138120673:splice
138120673:variant
goto
A4GNTdownstream_gene_variantc.*3591T>C others(3): Hide
A4GNT
Adipose_Subcutaneous
3.646
0.837
71123198
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0002c0002 others(6): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(18): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(193): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp1 others(386): Hide
0.990
13
14
10
chr3_138120673_A_G_b38
-
MODIFIER
chr3
A
G
TogoVar
138120673:splice
138120673:variant
goto
A4GNTdownstream_gene_variantc.*3591T>C others(3): Hide
A4GNT
Adipose_Visceral_Omentum
4.231
0.865
71123198
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0002c0002 others(6): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(18): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(193): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp1 others(386): Hide
0.986
14
16
10
chr3_138120673_A_G_b38
-
MODIFIER
chr3
A
G
TogoVar
138120673:splice
138120673:variant
goto
A4GNTdownstream_gene_variantc.*3591T>C others(3): Hide
A4GNT
Artery_Tibial
6.076
1.050
71123198
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0002c0002 others(6): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(18): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(193): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp1 others(386): Hide
0.987
16
18
10
chr3_138120673_A_G_b38
-
MODIFIER
chr3
A
G
TogoVar
138120673:splice
138120673:variant
goto
A4GNTdownstream_gene_variantc.*3591T>C others(3): Hide
A4GNT
Cells_Cultured_fibroblasts
6.152
1.009
71123198
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0002c0002 others(6): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(18): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(193): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp1 others(386): Hide
0.988
13
15
10
chr3_138120673_A_G_b38
-
MODIFIER
chr3
A
G
TogoVar
138120673:splice
138120673:variant
goto
A4GNTdownstream_gene_variantc.*3591T>C others(3): Hide
A4GNT
Colon_Transverse
4.024
0.947
71123198
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0002c0002 others(6): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(18): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(193): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp1 others(386): Hide
0.985
13
14
10
chr3_138120673_A_G_b38
-
MODIFIER
chr3
A
G
TogoVar
138120673:splice
138120673:variant
goto
A4GNTdownstream_gene_variantc.*3591T>C others(3): Hide
A4GNT
Esophagus_Muscularis
4.682
1.264
71123198
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0002c0002 others(6): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(18): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(193): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp1 others(386): Hide
0.991
10
10
10
chr3_138120673_A_G_b38
-
MODIFIER
chr3
A
G
TogoVar
138120673:splice
138120673:variant
goto
A4GNTdownstream_gene_variantc.*3591T>C others(3): Hide
A4GNT
Nerve_Tibial
5.468
0.951
71123198
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0002c0002 others(6): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(18): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(193): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp1 others(386): Hide
0.986
17
19
10
chr3_138120673_A_G_b38
-
MODIFIER
chr3
A
G
TogoVar
138120673:splice
138120673:variant
goto
A4GNTdownstream_gene_variantc.*3591T>C others(3): Hide
ESYT3
Nerve_Tibial
3.751
-0.351
71123198
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0002c0002 others(6): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(18): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(193): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp1 others(386): Hide
0.986
17
19
10
chr3_138120673_A_G_b38
-
MODIFIER
chr3
A
G
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Adipose_Subcutaneous
63.304
0.712
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
394
485
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Adipose_Subcutaneous
63.304
0.712
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
394
485
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Adipose_Subcutaneous
63.304
0.712
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
394
485
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Adipose_Visceral_Omentum
47.413
0.714
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.665
316
391
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Adipose_Visceral_Omentum
47.413
0.714
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.665
316
391
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Adipose_Visceral_Omentum
47.413
0.714
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.665
316
391
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Adrenal_Gland
10.251
0.460
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
161
201
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Adrenal_Gland
10.251
0.460
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
161
201
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Adrenal_Gland
10.251
0.460
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
161
201
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Artery_Aorta
31.639
0.701
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
263
327
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Artery_Aorta
31.639
0.701
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
263
327
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Artery_Aorta
31.639
0.701
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
263
327
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
MRAS
Artery_Aorta
11.859
-0.319
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
263
327
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
MRAS
Artery_Aorta
11.859
-0.319
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
263
327
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
MRAS
Artery_Aorta
11.859
-0.319
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
263
327
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
ESYT3
Artery_Aorta
5.343
-0.192
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
263
327
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
ESYT3
Artery_Aorta
5.343
-0.192
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
263
327
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
ESYT3
Artery_Aorta
5.343
-0.192
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
263
327
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Artery_Coronary
15.446
0.661
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.687
137
168
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Artery_Coronary
15.446
0.661
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.687
137
168
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Artery_Coronary
15.446
0.661
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.687
137
168
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Artery_Tibial
39.695
0.642
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.663
382
464
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Artery_Tibial
39.695
0.642
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.663
382
464
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Artery_Tibial
39.695
0.642
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.663
382
464
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
MRAS
Artery_Tibial
4.420
-0.106
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.663
382
464
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
MRAS
Artery_Tibial
4.420
-0.106
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.663
382
464
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
MRAS
Artery_Tibial
4.420
-0.106
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.663
382
464
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Bladder
6.743
0.789
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.682
39
49
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Bladder
6.743
0.789
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.682
39
49
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Bladder
6.743
0.789
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.682
39
49
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Brain_Amygdala
5.315
0.379
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.644
104
128
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Brain_Amygdala
5.315
0.379
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.644
104
128
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Brain_Amygdala
5.315
0.379
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.644
104
128
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Brain_Caudate_basal_ganglia
12.402
0.432
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
164
206
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Brain_Caudate_basal_ganglia
12.402
0.432
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
164
206
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Brain_Caudate_basal_ganglia
12.402
0.432
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.654
164
206
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Brain_Cerebellar_Hemisphere
5.337
0.370
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.639
159
199
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Brain_Cerebellar_Hemisphere
5.337
0.370
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.639
159
199
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Brain_Cerebellar_Hemisphere
5.337
0.370
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.639
159
199
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Brain_Cerebellum
6.816
0.444
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.646
154
187
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Brain_Cerebellum
6.816
0.444
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.646
154
187
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Brain_Cerebellum
6.816
0.444
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.646
154
187
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Brain_Cortex
9.259
0.522
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.660
146
182
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Brain_Cortex
9.259
0.522
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.660
146
182
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Brain_Cortex
9.259
0.522
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.660
146
182
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Brain_Frontal_Cortex_BA9
8.825
0.477
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.662
144
181
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Brain_Frontal_Cortex_BA9
8.825
0.477
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.662
144
181
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Brain_Frontal_Cortex_BA9
8.825
0.477
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.662
144
181
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
NME9
Brain_Frontal_Cortex_BA9
4.146
0.253
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.662
144
181
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
NME9
Brain_Frontal_Cortex_BA9
4.146
0.253
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.662
144
181
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
NME9
Brain_Frontal_Cortex_BA9
4.146
0.253
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.662
144
181
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Brain_Hypothalamus
6.558
0.376
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.646
146
181
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Brain_Hypothalamus
6.558
0.376
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.646
146
181
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Brain_Hypothalamus
6.558
0.376
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.646
146
181
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Brain_Nucleus_accumbens_basal_ganglia
7.830
0.422
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.658
157
194
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Brain_Nucleus_accumbens_basal_ganglia
7.830
0.422
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.658
157
194
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Brain_Nucleus_accumbens_basal_ganglia
7.830
0.422
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.658
157
194
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
NME9
Brain_Nucleus_accumbens_basal_ganglia
4.142
0.194
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.658
157
194
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
NME9
Brain_Nucleus_accumbens_basal_ganglia
4.142
0.194
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.658
157
194
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
NME9
Brain_Nucleus_accumbens_basal_ganglia
4.142
0.194
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.658
157
194
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Brain_Spinal_cord_cervical_c-1
4.384
0.314
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.663
105
137
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Brain_Spinal_cord_cervical_c-1
4.384
0.314
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.663
105
137
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Brain_Spinal_cord_cervical_c-1
4.384
0.314
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.663
105
137
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Brain_Substantia_nigra
5.398
0.435
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.678
93
118
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Brain_Substantia_nigra
5.398
0.435
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.678
93
118
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Brain_Substantia_nigra
5.398
0.435
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.678
93
118
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Breast_Mammary_Tissue
32.640
0.647
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.651
290
357
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Breast_Mammary_Tissue
32.640
0.647
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.651
290
357
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Breast_Mammary_Tissue
32.640
0.647
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.651
290
357
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Cells_Cultured_fibroblasts
80.735
0.784
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.669
349
430
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Cells_Cultured_fibroblasts
80.735
0.784
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.669
349
430
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Cells_Cultured_fibroblasts
80.735
0.784
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.669
349
430
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
DZIP1L
Colon_Sigmoid
5.937
0.170
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.664
229
281
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
DZIP1L
Colon_Sigmoid
5.937
0.170
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.664
229
281
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
DZIP1L
Colon_Sigmoid
5.937
0.170
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.664
229
281
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Colon_Sigmoid
24.174
0.639
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.664
229
281
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Colon_Sigmoid
24.174
0.639
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.664
229
281
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Colon_Sigmoid
24.174
0.639
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.664
229
281
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Colon_Transverse
19.448
0.520
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
263
326
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Colon_Transverse
19.448
0.520
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
263
326
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Colon_Transverse
19.448
0.520
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
263
326
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Esophagus_Gastroesophageal_Junction
28.037
0.745
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
224
275
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Esophagus_Gastroesophageal_Junction
28.037
0.745
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
224
275
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Esophagus_Gastroesophageal_Junction
28.037
0.745
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.659
224
275
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Esophagus_Mucosa
25.334
0.534
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.658
337
420
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Esophagus_Mucosa
25.334
0.534
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.658
337
420
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Esophagus_Mucosa
25.334
0.534
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.658
337
420
10
chr3_138124634_G_T_b38
-
MODERATE
chr3
G
T
TogoVar
138123250:splice
138123250:variant
goto
A4GNTdownstream_gene_variantc.*1014C>T others(3): Hide
A4GNT
Esophagus_Muscularis
25.135
0.579
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.666
315
375
10
chr3_138123250_G_A_b38
-
MODIFIER
chr3
G
A
TogoVar
138124264:splice
138124264:variant
goto
A4GNTstop_retained_variantc.1023A>G others(11): Hide
A4GNT
Esophagus_Muscularis
25.135
0.579
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide
HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00323.hp2 HG00408.hp2 others(238): Hide
0.666
315
375
10
chr3_138124264_T_C_b38
-
LOW
chr3
T
C
TogoVar
138124634:splice
138124634:variant
goto
A4GNTmissense_variantc.653C>Ap.Ala2 others(5): Hide
A4GNT
Esophagus_Muscularis
25.135
0.579
4714163
a0001 a0004 a0005 a0007
a0001c0001 a0001c0003 a0001c0009 a0001c0012 a0004c0007 others(2): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 a0001c0003t0001 others(9): Hide
a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Hide