504 | SCV000452994 | uncertain significance | Limb-Girdle Muscular Dystrophy, Dominant | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Eurofins Ntd Llc |
RCV000594719 | SCV000705997 | likely benign | not specified | 2017-01-30 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000874867 | SCV001017099 | benign | Myofibrillar myopathy 3 | 2024-01-03 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001557068 | SCV001778766 | likely benign | not provided | 2020-11-09 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002523507 | SCV003687379 | uncertain significance | Inborn genetic diseases | 2021-08-02 | criteria provided, single submitter | clinical testing | The c.533G>A (p.R178H) alteration is located in exon 4 (coding exon 3) of the MYOT gene. This alteration results from a G to A substitution at nucleotide position 533, causing the arginine (R) at amino acid position 178 to be replaced by a histidine (H). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV000594719 | SCV004038169 | likely benign | not specified | 2023-08-19 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003950243 | SCV004765033 | likely benign | MYOT-related disorder | 2020-08-10 | criteria provided, single submitter | clinical testing | This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |