112089263:splice
112089263:variant
goto
C3orf52intron_variantc.138+2718C>T
C3orf52
Skin_Sun_Exposed_Lower_leg
4.318
0.120
4824173
a0001 a0007 a0008 a0009
a0001c0001 a0001c0004 a0001c0011 a0001c0012 a0001c0013 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(19): Hide
a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(168): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00280.hp2 others(298): Hide
0.910
110
135
10
chr3_112089263_C_T_b38
+
MODIFIER
chr3
C
T
TogoVar
112089263:splice
112089263:variant
goto
C3orf52intron_variantc.138+2718C>T
GCSAM
Whole_Blood
3.732
0.153
4824173
a0001 a0007 a0008 a0009
a0001c0001 a0001c0004 a0001c0011 a0001c0012 a0001c0013 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(19): Hide
a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(168): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00280.hp2 others(298): Hide
0.903
126
155
10
chr3_112089263_C_T_b38
+
MODIFIER
chr3
C
T
TogoVar
112088872:splice
112088872:variant
goto
C3orf52intron_variantc.138+2327G>A
TMPRSS7
Skin_Sun_Exposed_Lower_leg
3.675
0.173
4619118
a0001 a0007 a0008 a0009
a0001c0001 a0001c0004 a0001c0013 a0007c0009 a0008c0010 others(1): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(14): Hide
a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(113): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Hide
0.780
269
330
10
chr3_112088872_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112088872:splice
112088872:variant
goto
C3orf52intron_variantc.138+2327G>A
SLC9C1
Testis
5.299
-0.218
4619118
a0001 a0007 a0008 a0009
a0001c0001 a0001c0004 a0001c0013 a0007c0009 a0008c0010 others(1): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(14): Hide
a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(113): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Hide
0.792
145
172
10
chr3_112088872_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112088872:splice
112088872:variant
goto
C3orf52intron_variantc.138+2327G>A
SLC9C1
Thyroid
3.754
0.138
4619118
a0001 a0007 a0008 a0009
a0001c0001 a0001c0004 a0001c0013 a0007c0009 a0008c0010 others(1): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(14): Hide
a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(113): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Hide
0.791
231
284
10
chr3_112088872_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
C3orf52
Cells_Cultured_fibroblasts
4.797
0.095
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.419
427
544
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
GCSAM
Cells_EBV-transformed_lymphocytes
4.839
0.127
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.445
220
290
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
SLC9C1
Heart_Left_Ventricle
4.639
0.150
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.428
298
385
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
GCSAM
Lung
4.124
0.098
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.418
392
502
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
C3orf52
Pancreas
11.002
0.271
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.401
228
290
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
GCSAM
Pancreas
10.875
0.284
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.401
228
290
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
SLC9C1
Pancreas
5.799
0.228
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.401
228
290
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
TMPRSS7
Skin_Sun_Exposed_Lower_leg
3.705
-0.133
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.421
494
633
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
TMPRSS7
Testis
6.749
-0.144
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.391
255
323
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
C3orf52
Testis
10.149
-0.194
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.391
255
323
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
GCSAM
Testis
4.914
-0.225
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.391
255
323
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112109537:splice
112109537:variant
goto
C3orf52splice_acceptor_variant&intron_variant others(21): Hide
SLC9C1
Testis
48.860
0.458
7918101
a0001 a0002 a0004 a0005 a0006 others(2): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0004c0005 others(4): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(96): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.391
255
323
10
chr3_112109537_G_GT_b38
+
HIGH
chr3
G
GT
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
C3orf52
Cells_Cultured_fibroblasts
5.253
0.101
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.417
426
541
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
GCSAM
Cells_EBV-transformed_lymphocytes
4.748
0.126
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.439
219
286
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
SLC9C1
Heart_Left_Ventricle
4.426
0.146
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.426
298
383
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
GCSAM
Lung
4.164
0.099
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.416
392
500
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
C3orf52
Pancreas
11.754
0.281
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.398
228
288
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
GCSAM
Pancreas
11.357
0.291
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.398
228
288
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
SLC9C1
Pancreas
5.820
0.229
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.398
228
288
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
TMPRSS7
Skin_Sun_Exposed_Lower_leg
3.547
-0.130
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.419
494
630
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
TMPRSS7
Testis
6.459
-0.141
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.389
255
321
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
C3orf52
Testis
9.765
-0.191
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.389
255
321
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
GCSAM
Testis
4.654
-0.219
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.389
255
321
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112105225:splice
112105225:variant
goto
C3orf52intron_variantc.396+2260T>C
SLC9C1
Testis
51.569
0.468
6817100
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(12): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(95): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(149): Hide
0.389
255
321
10
chr3_112105225_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar
112109629:splice
112109629:variant
goto
C3orf52intron_variantc.467+16A>G
SLC9C1
Esophagus_Muscularis
4.099
0.189
351171
a0001 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(6): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(66): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(110): Hide
0.345
319
387
10
chr3_112109629_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112109629:splice
112109629:variant
goto
C3orf52intron_variantc.467+16A>G
CD200
Nerve_Tibial
5.176
0.102
351171
a0001 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(6): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(66): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(110): Hide
0.351
379
468
10
chr3_112109629_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112109629:splice
112109629:variant
goto
C3orf52intron_variantc.467+16A>G
C3orf52
Pancreas
13.883
0.313
351171
a0001 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(6): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(66): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(110): Hide
0.327
195
237
10
chr3_112109629_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112109629:splice
112109629:variant
goto
C3orf52intron_variantc.467+16A>G
GCSAM
Pancreas
14.962
0.342
351171
a0001 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(6): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(66): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(110): Hide
0.327
195
237
10
chr3_112109629_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112109629:splice
112109629:variant
goto
C3orf52intron_variantc.467+16A>G
SLC9C1
Pancreas
6.556
0.251
351171
a0001 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(6): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(66): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(110): Hide
0.327
195
237
10
chr3_112109629_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112109629:splice
112109629:variant
goto
C3orf52intron_variantc.467+16A>G
TMPRSS7
Skin_Sun_Exposed_Lower_leg
3.595
-0.133
351171
a0001 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(6): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(66): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(110): Hide
0.352
432
529
10
chr3_112109629_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112109629:splice
112109629:variant
goto
C3orf52intron_variantc.467+16A>G
TMPRSS7
Testis
8.440
-0.168
351171
a0001 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(6): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(66): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(110): Hide
0.318
218
263
10
chr3_112109629_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112109629:splice
112109629:variant
goto
C3orf52intron_variantc.467+16A>G
C3orf52
Testis
7.835
-0.176
351171
a0001 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(6): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(66): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(110): Hide
0.318
218
263
10
chr3_112109629_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112109629:splice
112109629:variant
goto
C3orf52intron_variantc.467+16A>G
GCSAM
Testis
5.544
-0.249
351171
a0001 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(6): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(66): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(110): Hide
0.318
218
263
10
chr3_112109629_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112109629:splice
112109629:variant
goto
C3orf52intron_variantc.467+16A>G
SLC9C1
Testis
45.944
0.464
351171
a0001 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(6): Hide
a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(66): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(110): Hide
0.318
218
263
10
chr3_112109629_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112088091:splice
112088091:variant
goto
C3orf52intron_variantc.138+1546G>C
CD200
Nerve_Tibial
4.607
0.116
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.212
252
283
10
chr3_112088091_G_C_b38
+
MODIFIER
chr3
G
C
TogoVar
112089895:splice
112089895:variant
goto
C3orf52intron_variantc.138+3350T>G
CD200
Nerve_Tibial
4.607
0.116
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.212
252
283
10
chr3_112089895_T_G_b38
+
MODIFIER
chr3
T
G
TogoVar
112091155:splice
112091155:variant
goto
C3orf52intron_variantc.139-2205C>T
CD200
Nerve_Tibial
4.607
0.116
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.212
252
283
10
chr3_112091155_C_T_b38
+
MODIFIER
chr3
C
T
TogoVar
112100923:splice
112100923:variant
goto
C3orf52intron_variantc.269-1915A>G
CD200
Nerve_Tibial
4.607
0.116
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.212
252
283
10
chr3_112100923_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112088091:splice
112088091:variant
goto
C3orf52intron_variantc.138+1546G>C
C3orf52
Pancreas
30.602
0.524
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112088091_G_C_b38
+
MODIFIER
chr3
G
C
TogoVar
112089895:splice
112089895:variant
goto
C3orf52intron_variantc.138+3350T>G
C3orf52
Pancreas
30.602
0.524
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112089895_T_G_b38
+
MODIFIER
chr3
T
G
TogoVar
112091155:splice
112091155:variant
goto
C3orf52intron_variantc.139-2205C>T
C3orf52
Pancreas
30.602
0.524
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112091155_C_T_b38
+
MODIFIER
chr3
C
T
TogoVar
112100923:splice
112100923:variant
goto
C3orf52intron_variantc.269-1915A>G
C3orf52
Pancreas
30.602
0.524
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112100923_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112088091:splice
112088091:variant
goto
C3orf52intron_variantc.138+1546G>C
GCSAM
Pancreas
28.778
0.539
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112088091_G_C_b38
+
MODIFIER
chr3
G
C
TogoVar
112089895:splice
112089895:variant
goto
C3orf52intron_variantc.138+3350T>G
GCSAM
Pancreas
28.778
0.539
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112089895_T_G_b38
+
MODIFIER
chr3
T
G
TogoVar
112091155:splice
112091155:variant
goto
C3orf52intron_variantc.139-2205C>T
GCSAM
Pancreas
28.778
0.539
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112091155_C_T_b38
+
MODIFIER
chr3
C
T
TogoVar
112100923:splice
112100923:variant
goto
C3orf52intron_variantc.269-1915A>G
GCSAM
Pancreas
28.778
0.539
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112100923_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112088091:splice
112088091:variant
goto
C3orf52intron_variantc.138+1546G>C
SLC9C1
Pancreas
19.821
0.510
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112088091_G_C_b38
+
MODIFIER
chr3
G
C
TogoVar
112089895:splice
112089895:variant
goto
C3orf52intron_variantc.138+3350T>G
SLC9C1
Pancreas
19.821
0.510
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112089895_T_G_b38
+
MODIFIER
chr3
T
G
TogoVar
112091155:splice
112091155:variant
goto
C3orf52intron_variantc.139-2205C>T
SLC9C1
Pancreas
19.821
0.510
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112091155_C_T_b38
+
MODIFIER
chr3
C
T
TogoVar
112100923:splice
112100923:variant
goto
C3orf52intron_variantc.269-1915A>G
SLC9C1
Pancreas
19.821
0.510
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.203
129
147
10
chr3_112100923_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112088091:splice
112088091:variant
goto
C3orf52intron_variantc.138+1546G>C
TMPRSS7
Testis
8.051
-0.191
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112088091_G_C_b38
+
MODIFIER
chr3
G
C
TogoVar
112089895:splice
112089895:variant
goto
C3orf52intron_variantc.138+3350T>G
TMPRSS7
Testis
8.051
-0.191
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112089895_T_G_b38
+
MODIFIER
chr3
T
G
TogoVar
112091155:splice
112091155:variant
goto
C3orf52intron_variantc.139-2205C>T
TMPRSS7
Testis
8.051
-0.191
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112091155_C_T_b38
+
MODIFIER
chr3
C
T
TogoVar
112100923:splice
112100923:variant
goto
C3orf52intron_variantc.269-1915A>G
TMPRSS7
Testis
8.051
-0.191
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112100923_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112088091:splice
112088091:variant
goto
C3orf52intron_variantc.138+1546G>C
C3orf52
Testis
13.611
-0.270
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112088091_G_C_b38
+
MODIFIER
chr3
G
C
TogoVar
112089895:splice
112089895:variant
goto
C3orf52intron_variantc.138+3350T>G
C3orf52
Testis
13.611
-0.270
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112089895_T_G_b38
+
MODIFIER
chr3
T
G
TogoVar
112091155:splice
112091155:variant
goto
C3orf52intron_variantc.139-2205C>T
C3orf52
Testis
13.611
-0.270
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112091155_C_T_b38
+
MODIFIER
chr3
C
T
TogoVar
112100923:splice
112100923:variant
goto
C3orf52intron_variantc.269-1915A>G
C3orf52
Testis
13.611
-0.270
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112100923_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112088091:splice
112088091:variant
goto
C3orf52intron_variantc.138+1546G>C
GCSAM
Testis
7.037
-0.329
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112088091_G_C_b38
+
MODIFIER
chr3
G
C
TogoVar
112089895:splice
112089895:variant
goto
C3orf52intron_variantc.138+3350T>G
GCSAM
Testis
7.037
-0.329
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112089895_T_G_b38
+
MODIFIER
chr3
T
G
TogoVar
112091155:splice
112091155:variant
goto
C3orf52intron_variantc.139-2205C>T
GCSAM
Testis
7.037
-0.329
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112091155_C_T_b38
+
MODIFIER
chr3
C
T
TogoVar
112100923:splice
112100923:variant
goto
C3orf52intron_variantc.269-1915A>G
GCSAM
Testis
7.037
-0.329
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112100923_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112088091:splice
112088091:variant
goto
C3orf52intron_variantc.138+1546G>C
SLC9C1
Testis
31.792
0.467
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112088091_G_C_b38
+
MODIFIER
chr3
G
C
TogoVar
112089895:splice
112089895:variant
goto
C3orf52intron_variantc.138+3350T>G
SLC9C1
Testis
31.792
0.467
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112089895_T_G_b38
+
MODIFIER
chr3
T
G
TogoVar
112091155:splice
112091155:variant
goto
C3orf52intron_variantc.139-2205C>T
SLC9C1
Testis
31.792
0.467
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112091155_C_T_b38
+
MODIFIER
chr3
C
T
TogoVar
112100923:splice
112100923:variant
goto
C3orf52intron_variantc.269-1915A>G
SLC9C1
Testis
31.792
0.467
33613
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(18): Hide
0.201
147
166
10
chr3_112100923_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112084933:splice
112084933:variant
goto
C3orf52upstream_gene_variantc.-1475A>G others(3): Hide
C3orf52
Pancreas
20.235
0.502
33612
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(7): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(17): Hide
0.160
108
116
10
chr3_112084933_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112084933:splice
112084933:variant
goto
C3orf52upstream_gene_variantc.-1475A>G others(3): Hide
GCSAM
Pancreas
16.343
0.480
33612
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(7): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(17): Hide
0.160
108
116
10
chr3_112084933_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112084933:splice
112084933:variant
goto
C3orf52upstream_gene_variantc.-1475A>G others(3): Hide
SLC9C1
Pancreas
9.889
0.418
33612
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(7): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(17): Hide
0.160
108
116
10
chr3_112084933_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112084933:splice
112084933:variant
goto
C3orf52upstream_gene_variantc.-1475A>G others(3): Hide
TMPRSS7
Testis
4.324
-0.153
33612
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(7): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(17): Hide
0.153
114
126
10
chr3_112084933_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112084933:splice
112084933:variant
goto
C3orf52upstream_gene_variantc.-1475A>G others(3): Hide
C3orf52
Testis
8.409
-0.238
33612
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(7): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(17): Hide
0.153
114
126
10
chr3_112084933_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112084933:splice
112084933:variant
goto
C3orf52upstream_gene_variantc.-1475A>G others(3): Hide
GCSAM
Testis
4.713
-0.297
33612
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(7): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(17): Hide
0.153
114
126
10
chr3_112084933_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112084933:splice
112084933:variant
goto
C3orf52upstream_gene_variantc.-1475A>G others(3): Hide
SLC9C1
Testis
19.643
0.423
33612
a0001 a0008 a0009
a0001c0001 a0008c0010 a0009c0008
a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 a0008c0010t0002 others(1): Hide
a0001c0001t0001g0067 a0001c0001t0002g0004 a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(7): Hide
HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00738.hp2 HG01069.hp2 others(17): Hide
0.153
114
126
10
chr3_112084933_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
C3orf52
Cells_Cultured_fibroblasts
5.438
0.100
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.419
421
544
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
GCSAM
Cells_EBV-transformed_lymphocytes
4.213
0.119
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.440
220
287
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
SLC9C1
Heart_Left_Ventricle
5.387
0.162
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.422
294
380
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
GCSAM
Lung
4.473
0.102
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.421
392
506
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
C3orf52
Pancreas
12.276
0.285
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.394
225
285
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
GCSAM
Pancreas
12.033
0.297
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.394
225
285
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
SLC9C1
Pancreas
6.276
0.237
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.394
225
285
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
TMPRSS7
Testis
6.160
-0.139
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.390
257
322
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
C3orf52
Testis
9.804
-0.193
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.390
257
322
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
GCSAM
Testis
4.994
-0.230
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.390
257
322
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
SLC9C1
Testis
51.774
0.474
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.390
257
322
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112113273:splice
112113273:variant
goto
C3orf52intron_variantc.649+128A>G
PHLDB2
Thyroid
3.849
-0.100
6816103
a0001 a0002 a0005 a0006 a0008 others(1): Hide
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0005c0006 others(3): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(98): Hide
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp1 HG00423.hp2 others(152): Hide
0.408
433
556
10
chr3_112113273_A_G_b38
+
MODIFIER
chr3
A
G
TogoVar
112115906:splice
112115906:variant
goto
C3orf52intron_variantc.650-736G>A
SLC9C1
Cells_EBV-transformed_lymphocytes
4.046
0.275
461175
a0001 a0002 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0008c0010 others(1): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(6): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(70): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(116): Hide
0.376
196
245
10
chr3_112115906_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112115906:splice
112115906:variant
goto
C3orf52intron_variantc.650-736G>A
CD200
Nerve_Tibial
4.929
0.098
461175
a0001 a0002 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0008c0010 others(1): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(6): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(70): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(116): Hide
0.369
393
492
10
chr3_112115906_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112115906:splice
112115906:variant
goto
C3orf52intron_variantc.650-736G>A
C3orf52
Pancreas
13.846
0.307
461175
a0001 a0002 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0008c0010 others(1): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(6): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(70): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(116): Hide
0.330
196
239
10
chr3_112115906_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112115906:splice
112115906:variant
goto
C3orf52intron_variantc.650-736G>A
GCSAM
Pancreas
15.027
0.337
461175
a0001 a0002 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0008c0010 others(1): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(6): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(70): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(116): Hide
0.330
196
239
10
chr3_112115906_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112115906:splice
112115906:variant
goto
C3orf52intron_variantc.650-736G>A
SLC9C1
Pancreas
7.881
0.272
461175
a0001 a0002 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0008c0010 others(1): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(6): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(70): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(116): Hide
0.330
196
239
10
chr3_112115906_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112115906:splice
112115906:variant
goto
C3orf52intron_variantc.650-736G>A
TMPRSS7
Testis
6.706
-0.149
461175
a0001 a0002 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0008c0010 others(1): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(6): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(70): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(116): Hide
0.327
224
270
10
chr3_112115906_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112115906:splice
112115906:variant
goto
C3orf52intron_variantc.650-736G>A
C3orf52
Testis
8.080
-0.179
461175
a0001 a0002 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0008c0010 others(1): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(6): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(70): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(116): Hide
0.327
224
270
10
chr3_112115906_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112115906:splice
112115906:variant
goto
C3orf52intron_variantc.650-736G>A
GCSAM
Testis
6.886
-0.281
461175
a0001 a0002 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0008c0010 others(1): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(6): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(70): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(116): Hide
0.327
224
270
10
chr3_112115906_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112115906:splice
112115906:variant
goto
C3orf52intron_variantc.650-736G>A
SLC9C1
Testis
47.833
0.473
461175
a0001 a0002 a0008 a0009
a0001c0001 a0001c0011 a0001c0012 a0002c0002 a0008c0010 others(1): Hide
a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(6): Hide
a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0017 others(70): Hide
HG00099.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00597.hp1 others(116): Hide
0.327
224
270
10
chr3_112115906_G_A_b38
+
MODIFIER
chr3
G
A
TogoVar
112114566:splice
112114566:variant
goto
C3orf52intron_variantc.649+1421T>C
CD200
Nerve_Tibial
4.418
0.107
44515
a0001 a0002 a0008 a0009
a0001c0001 a0002c0002 a0008c0010 a0009c0008
a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 a0008c0010t0002 a0009c0008t0002
a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(10): Hide
HG00099.hp1 HG00280.hp2 HG01069.hp2 HG01071.hp1 HG01074.hp1 others(22): Hide
0.229
268
306
10
chr3_112114566_T_C_b38
+
MODIFIER
chr3
T
C
TogoVar