Journal of Forensic Medicine ›› 2025, Vol. 41 ›› Issue (1): 85-88.DOI: 10.12116/j.issn.1004-5619.2023.430802
• Case Reports • Previous Articles Next Articles
Received:2023-08-08
Online:2025-05-19
Published:2025-02-25
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URL: http://www.fyxzz.cn/EN/10.12116/j.issn.1004-5619.2023.430802
| 编号 | 变异基因 | 相关疾病 | ACMG预测结果 |
|---|---|---|---|
| 1 | AKAP9(p.Arg3237Trp) | 长QT间期综合征Ⅱ型(AD) | 意义不明确 |
| 2 | NOTCH2(p.Ala1403Thr) | Alagille综合征2型(AD)、Hajdu-Cheney综合征(AD) | 意义不明确 |
| 3 | TRRAP(p.Ile924Val) | 伴有或不伴有畸形相和自闭症的发育迟缓(AD) | 意义不明确 |
| 4 | ACADVL (p.Met352Thr) (p.Ser423=) | VLCADD(AR) | 意义不明确 意义不明确 |
| 5 | SETBP1(p.Ala630Val) | Schinzel-Giedion面中部回缩综合征(AD)、常染色体显性遗传性智力发育障碍29型(AD) | 意义不明确 |
| 6 | TBX1(p.Ala393Thr) | Digeorge综合征(AD)、法洛四联症(AD) | 意义不明确 |
| 7 | SLCO2A1(Intron) | 原发肥大性骨关节病(AR) | 可能致病 |
| 8 | LRP2(p.Asn3472LysfsTer31) | Donnai-Barrow综合征(AR) | 可能致病 |
| 9 | CLDN1(Intron) | 新生儿鱼鳞病-硬化性胆管炎综合征(AR) | 可能致病 |
| 10 | DIS3L2(p.Ala315Ser) | Perlman综合征(AR) | 意义不明确 |
| 11 | MEGF10(p.Ala654Thr) | 肌病,反射消失,呼吸窘迫,吞咽困难,早发型(AR) | 意义不明确 |
Tab. 1 Nuclear gene variants detected by whole-genome sequencing
| 编号 | 变异基因 | 相关疾病 | ACMG预测结果 |
|---|---|---|---|
| 1 | AKAP9(p.Arg3237Trp) | 长QT间期综合征Ⅱ型(AD) | 意义不明确 |
| 2 | NOTCH2(p.Ala1403Thr) | Alagille综合征2型(AD)、Hajdu-Cheney综合征(AD) | 意义不明确 |
| 3 | TRRAP(p.Ile924Val) | 伴有或不伴有畸形相和自闭症的发育迟缓(AD) | 意义不明确 |
| 4 | ACADVL (p.Met352Thr) (p.Ser423=) | VLCADD(AR) | 意义不明确 意义不明确 |
| 5 | SETBP1(p.Ala630Val) | Schinzel-Giedion面中部回缩综合征(AD)、常染色体显性遗传性智力发育障碍29型(AD) | 意义不明确 |
| 6 | TBX1(p.Ala393Thr) | Digeorge综合征(AD)、法洛四联症(AD) | 意义不明确 |
| 7 | SLCO2A1(Intron) | 原发肥大性骨关节病(AR) | 可能致病 |
| 8 | LRP2(p.Asn3472LysfsTer31) | Donnai-Barrow综合征(AR) | 可能致病 |
| 9 | CLDN1(Intron) | 新生儿鱼鳞病-硬化性胆管炎综合征(AR) | 可能致病 |
| 10 | DIS3L2(p.Ala315Ser) | Perlman综合征(AR) | 意义不明确 |
| 11 | MEGF10(p.Ala654Thr) | 肌病,反射消失,呼吸窘迫,吞咽困难,早发型(AR) | 意义不明确 |
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