ggaS0001000059817
|
chr1:12538408
|
C |
T |
intron_variant|MODIFIER
|
ENSGALG00000028239
|
G
|
downstream_gene_variant|MODIFIER |
ENSGALG00000008312
(GSAP)
|
ggaS0001000059818
|
chr1:12538501
|
T |
C |
missense_variant|MODERATE
|
ENSGALG00000028239
|
G
|
ggaS0001000059819
|
chr1:12538783
|
G |
A |
upstream_gene_variant|MODIFIER
|
ENSGALG00000028239
|
G
|
ggaS0001000059820
|
chr1:12538965
|
T |
A |
upstream_gene_variant|MODIFIER
|
ENSGALG00000028239
|
G
|
ggaS0001000059821
|
chr1:12539208
|
A |
G |
upstream_gene_variant|MODIFIER
|
ENSGALG00000028239
|
G
|
ggaS0001000059822
|
chr1:12539210
|
G |
A |
upstream_gene_variant|MODIFIER
|
ENSGALG00000028239
|
G
|
ggaS0001000059823
|
chr1:12539272
|
G |
A |
upstream_gene_variant|MODIFIER
|
ENSGALG00000028239
|
G
|
ggaS0001000059824
|
chr1:12539325
|
G |
T |
upstream_gene_variant|MODIFIER
|
ENSGALG00000028239
|
G
|
ggaS0001000059825
|
chr1:12539353
|
T |
G |
upstream_gene_variant|MODIFIER
|
ENSGALG00000028239
|
G
|
ggaS0001000059826
|
chr1:12539539
|
C |
T |
upstream_gene_variant|MODIFIER
|
ENSGALG00000028239
|
G
|