rs74315401
|
|
32
|
0.683 |
0.320 |
20 |
4699525 |
missense variant
|
C/T
|
snv |
|
|
0.900 |
0.979 |
47 |
1989 |
2019 |
rs74315405
|
|
6
|
0.827 |
0.160 |
20 |
4699813 |
missense variant
|
T/C
|
snv |
|
|
0.880 |
1.000 |
19 |
1989 |
2019 |
rs74315413
|
|
8
|
0.807 |
0.160 |
20 |
4699780 |
missense variant
|
A/G
|
snv |
|
|
0.820 |
1.000 |
13 |
1989 |
2018 |
rs74315406
|
|
5
|
0.851 |
0.160 |
20 |
4699870 |
missense variant
|
A/G
|
snv |
|
|
0.810 |
1.000 |
12 |
1989 |
2010 |
rs74315402
|
|
7
|
0.882 |
0.200 |
20 |
4699570 |
missense variant
|
C/T
|
snv |
|
|
0.780 |
1.000 |
8 |
1997 |
2019 |
rs11538758
|
|
8
|
0.882 |
0.160 |
20 |
4699534 |
missense variant
|
C/A;T
|
snv |
|
|
0.760 |
1.000 |
6 |
1999 |
2018 |
rs1055679036
|
|
1
|
1.000 |
0.120 |
19 |
12800207 |
missense variant
|
A/G
|
snv |
|
|
0.020 |
1.000 |
2 |
2018 |
2019 |
rs111512673
|
|
1
|
1.000 |
0.120 |
4 |
184632303 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs12882491
|
|
3
|
0.925 |
0.160 |
14 |
102816936 |
intron variant
|
C/T
|
snv |
|
0.51
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs17852079
|
|
1
|
1.000 |
0.120 |
20 |
4699899 |
stop gained
|
C/A;T
|
snv |
|
|
0.710 |
1.000 |
1 |
2010 |
2010 |
rs2081687
|
|
6
|
0.882 |
0.240 |
8 |
58476006 |
intergenic variant
|
T/C
|
snv |
|
0.70
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs3808607
|
|
16
|
0.716 |
0.400 |
8 |
58500365 |
upstream gene variant
|
G/T
|
snv |
|
0.55
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs398122370
|
|
4
|
0.925 |
0.160 |
20 |
4699851 |
missense variant
|
G/C
|
snv |
|
|
0.010 |
1.000 |
1 |
2000 |
2000 |
rs398122414
|
|
3
|
0.925 |
0.120 |
20 |
4699898 |
stop gained
|
C/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs74315403
|
|
10
|
0.790 |
0.200 |
20 |
4699752 |
missense variant
|
G/A
|
snv |
|
|
0.010 |
1.000 |
1 |
1998 |
1998 |
rs7932167
|
|
2
|
0.925 |
0.160 |
11 |
620599 |
intron variant
|
G/T
|
snv |
|
0.73
|
0.010 |
< 0.001 |
1 |
2011 |
2011 |
rs80356489
|
|
3
|
0.882 |
0.200 |
11 |
119028223 |
missense variant
|
A/G
|
snv |
|
7.0E-06
|
0.010 |
1.000 |
1 |
1998 |
1998 |
rs193922906
|
|
4
|
0.882 |
0.160 |
20 |
4699380 |
inframe insertion
|
TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC/-;TCATGGTGGTGGCTGGGGGCAGCC;TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC;TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC
|
delins |
|
|
0.700 |
|
0 |
|
|
rs398122413
|
|
1
|
1.000 |
0.120 |
20 |
4699853 |
missense variant
|
G/C
|
snv |
|
|
0.700 |
|
0 |
|
|
rs74315415
|
|
1
|
1.000 |
0.120 |
20 |
4699618 |
missense variant
|
C/T
|
snv |
|
|
0.700 |
|
0 |
|
|
rs761807915
|
|
4
|
0.925 |
0.120 |
20 |
4699824 |
missense variant
|
G/A
|
snv |
4.0E-06
|
7.0E-06
|
0.720 |
1.000 |
13 |
1989 |
2013 |
rs28933385
|
|
25
|
0.695 |
0.320 |
20 |
4699818 |
missense variant
|
G/A
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
1999 |
1999 |
rs74315410
|
|
2
|
1.000 |
0.120 |
20 |
4699612 |
missense variant
|
G/T
|
snv |
4.0E-06
|
|
0.830 |
1.000 |
13 |
1989 |
2019 |
rs753438778
|
|
2
|
0.925 |
0.160 |
5 |
132074925 |
missense variant
|
C/G;T
|
snv |
8.0E-06;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs74315414
|
|
5
|
0.882 |
0.200 |
20 |
4699533 |
missense variant
|
C/A;T
|
snv |
4.0E-06
|
|
0.700 |
|
0 |
|
|