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
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
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
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Adipose_Subcutaneous
12.017
0.156
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.326
396
463
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T 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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.320
322
374
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Adrenal_Gland
4.569
0.219
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.325
163
192
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Breast_Mammary_Tissue
6.160
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.323
279
330
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
NIN
Colon_Transverse
5.231
-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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
ABHD12B
Colon_Transverse
12.791
-0.391
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Colon_Transverse
17.098
-0.456
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
NIN
Esophagus_Mucosa
36.089
-0.441
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
334
392
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
ABHD12B
Esophagus_Mucosa
18.743
-0.432
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
334
392
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Esophagus_Mucosa
32.848
-0.413
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
334
392
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Heart_Left_Ventricle
8.301
0.193
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.312
242
281
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T 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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.306
315
368
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T 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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.320
410
480
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T 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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.341
159
189
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T 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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.341
159
189
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
ABHD12B
Whole_Blood
5.143
-0.110
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.314
432
503
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Whole_Blood
9.407
0.074
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 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.314
432
503
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Adipose_Subcutaneous
11.931
0.155
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.326
395
463
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Adipose_Visceral_Omentum
6.439
0.133
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.321
322
375
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Adrenal_Gland
4.626
0.221
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.327
163
193
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Breast_Mammary_Tissue
6.090
0.107
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.322
277
329
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
NIN
Colon_Transverse
5.231
-0.162
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
ABHD12B
Colon_Transverse
12.791
-0.391
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Colon_Transverse
17.098
-0.456
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
NIN
Esophagus_Mucosa
36.089
-0.441
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
334
392
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
ABHD12B
Esophagus_Mucosa
18.743
-0.432
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
334
392
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Esophagus_Mucosa
32.848
-0.413
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
334
392
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Heart_Left_Ventricle
8.047
0.190
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.313
242
282
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Lung
6.029
0.127
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.306
314
368
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Skin_Sun_Exposed_Lower_leg
4.160
0.131
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
408
479
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
ABHD12B
Spleen
5.854
-0.269
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.343
159
190
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Spleen
6.118
0.128
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.343
159
190
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
ABHD12B
Whole_Blood
5.232
-0.111
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.313
430
501
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Whole_Blood
9.217
0.074
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.313
430
501
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50905380:splice
50905380:variant
goto
ABHD12Bdownstream_gene_variantc.*1015del others(6): Hide
PYGL
Adipose_Subcutaneous
12.113
0.157
71330203
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(198): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(211): Hide
0.326
396
463
10
chr14_50905380_CA_C_b38
+
MODIFIER
chr14
CA
C
TogoVar
50905380:splice
50905380:variant
goto
ABHD12Bdownstream_gene_variantc.*1015del others(6): Hide
PYGL
Adipose_Visceral_Omentum
6.508
0.134
71330203
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(198): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(211): Hide
0.320
322
374
10
chr14_50905380_CA_C_b38
+
MODIFIER
chr14
CA
C
TogoVar
50905380:splice
50905380:variant
goto
ABHD12Bdownstream_gene_variantc.*1015del others(6): Hide
PYGL
Adrenal_Gland
4.643
0.221
71330203
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(198): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(211): Hide
0.325
163
192
10
chr14_50905380_CA_C_b38
+
MODIFIER
chr14
CA
C
TogoVar
50905380:splice
50905380:variant
goto
ABHD12Bdownstream_gene_variantc.*1015del others(6): Hide
PYGL
Breast_Mammary_Tissue
6.097
0.108
71330203
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(198): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(211): Hide
0.323
279
330
10
chr14_50905380_CA_C_b38
+
MODIFIER
chr14
CA
C
TogoVar
50905380:splice
50905380:variant
goto
ABHD12Bdownstream_gene_variantc.*1015del others(6): Hide
NIN
Colon_Transverse
5.890
-0.174
71330203
a0001 a0002 a0004 a0005 a0008 others(2): Hide