50872157:splice
50872157:variant
goto
ABHD12B5_prime_UTR_variantc.-18A>C
VCPKMT
Muscle_Skeletal
3.660
0.377
91526329
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0002c0002 others(10): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(324): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Hide
0.971
41
48
10
chr14_50872157_A_C_b38
+
MODIFIER
chr14
A
C
TogoVar
50884303:splice
50884303:variant
goto
ABHD12Bintron_variantc.487-1311T>C
TMX1
Vagina
5.122
-0.952
91635338
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(30): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(333): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Hide
0.988
3
4
10
chr14_50884303_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50883951:splice
50883951:variant
goto
ABHD12Bintron_variantc.487-1661_487-1660 others(10): Hide
TMX1
Vagina
5.122
-0.952
91635337
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(30): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(332): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Hide
0.988
3
4
10
chr14_50883951_C_CTA_b38
+
MODIFIER
chr14
C
CTA
TogoVar
50884228:splice
50884228:variant
goto
ABHD12Bintron_variantc.487-1386A>G
TMX1
Vagina
5.122
-0.952
91635337
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(30): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(332): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Hide
0.988
3
4
10
chr14_50884228_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50884471:splice
50884471:variant
goto
ABHD12Bintron_variantc.487-1143C>G
TMX1
Vagina
5.122
-0.952
91635337
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(30): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(332): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Hide
0.988
3
4
10
chr14_50884471_C_G_b38
+
MODIFIER
chr14
C
G
TogoVar
50884575:splice
50884575:variant
goto
ABHD12Bintron_variantc.487-1039C>T
TMX1
Vagina
5.122
-0.952
91635337
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(30): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(332): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Hide
0.988
3
4
10
chr14_50884575_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50884032:splice
50884032:variant
goto
ABHD12Bintron_variantc.487-1577_487-1575 others(11): Hide
TMX1
Vagina
5.654
-0.808
81429302
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0013 a0002c0002 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(24): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(297): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Hide
0.979
6
7
10
chr14_50884032_GTCA_G_b38
+
MODIFIER
chr14
GTCA
G
TogoVar
50884333:splice
50884333:variant
goto
ABHD12Bintron_variantc.487-1281C>T
TMX1
Vagina
4.903
-0.877
91634331
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(29): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(326): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Hide
0.985
4
5
10
chr14_50884333_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50883038:splice
50883038:variant
goto
ABHD12Bintron_variantc.486+1412T>C
ABHD12B
Whole_Blood
5.678
0.203
71433323
a0001 a0002 a0003 a0004 a0007 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(28): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(318): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Hide
0.929
110
113
10
chr14_50883038_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50883364:splice
50883364:variant
goto
ABHD12Bintron_variantc.486+1738T>C
ABHD12B
Whole_Blood
5.715
0.201
61332321
a0001 a0002 a0003 a0004 a0007 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(27): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(316): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Hide
0.927
113
117
10
chr14_50883364_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50882876:splice
50882876:variant
goto
ABHD12Bintron_variantc.486+1250T>C
ABHD12B
Whole_Blood
5.849
0.203
71432319
a0001 a0002 a0003 a0004 a0007 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(27): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(314): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Hide
0.926
114
118
10
chr14_50882876_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50877047:splice
50877047:variant
goto
ABHD12Bintron_variantc.105-905G>A
ABHD12B
Whole_Blood
4.089
0.158
61331315
a0001 a0002 a0003 a0004 a0007 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(26): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(310): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Hide
0.917
127
132
10
chr14_50877047_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50882446:splice
50882446:variant
goto
ABHD12Bintron_variantc.486+820G>A
ABHD12B
Whole_Blood
5.751
0.201
71432317
a0001 a0002 a0003 a0004 a0007 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(27): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(312): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Hide
0.927
113
117
10
chr14_50882446_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50882571:splice
50882571:variant
goto
ABHD12Bintron_variantc.486+945A>G
ABHD12B
Whole_Blood
5.849
0.203
71432317
a0001 a0002 a0003 a0004 a0007 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(27): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(312): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Hide
0.926
114
118
10
chr14_50882571_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50882582:splice
50882582:variant
goto
ABHD12Bintron_variantc.486+956G>A
ABHD12B
Whole_Blood
5.849
0.203
71432317
a0001 a0002 a0003 a0004 a0007 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(27): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(312): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Hide
0.926
114
118
10
chr14_50882582_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50882616:splice
50882616:variant
goto
ABHD12Bintron_variantc.486+990G>A
ABHD12B
Whole_Blood
5.849
0.203
71432317
a0001 a0002 a0003 a0004 a0007 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(27): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(312): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Hide
0.926
114
118
10
chr14_50882616_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50882728:splice
50882728:variant
goto
ABHD12Bintron_variantc.486+1102G>A
ABHD12B
Whole_Blood
5.849
0.203
71432317
a0001 a0002 a0003 a0004 a0007 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(27): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(312): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Hide
0.926
114
118
10
chr14_50882728_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
PYGL
Artery_Tibial
7.280
-0.170
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.728
328
375
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
NIN
Colon_Transverse
5.213
0.164
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.700
254
287
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
ABHD12B
Colon_Transverse
9.078
0.332
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.700
254
287
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
PYGL
Colon_Transverse
7.730
0.309
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.700
254
287
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
NIN
Esophagus_Mucosa
32.493
0.453
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.731
297
330
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
ABHD12B
Esophagus_Mucosa
13.038
0.389
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.731
297
330
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
PYGL
Esophagus_Mucosa
32.638
0.443
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.731
297
330
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
PYGL
Skin_Not_Sun_Exposed_Suprapubic
4.800
-0.144
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.720
318
364
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
PYGL
Skin_Sun_Exposed_Lower_leg
6.494
-0.169
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.719
365
422
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
ABHD12B
Whole_Blood
4.742
0.108
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.729
382
434
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50880305:splice
50880305:variant
goto
ABHD12Bintron_variantc.336-147T>C
ABHD12B
Whole_Blood
4.209
0.155
51021274
a0001 a0002 a0003 a0004 a0007
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(5): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(16): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(269): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Hide
0.907
139
149
10
chr14_50880305_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50888444:splice
50888444:variant
goto
ABHD12Bintron_variantc.701-380C>T
PYGL
Esophagus_Mucosa
3.714
0.183
5616265
a0001 a0002 a0003 a0004 a0007
a0001c0001 a0001c0005 a0002c0002 a0003c0003 a0004c0007 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(11): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(260): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Hide
0.870
145
160
10
chr14_50888444_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50888444:splice
50888444:variant
goto
ABHD12Bintron_variantc.701-380C>T
ABHD12B
Whole_Blood
4.266
0.127
5616265
a0001 a0002 a0003 a0004 a0007
a0001c0001 a0001c0005 a0002c0002 a0003c0003 a0004c0007 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(11): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(260): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Hide
0.866
191
214
10
chr14_50888444_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50871519:splice
50871519:variant
goto
ABHD12Bupstream_gene_variantc.-656A>Gothers(2): Hide
ABHD12B
Colon_Transverse
4.922
0.325
81427252
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0002c0002 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0016 a0001c0005t0004 others(22): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0018 others(247): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Hide
0.865
116
129
10
chr14_50871519_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50874460:splice
50874460:variant
goto
ABHD12Bintron_variantc.104+2182C>A
ABHD12B
Brain_Caudate_basal_ganglia
8.787
0.189
5101499
a0001 a0002 a0003 a0004 a0005
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0002c0002 others(5): Hide
a0001c0001t0001 a0001c0001t0016 a0001c0005t0007 a0001c0006t0001 a0001c0011t0004 others(9): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0038 others(94): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp2 HG00438.hp1 HG00438.hp2 others(102): Hide
0.356
168
212
10
chr14_50874460_C_A_b38
+
MODIFIER
chr14
C
A
TogoVar
50874460:splice
50874460:variant
goto
ABHD12Bintron_variantc.104+2182C>A
ABHD12B
Brain_Nucleus_accumbens_basal_ganglia
5.589
0.185
5101499
a0001 a0002 a0003 a0004 a0005
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0002c0002 others(5): Hide
a0001c0001t0001 a0001c0001t0016 a0001c0005t0007 a0001c0006t0001 a0001c0011t0004 others(9): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0038 others(94): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp2 HG00438.hp1 HG00438.hp2 others(102): Hide
0.373
167
212
10
chr14_50874460_C_A_b38
+
MODIFIER
chr14
C
A
TogoVar
50874460:splice
50874460:variant
goto
ABHD12Bintron_variantc.104+2182C>A
ABHD12B
Thyroid
7.448
0.292
5101499
a0001 a0002 a0003 a0004 a0005
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0002c0002 others(5): Hide
a0001c0001t0001 a0001c0001t0016 a0001c0005t0007 a0001c0006t0001 a0001c0011t0004 others(9): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0038 others(94): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp2 HG00438.hp1 HG00438.hp2 others(102): Hide
0.352
388
480
10
chr14_50874460_C_A_b38
+
MODIFIER
chr14
C
A
TogoVar
50868534:splice
50868534:variant
goto
ABHD12Bupstream_gene_variantc.-3641G>A others(3): Hide
ABHD12B
Brain_Caudate_basal_ganglia
14.807
-0.260
7121987
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(14): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0032 others(82): Hide
HG00099.hp1 HG00408.hp2 HG00438.hp2 HG00544.hp1 HG00558.hp2 others(87): Hide
0.304
153
181
10
chr14_50868534_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50868562:splice
50868562:variant
goto
ABHD12Bupstream_gene_variantc.-3613G>A others(3): Hide
ABHD12B
Brain_Caudate_basal_ganglia
14.807
-0.260
7121987
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(14): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0032 others(82): Hide
HG00099.hp1 HG00408.hp2 HG00438.hp2 HG00544.hp1 HG00558.hp2 others(87): Hide
0.304
153
181
10
chr14_50868562_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50868534:splice
50868534:variant
goto
ABHD12Bupstream_gene_variantc.-3641G>A others(3): Hide
ABHD12B
Brain_Nucleus_accumbens_basal_ganglia
13.640
-0.294
7121987
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(14): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0032 others(82): Hide
HG00099.hp1 HG00408.hp2 HG00438.hp2 HG00544.hp1 HG00558.hp2 others(87): Hide
0.301
144
171
10
chr14_50868534_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50868562:splice
50868562:variant
goto
ABHD12Bupstream_gene_variantc.-3613G>A others(3): Hide
ABHD12B
Brain_Nucleus_accumbens_basal_ganglia
13.640
-0.294
7121987
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(14): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0032 others(82): Hide
HG00099.hp1 HG00408.hp2 HG00438.hp2 HG00544.hp1 HG00558.hp2 others(87): Hide
0.301
144
171
10
chr14_50868562_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50868534:splice
50868534:variant
goto
ABHD12Bupstream_gene_variantc.-3641G>A others(3): Hide
ABHD12B
Brain_Putamen_basal_ganglia
4.400
-0.139
7121987
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(14): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0032 others(82): Hide
HG00099.hp1 HG00408.hp2 HG00438.hp2 HG00544.hp1 HG00558.hp2 others(87): Hide
0.300
127
152
10
chr14_50868534_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50868562:splice
50868562:variant
goto
ABHD12Bupstream_gene_variantc.-3613G>A others(3): Hide
ABHD12B
Brain_Putamen_basal_ganglia
4.400
-0.139
7121987
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(14): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0032 others(82): Hide
HG00099.hp1 HG00408.hp2 HG00438.hp2 HG00544.hp1 HG00558.hp2 others(87): Hide
0.300
127
152
10
chr14_50868562_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50888799:splice
50888799:variant
goto
ABHD12Bintron_variantc.701-25C>A
PYGL
Esophagus_Mucosa
5.765
0.168
4819197
a0001 a0002 a0003 a0004
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(14): Hide
a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(192): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00438.hp1 others(204): Hide
0.696
313
373
10
chr14_50888799_C_A_b38
+
MODIFIER
chr14
C
A
TogoVar
50868217:splice
50868217:variant
goto
ABHD12Bupstream_gene_variantc.-3958G>A others(3): Hide
ABHD12B
Brain_Caudate_basal_ganglia
14.920
-0.261
6111444
a0001 a0002 a0003 a0004 a0005 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0006t0001 a0002c0002t0002 others(9): Hide
a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0160 a0001c0001t0001g0180 others(39): Hide
HG00099.hp1 HG00642.hp1 HG01099.hp1 HG01106.hp2 HG01167.hp2 others(43): Hide
0.299
150
178
10
chr14_50868217_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50868217:splice
50868217:variant
goto
ABHD12Bupstream_gene_variantc.-3958G>A others(3): Hide
ABHD12B
Brain_Nucleus_accumbens_basal_ganglia
13.163
-0.290
6111444
a0001 a0002 a0003 a0004 a0005 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0006t0001 a0002c0002t0002 others(9): Hide
a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0160 a0001c0001t0001g0180 others(39): Hide
HG00099.hp1 HG00642.hp1 HG01099.hp1 HG01106.hp2 HG01167.hp2 others(43): Hide
0.294
140
167
10
chr14_50868217_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50868217:splice
50868217:variant
goto
ABHD12Bupstream_gene_variantc.-3958G>A others(3): Hide
ABHD12B
Brain_Putamen_basal_ganglia
4.578
-0.142
6111444
a0001 a0002 a0003 a0004 a0005 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0006t0001 a0002c0002t0002 others(9): Hide
a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0160 a0001c0001t0001g0180 others(39): Hide
HG00099.hp1 HG00642.hp1 HG01099.hp1 HG01106.hp2 HG01167.hp2 others(43): Hide
0.298
126
151
10
chr14_50868217_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50869179:splice
50869179:variant
goto
ABHD12Bupstream_gene_variantc.-2996C>A others(3): Hide
ABHD12B
Thyroid
5.388
-0.240
81418130
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(13): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(125): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(133): Hide
0.385
428
524
10
chr14_50869179_C_A_b38
+
MODIFIER
chr14
C
A
TogoVar
50869019:splice
50869019:variant
goto
ABHD12Bupstream_gene_variantc.-3156T>C others(3): Hide
VCPKMT
Skin_Not_Sun_Exposed_Suprapubic
4.150
0.092
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.371
392
482
10
chr14_50869019_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50869025:splice
50869025:variant
goto
ABHD12Bupstream_gene_variantc.-3150G>A others(3): Hide
VCPKMT
Skin_Not_Sun_Exposed_Suprapubic
4.150
0.092
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.371
392
482
10
chr14_50869025_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50869019:splice
50869019:variant
goto
ABHD12Bupstream_gene_variantc.-3156T>C others(3): Hide
NIN
Thyroid
3.960
-0.102
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.375
418
511
10
chr14_50869019_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50869025:splice
50869025:variant
goto
ABHD12Bupstream_gene_variantc.-3150G>A others(3): Hide
NIN
Thyroid
3.759
-0.100
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.374
418
510
10
chr14_50869025_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50869019:splice
50869019:variant
goto
ABHD12Bupstream_gene_variantc.-3156T>C others(3): Hide
ABHD12B
Thyroid
6.107
-0.259
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.375
418
511
10
chr14_50869019_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50869025:splice
50869025:variant
goto
ABHD12Bupstream_gene_variantc.-3150G>A others(3): Hide
ABHD12B
Thyroid
6.056
-0.258
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.374
418
510
10
chr14_50869025_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50870432:splice
50870432:variant
goto
ABHD12Bupstream_gene_variantc.-1743G>A others(3): Hide
ABHD12B
Brain_Nucleus_accumbens_basal_ganglia
4.408
0.193
71316110
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(11): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(105): Hide
HG00140.hp1 HG00408.hp1 HG00423.hp1 HG00423.hp2 HG00544.hp2 others(113): Hide
0.199
104
113
10
chr14_50870432_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50870751:splice
50870751:variant
goto
ABHD12Bupstream_gene_variantc.-1424G>A others(3): Hide
ABHD12B
Brain_Nucleus_accumbens_basal_ganglia
4.904
0.204
61215113
a0001 a0002 a0003 a0004 a0005 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0081 others(108): Hide
HG00140.hp1 HG00408.hp1 HG00423.hp1 HG00423.hp2 HG00544.hp2 others(118): Hide
0.222
115
126
10
chr14_50870751_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50870751:splice
50870751:variant
goto
ABHD12Bupstream_gene_variantc.-1424G>A others(3): Hide
SAV1
Cells_Cultured_fibroblasts
4.011
0.112
61215113
a0001 a0002 a0003 a0004 a0005 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0081 others(108): Hide
HG00140.hp1 HG00408.hp1 HG00423.hp1 HG00423.hp2 HG00544.hp2 others(118): Hide
0.230
267
298
10
chr14_50870751_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50870751:splice
50870751:variant
goto
ABHD12Bupstream_gene_variantc.-1424G>A others(3): Hide
VCPKMT
Skin_Sun_Exposed_Lower_leg
4.337
-0.116
61215113
a0001 a0002 a0003 a0004 a0005 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0081 others(108): Hide
HG00140.hp1 HG00408.hp1 HG00423.hp1 HG00423.hp2 HG00544.hp2 others(118): Hide
0.225
304
338
10
chr14_50870751_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50874372:splice
50874372:variant
goto
ABHD12Bintron_variantc.104+2094G>A
ABHD12B
Thyroid
3.915
-0.228
7101278
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(5): Hide
a0001c0001t0001 a0001c0005t0004 a0001c0006t0001 a0002c0002t0002 a0002c0002t0005 others(7): Hide
a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0233 others(73): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00423.hp1 HG00423.hp2 others(77): Hide
0.239
283
326
10
chr14_50874372_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Artery_Tibial
4.327
-0.182
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.128
159
177
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Cells_Cultured_fibroblasts
4.687
0.164
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.126
144
163
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Esophagus_Mucosa
6.164
0.270
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.126
138
155
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Esophagus_Muscularis
6.315
-0.210
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.127
128
143
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
ABHD12B
Nerve_Tibial
5.580
0.342
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.127
152
170
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Stomach
5.650
-0.194
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.144
102
117
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Thyroid
4.738
-0.186
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.131
160
179
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Adipose_Subcutaneous
12.185
0.158
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.325
395
462
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Adipose_Visceral_Omentum
6.477
0.134
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.320
322
374
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Adrenal_Gland
4.746
0.224
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.324
162
191
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Breast_Mammary_Tissue
5.988
0.107
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.322
278
329
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
NIN
Colon_Transverse
5.213
-0.162
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.331
269
316
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
ABHD12B
Colon_Transverse
12.554
-0.387
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.331
269
316
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Colon_Transverse
17.051
-0.455
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.331
269
316
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
NIN
Esophagus_Mucosa
35.494
-0.437
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.318
333
391
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
ABHD12B
Esophagus_Mucosa
18.330
-0.427
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.318
333
391
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Esophagus_Mucosa
32.099
-0.408
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.318
333
391
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Heart_Left_Ventricle
8.605
0.196
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.311
241
280
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Lung
6.171
0.129
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.306
315
368
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Skin_Sun_Exposed_Lower_leg
4.151
0.131
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.320
410
480
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
ABHD12B
Spleen
5.943
-0.271
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.341
159
189
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Spleen
6.144
0.129
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.341
159
189
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
ABHD12B
Whole_Blood
5.042
-0.108
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.314
431
502
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Whole_Blood
9.706
0.076
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.314
431
502
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Adipose_Subcutaneous
8.907
0.145
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.238
306
339
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Adipose_Visceral_Omentum
4.964
0.127
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide