ggaS0040004473344
|
chrW:4663
|
A |
G |
downstream_gene_variant|MODIFIER
|
ENSGALG00000025736
|
G
|
ggaS0040004473345
|
chrW:7636
|
C |
T |
missense_variant|MODERATE
|
ENSGALG00000025736
|
G
|
ggaS0040004473346
|
chrW:13769
|
A |
C |
upstream_gene_variant|MODIFIER
|
ENSGALG00000025736
|
G
|
ggaS0040004473348
|
chrW:25148
|
A |
G |
intron_variant|MODIFIER
|
ENSGALG00000005785
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000025758
|
ggaS0040004473350
|
chrW:25172
|
C |
T |
intron_variant|MODIFIER
|
ENSGALG00000005785
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000025758
|
ggaS0040004473352
|
chrW:25185
|
T |
C |
intron_variant|MODIFIER
|
ENSGALG00000005785
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000025758
|
ggaS0040004473354
|
chrW:25188
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000005785
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000025758
|
ggaS0040004473355
|
chrW:34320
|
A |
G |
intron_variant|MODIFIER
|
ENSGALG00000005785
|
G
|
ggaS0040004473356
|
chrW:36793
|
C |
T |
intron_variant|MODIFIER
|
ENSGALG00000005785
|
G
|
ggaS0040004473357
|
chrW:36977
|
G |
A |
intron_variant|MODIFIER
|
ENSGALG00000005785
|
G
|