Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV004223186 | SCV003719946 | uncertain significance | not specified | 2022-06-24 | criteria provided, single submitter | clinical testing | The c.1702G>A (p.A568T) alteration is located in exon 15 (coding exon 12) of the CEP250 gene. This alteration results from a G to A substitution at nucleotide position 1702, causing the alanine (A) at amino acid position 568 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. |