Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001857844 | SCV002238933 | pathogenic | not provided | 2024-01-24 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Arg207*) in the DYNC2LI1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in DYNC2LI1 are known to be pathogenic (PMID: 26077881, 26130459). This variant is present in population databases (rs745930390, gnomAD 0.04%). This premature translational stop signal has been observed in individual(s) with clinical features of DYNC2LI1-related conditions (PMID: 26130459). This variant is also known as p.Arg208Ter. ClinVar contains an entry for this variant (Variation ID: 253218). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. For these reasons, this variant has been classified as Pathogenic. |
OMIM | RCV000239659 | SCV000298012 | pathogenic | Short-rib thoracic dysplasia 15 with polydactyly | 2018-04-06 | no assertion criteria provided | literature only |