Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001225451 | SCV001397732 | pathogenic | not provided | 2023-02-04 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Ile639Argfs*12) in the LRPPRC gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in LRPPRC are known to be pathogenic (PMID: 26510951). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with LRPPRC-related conditions. ClinVar contains an entry for this variant (Variation ID: 953194). For these reasons, this variant has been classified as Pathogenic. |