rs74315403
|
|
10
|
0.790 |
0.200 |
20 |
4699752 |
missense variant
|
G/A
|
snv |
|
|
0.800 |
0.955 |
22 |
1990 |
2015 |
rs398122370
|
|
4
|
0.925 |
0.160 |
20 |
4699851 |
missense variant
|
G/C
|
snv |
|
|
0.830 |
1.000 |
13 |
1990 |
2010 |
rs74315401
|
|
32
|
0.683 |
0.320 |
20 |
4699525 |
missense variant
|
C/T
|
snv |
|
|
0.040 |
1.000 |
4 |
1995 |
2013 |
rs11538758
|
|
8
|
0.882 |
0.160 |
20 |
4699534 |
missense variant
|
C/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1178466848
|
|
4
|
0.925 |
0.120 |
20 |
4699785 |
missense variant
|
G/A
|
snv |
|
2.8E-05
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1191139947
|
|
3
|
0.882 |
0.120 |
20 |
4699935 |
missense variant
|
C/T
|
snv |
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs1405757246
|
|
3
|
0.882 |
0.120 |
19 |
34379521 |
missense variant
|
T/C
|
snv |
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs1460163
|
|
1
|
1.000 |
0.120 |
8 |
79315213 |
downstream gene variant
|
G/A;T
|
snv |
|
|
0.800 |
1.000 |
1 |
2009 |
2009 |
rs1473972013
|
|
3
|
0.925 |
0.160 |
1 |
47035911 |
missense variant
|
G/A
|
snv |
|
7.0E-06
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs16840647
|
|
1
|
1.000 |
0.120 |
1 |
240799770 |
intron variant
|
A/G
|
snv |
|
4.1E-02
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs2065706
|
|
1
|
1.000 |
0.120 |
20 |
4702649 |
downstream gene variant
|
T/C
|
snv |
|
0.17
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs295301
|
|
5
|
0.851 |
0.160 |
3 |
141619799 |
downstream gene variant
|
G/A
|
snv |
|
0.38
|
0.010 |
< 0.001 |
1 |
2012 |
2012 |
rs3863150
|
|
1
|
1.000 |
0.120 |
5 |
41506758 |
intron variant
|
T/C
|
snv |
|
0.11
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs4921542
|
|
1
|
1.000 |
0.120 |
8 |
17348068 |
intron variant
|
T/G
|
snv |
|
0.19
|
0.800 |
1.000 |
1 |
2012 |
2012 |
rs6052780
|
|
1
|
1.000 |
0.120 |
20 |
4708828 |
intergenic variant
|
G/A;T
|
snv |
|
7.1E-02
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs6107516
|
|
2
|
1.000 |
0.120 |
20 |
4696446 |
intron variant
|
G/A
|
snv |
|
0.23
|
0.800 |
1.000 |
1 |
2012 |
2012 |
rs6116492
|
|
1
|
1.000 |
0.120 |
20 |
4717980 |
upstream gene variant
|
G/T
|
snv |
|
7.0E-02
|
0.800 |
1.000 |
1 |
2012 |
2012 |
rs63751249
|
|
1
|
1.000 |
0.120 |
17 |
45996620 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs676328
|
|
1
|
1.000 |
0.120 |
5 |
41505587 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs74315402
|
|
7
|
0.882 |
0.200 |
20 |
4699570 |
missense variant
|
C/T
|
snv |
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs74315405
|
|
6
|
0.827 |
0.160 |
20 |
4699813 |
missense variant
|
T/C
|
snv |
|
|
0.010 |
1.000 |
1 |
1998 |
1998 |
rs74315413
|
|
8
|
0.807 |
0.160 |
20 |
4699780 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2004 |
2004 |
rs7565981
|
|
1
|
1.000 |
0.120 |
2 |
100807869 |
intergenic variant
|
G/A
|
snv |
|
0.15
|
0.800 |
1.000 |
1 |
2012 |
2012 |
rs8074026
|
|
3
|
0.882 |
0.160 |
17 |
1753779 |
intron variant
|
T/C
|
snv |
|
0.71
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs193922906
|
|
4
|
0.882 |
0.160 |
20 |
4699380 |
inframe insertion
|
TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC/-;TCATGGTGGTGGCTGGGGGCAGCC;TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC;TCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCC
|
delins |
|
|
0.700 |
|
0 |
|
|