Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001070852 | SCV001236129 | pathogenic | Neurofibromatosis, type 1 | 2019-12-10 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Leu1859*) in the NF1 gene. It is expected to result in an absent or disrupted protein product. This variant is not present in population databases (ExAC no frequency). This nonsense change has been observed in individuals with clinical features of Neurofibromatosis, type 1 (PMID: 28961165, Invitae). Loss-of-function variants in NF1 are known to be pathogenic (PMID: 10712197, 23913538). For these reasons, this variant has been classified as Pathogenic. |