DNAH14 | Mutation | Missense | ENST00000430092.1 |
g.225239246G>A
|
c.2173G>A
|
p.Ala725Thr
|
probably damaging
| SNU475 |
DNAH14 | Mutation | Missense | ENST00000430092.1 |
g.225534194T>C
|
c.10855T>C
|
p.Cys3619Arg
|
probably damaging
| Li7 |
DNAH14 | Mutation | Missense | ENST00000430092.1 |
g.225334903C>T
|
c.4841C>T
|
p.Ala1614Val
|
probably damaging
| JHH5 |
DNAH14 | Mutation | Missense | ENST00000430092.1 |
g.225284926C>T
|
c.3680C>T
|
p.Ser1227Phe
|
probably damaging
| SNU368 |
DNAH14 | Mutation | Missense | ENST00000430092.1 |
g.225534194T>C
|
c.10855T>C
|
p.Cys3619Arg
|
probably damaging
| SNU368 |
DNAH14 | Mutation | Missense | ENST00000430092.1 |
g.225239246G>A
|
c.2173G>A
|
p.Ala725Thr
|
probably damaging
| SNU878 |
DNAH14 | Mutation | Missense | ENST00000430092.1 |
g.225380540A>G
|
c.5747A>G
|
p.Tyr1916Cys
|
benign
| SNU878 |