rs113488022
|
|
490
|
0.351 |
0.840 |
7 |
140753336 |
missense variant
|
A/C;G;T
|
snv |
4.0E-06
|
|
0.020 |
1.000 |
2 |
2015 |
2016 |
rs121913377
|
|
480
|
0.354 |
0.840 |
7 |
140753335 |
missense variant
|
CA/AT;TT
|
mnv |
|
|
0.020 |
1.000 |
2 |
2015 |
2016 |
rs397507444
|
|
306
|
0.405 |
0.880 |
1 |
11794407 |
missense variant
|
T/G
|
snv |
|
|
0.020 |
1.000 |
2 |
2009 |
2013 |
rs1056503
|
|
4
|
0.851 |
0.200 |
5 |
83353158 |
synonymous variant
|
T/A;G
|
snv |
4.0E-06;
0.23
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs112445441
|
|
32
|
0.658 |
0.400 |
12 |
25245347 |
missense variant
|
C/A;G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs1159838942
|
|
1
|
1.000 |
0.120 |
11 |
36574757 |
missense variant
|
C/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs12355840
|
|
5
|
0.827 |
0.240 |
10 |
133247608 |
non coding transcript exon variant
|
C/G;T
|
snv |
1.1E-04;
0.80
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1308699981
|
|
7
|
0.807 |
0.440 |
1 |
161543085 |
missense variant
|
G/A
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs2228479
|
|
11
|
0.763 |
0.280 |
16 |
89919532 |
missense variant
|
G/A;C
|
snv |
7.8E-02;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs2682818
|
|
14
|
0.742 |
0.320 |
12 |
80935757 |
non coding transcript exon variant
|
A/C;T
|
snv |
0.83
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs28530648
|
|
1
|
1.000 |
0.120 |
6 |
32559302 |
intron variant
|
A/C;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs3020314
|
|
7
|
0.790 |
0.280 |
6 |
151949537 |
intron variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs3212961
|
|
7
|
0.827 |
0.200 |
19 |
45419065 |
intron variant
|
G/A;T
|
snv |
1.9E-04;
0.20
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs587781386
|
|
3
|
0.882 |
0.120 |
17 |
7674889 |
missense variant
|
A/C;G
|
snv |
3.2E-05;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs6054706
|
|
1
|
1.000 |
0.120 |
20 |
149223 |
downstream gene variant
|
C/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs6444305
|
|
2
|
0.925 |
0.120 |
3 |
188582114 |
intron variant
|
G/A;C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs7755224
|
|
1
|
1.000 |
0.120 |
6 |
32684540 |
regulatory region variant
|
A/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs854560
|
|
113
|
0.513 |
0.800 |
7 |
95316772 |
missense variant
|
A/C;G;N;T
|
snv |
0.29
|
|
0.010 |
1.000 |
1 |
2006 |
2006 |
rs9274614
|
|
1
|
1.000 |
0.120 |
6 |
32668069 |
intron variant
|
C/A;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs9275245
|
|
2
|
0.925 |
0.160 |
6 |
32693166 |
intergenic variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs9275572
|
|
15
|
0.724 |
0.360 |
6 |
32711222 |
upstream gene variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs587776632
|
|
2
|
0.925 |
0.120 |
1 |
85267901 |
frameshift variant
|
A/-;AAA
|
delins |
|
|
0.700 |
|
0 |
|
|
rs587776633
|
|
1
|
1.000 |
0.120 |
1 |
85270732 |
frameshift variant
|
-/T
|
delins |
|
|
0.700 |
|
0 |
|
|
rs587776634
|
|
1
|
1.000 |
0.120 |
1 |
85267788 |
frameshift variant
|
TGCCTACTTCTAGAACA/-
|
del |
|
|
0.700 |
|
0 |
|
|
rs587776635
|
|
1
|
1.000 |
0.120 |
1 |
85267919 |
frameshift variant
|
T/-
|
delins |
|
|
0.700 |
|
0 |
|
|