Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV003251542 | SCV003937158 | uncertain significance | Inborn genetic diseases | 2023-05-24 | criteria provided, single submitter | clinical testing | The c.4472A>G (p.K1491R) alteration is located in exon 12 (coding exon 11) of the SLX4 gene. This alteration results from a A to G substitution at nucleotide position 4472, causing the lysine (K) at amino acid position 1491 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. |