Variants
Found 8 variants in this database.
Variant ID |
Entrez Gene ID |
Gene |
Chromsome |
Start |
End |
Disease |
Method |
1666 |
55733 |
HHAT |
1 |
210625900 |
210625900 |
Asymptomatic
|
HiSeq X Ten
|
1774 |
55733 |
HHAT |
1 |
210505477 |
210505477 |
Asymptomatic
|
HiSeq X Ten
|
2121 |
55733 |
HHAT |
1 |
210649221 |
210649221 |
Asymptomatic
|
HiSeq X Ten
|
2296 |
55733 |
HHAT |
1 |
210522496 |
210522496 |
Asymptomatic
|
HiSeq X Ten
|
2524 |
55733 |
HHAT |
1 |
210790449 |
210790449 |
Asymptomatic
|
HiSeq X Ten
|
2570 |
55733 |
HHAT |
1 |
210817850 |
210817850 |
Asymptomatic
|
HiSeq X Ten
|
2722 |
55733 |
HHAT |
1 |
210586015 |
210586015 |
Cockayne syndrome
|
HiSeq X Ten
|
24555 |
55733 |
HHAT |
1 |
210785378 |
210785378 |
Asymptomatic
|
HiSeq X Ten
Single cell Sequencing Cell cloning
|