Table 3. List of selected variants.
Patient | Gene | Sequence variants | State | References | ACMG evidence of pathogenity |
---|---|---|---|---|---|
1 | NEB | c.17779_17780delTA | Het | novel | Path |
c.11086A>C | Het | novel | VUS | ||
2 | NEB | c.21076C>T | Het | Lehtokari et al, 2014[15] | Path |
4 | NEB | c.2310+5G>A | Het | novel | Path |
c. 17779_17780delTA | Het | novel | Path | ||
5 | ACTA1 | c.871A>T | Het | Laing et al,2009[16] | Path |
Het: Heterozygote; Path: Pathogenic; VUS: Variant of Uncertain Significance