Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000799194 | SCV000938847 | pathogenic | Neurofibromatosis, type 1 | 2020-01-31 | criteria provided, single submitter | clinical testing | For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in NF1 are known to be pathogenic (PMID: 10712197, 23913538). This variant has not been reported in the literature in individuals with NF1-related disease. ClinVar contains an entry for this variant (Variation ID: 645159). This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Glu1811Asnfs*31) in the NF1 gene. It is expected to result in an absent or disrupted protein product. |