ggaS0048001477884
|
chr16:1221
|
G |
T |
upstream_gene_variant|MODIFIER
|
ENSGALG00000027865
(CD1.2)
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000012494
(CD1A1)
|
ggaS0048001477887
|
chr16:1362
|
G |
A |
upstream_gene_variant|MODIFIER
|
ENSGALG00000027865
(CD1.2)
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000012494
(CD1A1)
|
ggaS0048001477890
|
chr16:1685
|
T |
C |
upstream_gene_variant|MODIFIER
|
ENSGALG00000027865
(CD1.2)
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000012494
(CD1A1)
|
ggaS0048001477893
|
chr16:2029
|
G |
A |
upstream_gene_variant|MODIFIER
|
ENSGALG00000027865
(CD1.2)
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000012494
(CD1A1)
|
ggaS0048001477896
|
chr16:2798
|
G |
A |
upstream_gene_variant|MODIFIER
|
ENSGALG00000027865
(CD1.2)
|
G
|
intron_variant|MODIFIER |
ENSGALG00000012494
(CD1A1)
|
ggaS0048001477899
|
chr16:3127
|
A |
G |
upstream_gene_variant|MODIFIER
|
ENSGALG00000027865
(CD1.2)
|
G
|
intron_variant|MODIFIER |
ENSGALG00000012494
(CD1A1)
|
ggaS0048001477902
|
chr16:4117
|
G |
A |
upstream_gene_variant|MODIFIER
|
ENSGALG00000027865
(CD1.2)
|
G
|
missense_variant|MODERATE; intron_variant|MODIFIER |
ENSGALG00000012494
(CD1A1)
|
ggaS0048001477906
|
chr16:4826
|
C |
T |
downstream_gene_variant|MODIFIER
|
ENSGALG00000019831
(LTB4R2)
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000027865
(CD1.2)
|
3_prime_UTR_variant|MODIFIER |
ENSGALG00000012494
(CD1A1)
|
ggaS0048001477910
|
chr16:5155
|
A |
G |
downstream_gene_variant|MODIFIER
|
ENSGALG00000019831
(LTB4R2)
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000027865
(CD1.2)
|
downstream_gene_variant|MODIFIER |
ENSGALG00000012494
(CD1A1)
|
ggaS0048001477914
|
chr16:5547
|
T |
C |
downstream_gene_variant|MODIFIER
|
ENSGALG00000019831
(LTB4R2)
|
G
|
upstream_gene_variant|MODIFIER |
ENSGALG00000027865
(CD1.2)
|
downstream_gene_variant|MODIFIER |
ENSGALG00000012494
(CD1A1)
|