Total submissions: 1
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Laboratory for Molecular Medicine, |
RCV000038334 | SCV000062005 | uncertain significance | not specified | 2010-11-03 | criteria provided, single submitter | clinical testing | Variant classified as Uncertain Significance - Favor Pathogenic. The 616+1G>A va riant has not been reported in the literature. This variant is predicted to cau se abnormal splicing because the nucleotide substitution occurs in the highly co nserved splice consensus sequence. Splice variants can lead to aberrant, truncat ed, or absent protein and in most genes, are typically assumed to be disease cau sing. However, all disease causing variants in the ACTC gene known to date are missense variants and it is therefore unclear whether abnormal splicing can lead to disease. However, this individual's racial origin is reported to be Caucasia n and the 616+1G>A variant has not been identified in over 1500 Caucasian proban ds (3000 chromosomes) tested by our laboratory. Although we cannot exclude the p ossibility that this variant could be benign, this low frequency increases the l ikelihood that it is pathogenic. In summary, additional studies (healthy control studies and/or family studies) are necessary to determine the significance of t he 616+1 variant. |