ggaS0001000337628
|
chr1:70152967
|
A |
G |
intron_variant|MODIFIER
|
ENSGALG00000014218
(PHF21B)
|
G
|
ggaS0001000337629
|
chr1:70153191
|
A |
G |
intron_variant|MODIFIER
|
ENSGALG00000014218
(PHF21B)
|
G
|
ggaS0001000337630
|
chr1:70153223
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000014218
(PHF21B)
|
G
|
ggaS0001000337631
|
chr1:70153348
|
T |
C |
intron_variant|MODIFIER
|
ENSGALG00000014218
(PHF21B)
|
G
|
ggaS0001000337632
|
chr1:70153600
|
A |
G |
intron_variant|MODIFIER
|
ENSGALG00000014218
(PHF21B)
|
G
|
ggaS0001000337633
|
chr1:70153890
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000014218
(PHF21B)
|
G
|
ggaS0001000337634
|
chr1:70153920
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000014218
(PHF21B)
|
G
|
ggaS0001000337635
|
chr1:70154124
|
C |
T |
intron_variant|MODIFIER
|
ENSGALG00000014218
(PHF21B)
|
G
|
ggaS0001000337636
|
chr1:70155008
|
C |
T |
upstream_gene_variant|MODIFIER
|
ENSGALG00000014218
(PHF21B)
|
G
|
ggaS0001000337637
|
chr1:70155337
|
G |
C |
upstream_gene_variant|MODIFIER
|
ENSGALG00000014218
(PHF21B)
|
G
|