ggaS0001000049730
|
chr1:10501602
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049731
|
chr1:10501619
|
C |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049732
|
chr1:10501634
|
A |
C |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049733
|
chr1:10502181
|
A |
G |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049734
|
chr1:10502214
|
C |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049735
|
chr1:10502345
|
T |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049736
|
chr1:10502794
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049737
|
chr1:10503185
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049738
|
chr1:10503261
|
A |
G |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049739
|
chr1:10503863
|
T |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|