| 基因名 | 突变 |
|---|---|
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186037119G>A,c.7859G>A,p.R2620Q |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186036974A>G,c.7714A>G,p.T2572A |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186034508T>C,c.7652T>C,p.L2551S |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186026474T>C,c.7253T>C,p.I2418T |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186024710C>A,c.7048C>A,p.L2350M |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186024657C>G,c.6995C>G,p.P2332R |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186024643G>A,c.6981G>A,p.M2327I |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186024579G>A,c.6917G>A,p.R2306Q |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186024570T>C,c.6908T>C,p.I2303T |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186008031G>C,c.5922G>C,p.Q1974H |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:186007997G>T,c.5888G>T,p.G1963V |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185992205T>C,c.5669T>C,p.L1890S |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185988684A>G,c.5482A>G,p.I1828V |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185987341A>G,c.5327A>G,p.D1776G |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185984488G>A,c.4828G>A,p.V1610I |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185984375G>A,c.4715G>A,p.R1572Q |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185976370A>G,c.4586A>G,p.N1529S |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185976348C>T,c.4564C>T,p.R1522C |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185976299C>G,c.4515C>G,p.D1505E |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185972940C>T,c.4439C>T,p.T1480I |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185972895T>G,c.4394T>G,p.V1465G |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185972883A>G,c.4382A>G,p.N1461S |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185969311A>T,c.4009A>T,p.I1337F |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185964136C>T,c.3695C>T,p.T1232M |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185963992T>C,c.3551T>C,p.V1184A |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185963991G>T,c.3550G>T,p.V1184F |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185958737A>G,c.3166A>G,p.T1056A |
| HMCN1(NM_031935,hemicentin 1,5635aa) | g.1:185956648A>T,c.3020A>T,p.N1007I |