Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Pediatric Genomic Medicine, |
RCV000515120 | SCV000609662 | likely benign | not provided | 2017-04-03 | criteria provided, single submitter | clinical testing | |
Wong Mito Lab, |
RCV000854791 | SCV000997835 | benign | Leigh syndrome | 2019-10-17 | criteria provided, single submitter | clinical testing | The NC_012920.1:m.12346C>T (YP_003024036.1:p.His4Tyr) variant in MTND5 gene is interpretated to be a Benign variant based on the modified ACMG guidelines (unpublished). This variant meets the following evidence codes: BA1 |