ggaS0001000049740
|
chr1:10503892
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049741
|
chr1:10504085
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049742
|
chr1:10504135
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049743
|
chr1:10504138
|
T |
G |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049744
|
chr1:10504147
|
G |
C |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049745
|
chr1:10504214
|
A |
G |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049746
|
chr1:10504535
|
C |
T |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049747
|
chr1:10504937
|
A |
G |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049748
|
chr1:10506504
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|
ggaS0001000049749
|
chr1:10506843
|
T |
C |
intron_variant|MODIFIER
|
ENSGALG00000008461
(HGF/SF)
|
G
|