rs28904921
|
0.763 |
0.320 |
11 |
108329202 |
missense variant |
T/G
|
snv
|
4.0E-05
|
6.3E-05
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
21 |
1996 |
2016 |
rs587779852
|
0.882 |
0.280 |
11 |
108312424 |
stop gained |
G/T
|
snv
|
4.4E-05
|
3.5E-05
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
19 |
1998 |
2018 |
rs587776547
|
0.882 |
0.320 |
11 |
108331885 |
inframe deletion |
TAGAATTTC/-
|
delins
|
2.8E-05
|
1.4E-05
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
13 |
1996 |
2011 |
rs587779866
|
0.925 |
0.280 |
11 |
108331877 |
splice acceptor variant |
A/C;G
|
snv
|
8.0E-06
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
11 |
1998 |
2016 |
rs587782652
|
0.851 |
0.320 |
11 |
108335105 |
missense variant |
T/C
|
snv
|
3.2E-05
|
4.2E-05
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
11 |
2002 |
2016 |
rs564652222
|
0.925 |
0.280 |
11 |
108325416 |
missense variant |
C/A;T
|
snv
|
|
1.4E-05
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
10 |
1999 |
2013 |
rs587781894
|
0.882 |
0.360 |
11 |
108365360 |
missense variant |
G/A;C
|
snv
|
8.0E-06
|
7.0E-06
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
10 |
1999 |
2013 |
rs371638537
|
1.000 |
0.200 |
11 |
108335959 |
stop gained |
A/C;G;T
|
snv
|
1.6E-05
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
9 |
1996 |
2017 |
rs587781299
|
0.925 |
0.280 |
11 |
108327665 |
frameshift variant |
-/A
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
8 |
1998 |
2016 |
rs587781905
|
1.000 |
0.200 |
11 |
108331442 |
splice region variant |
GAGA/-
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
8 |
1996 |
2011 |
rs730881294
|
1.000 |
0.200 |
11 |
108335957 |
frameshift variant |
ATAAG/-
|
del
|
8.0E-06
|
2.8E-05
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
8 |
1998 |
2017 |
rs730881295
|
1.000 |
0.200 |
11 |
108343372 |
splice region variant |
GTGA/-
|
delins
|
|
2.1E-05
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
8 |
1996 |
2017 |
rs770641163
|
0.882 |
0.360 |
11 |
108365208 |
stop gained |
C/G;T
|
snv
|
4.0E-06;
1.2E-05
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
8 |
1996 |
2017 |
rs786202800
|
1.000 |
0.200 |
11 |
108343338 |
frameshift variant |
TTTCAGTGCC/-
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
8 |
1998 |
2017 |
rs139770721
|
0.925 |
0.280 |
11 |
108315911 |
missense variant |
G/A
|
snv
|
2.8E-05
|
7.0E-06
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
7 |
1999 |
2016 |
rs17174393
|
0.882 |
0.280 |
11 |
108353881 |
splice donor variant |
G/A;C;T
|
snv
|
1.6E-05
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
7 |
1996 |
2016 |
rs267606668
|
1.000 |
0.200 |
11 |
108332848 |
missense variant |
TG/GC
|
mnv
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
7 |
1998 |
2013 |
rs377349459
|
0.925 |
0.280 |
11 |
108332886 |
stop gained |
G/A
|
snv
|
4.0E-06
|
5.6E-05
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
7 |
1998 |
2017 |
rs587779872
|
1.000 |
0.200 |
11 |
108345818 |
missense variant |
C/T
|
snv
|
3.2E-05
|
1.4E-05
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
7 |
1998 |
2017 |
rs587782719
|
0.882 |
0.240 |
11 |
108335080 |
missense variant |
G/A;C;T
|
snv
|
4.0E-06
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
7 |
2006 |
2013 |
rs769142993
|
0.851 |
0.280 |
11 |
108331498 |
missense variant |
G/C;T
|
snv
|
2.4E-05
|
7.0E-06
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
7 |
2000 |
2012 |
rs774925473
|
0.925 |
0.200 |
11 |
108309110 |
intron variant |
A/G
|
snv
|
2.4E-05
|
4.2E-05
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
7 |
1996 |
2017 |
rs864622185
|
1.000 |
0.200 |
11 |
108332759 |
splice region variant |
T/G
|
snv
|
4.0E-06
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
7 |
1996 |
2015 |
rs121434220
|
1.000 |
0.200 |
11 |
108330233 |
stop gained |
C/T
|
snv
|
4.0E-06
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
6 |
1996 |
2016 |
rs397514577
|
0.882 |
0.280 |
11 |
108317374 |
missense variant |
C/A
|
snv
|
4.0E-06
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
6 |
1999 |
2015 |