Variants
Found 10 variants in this database.
Variant ID |
Entrez Gene ID |
Gene |
Chromsome |
Start |
End |
Disease |
Method |
18214 |
112399 |
EGLN3 |
14 |
34710271 |
34710271 |
Asymptomatic
|
HiSeq X Ten
|
18223 |
112399 |
EGLN3 |
14 |
34530730 |
34530730 |
Asymptomatic
|
HiSeq X Ten
|
18271 |
112399 |
EGLN3 |
14 |
34674402 |
34674402 |
Asymptomatic
|
HiSeq X Ten
|
18318 |
112399 |
EGLN3 |
14 |
34720184 |
34720184 |
Asymptomatic
|
HiSeq X Ten
|
18507 |
112399 |
EGLN3 |
14 |
34725703 |
34725703 |
Asymptomatic
|
HiSeq X Ten
|
18521 |
112399 |
EGLN3 |
14 |
34896483 |
34896483 |
Asymptomatic
|
HiSeq X Ten
|
18537 |
112399 |
EGLN3 |
14 |
34453927 |
34453927 |
Asymptomatic
|
HiSeq X Ten
|
18592 |
112399 |
EGLN3 |
14 |
34582811 |
34582811 |
Cockayne syndrome
|
HiSeq X Ten
|
18655 |
112399 |
EGLN3 |
14 |
34510338 |
34510338 |
Cockayne syndrome
|
HiSeq X Ten
|
27833 |
112399 |
EGLN3 |
14 |
34530036 |
34530036 |
Asymptomatic
|
HiSeq X Ten
Single cell Sequencing Cell cloning
|