rs79658334
|
0.662 |
0.360 |
10 |
43119548 |
missense variant |
G/A;C;T
|
snv
|
1.2E-04;
4.3E-06
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.880 |
1.000 |
16 |
1996 |
2018 |
rs76262710
|
0.724 |
0.280 |
10 |
43113648 |
missense variant |
T/A;C;G
|
snv
|
4.0E-06;
4.0E-06
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.870 |
1.000 |
34 |
1993 |
2018 |
rs75234356
|
0.716 |
0.240 |
10 |
43120144 |
missense variant |
T/G
|
snv
|
1.2E-05
|
7.0E-06
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.870 |
1.000 |
27 |
1993 |
2018 |
rs79781594
|
0.732 |
0.160 |
10 |
43113649 |
missense variant |
G/A;C;T
|
snv
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.830 |
1.000 |
31 |
1993 |
2018 |
rs78014899
|
0.742 |
0.160 |
10 |
43118392 |
missense variant |
G/A;C;T
|
snv
|
8.0E-06
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.830 |
1.000 |
11 |
1996 |
2018 |
rs75030001
|
0.807 |
0.160 |
10 |
43118458 |
missense variant |
G/C;T
|
snv
|
4.0E-06;
2.0E-05
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.830 |
1.000 |
3 |
2012 |
2018 |
rs75996173
|
0.716 |
0.240 |
10 |
43114501 |
missense variant |
G/A;C;T
|
snv
|
4.0E-06;
4.0E-06
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.820 |
1.000 |
30 |
1993 |
2018 |
rs77724903
|
0.672 |
0.280 |
10 |
43118460 |
missense variant |
A/G;T
|
snv
|
4.0E-06;
2.1E-03
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.810 |
1.000 |
21 |
1993 |
2007 |
rs77503355
|
0.776 |
0.160 |
10 |
43113655 |
missense variant |
G/A;C;T
|
snv
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.800 |
1.000 |
8 |
1996 |
2017 |
rs77939446
|
0.724 |
0.120 |
10 |
43113622 |
missense variant |
G/A;C;T
|
snv
|
4.0E-06
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.800 |
1.000 |
8 |
1996 |
2017 |
rs74799832
|
0.662 |
0.280 |
10 |
43121968 |
missense variant |
T/C
|
snv
|
4.0E-06
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.770 |
1.000 |
7 |
1996 |
2018 |
rs75076352
|
0.689 |
0.240 |
10 |
43114500 |
missense variant |
T/A;C;G
|
snv
|
1.2E-05
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.740 |
1.000 |
4 |
1994 |
2018 |
rs75873440
|
0.763 |
0.200 |
10 |
43112173 |
missense variant |
G/A;T
|
snv
|
4.4E-05
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.730 |
1.000 |
3 |
2003 |
2008 |
rs77316810
|
0.776 |
0.200 |
10 |
43113654 |
missense variant |
T/A;C;G
|
snv
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.730 |
1.000 |
3 |
1994 |
2018 |
rs77709286
|
0.752 |
0.160 |
10 |
43114502 |
missense variant |
C/G
|
snv
|
4.0E-06
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.710 |
1.000 |
21 |
1993 |
2004 |
rs55947360
|
1.000 |
0.120 |
10 |
43119669 |
missense variant |
G/A;T
|
snv
|
4.0E-05;
4.0E-06
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.700 |
1.000 |
20 |
1993 |
2001 |
rs80069458
|
0.882 |
0.120 |
10 |
43113629 |
missense variant |
C/G;T
|
snv
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.700 |
1.000 |
20 |
1993 |
2001 |
rs377767434
|
1.000 |
0.120 |
10 |
43112153 |
protein altering variant |
-/AGGAGTGTG
|
delins
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.700 |
1.000 |
1 |
1999 |
1999 |
rs377767391
|
0.827 |
0.160 |
10 |
43113627 |
missense variant |
T/A;C;G
|
snv
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.700 |
|
0 |
|
|
rs377767405
|
0.827 |
0.120 |
10 |
43114489 |
missense variant |
G/A;C;T
|
snv
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.700 |
|
0 |
|
|
rs377767412
|
0.790 |
0.240 |
10 |
43114547 |
synonymous variant |
G/A
|
snv
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.700 |
|
0 |
|
|
rs377767432
|
0.925 |
0.160 |
10 |
43121980 |
missense variant |
C/A;T
|
snv
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.700 |
|
0 |
|
|
rs77558292
|
0.776 |
0.160 |
10 |
43113621 |
missense variant |
T/A;C;G
|
snv
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.700 |
|
0 |
|
|
rs78347871
|
0.882 |
0.120 |
10 |
43121950 |
missense variant |
G/A;C;T
|
snv
|
8.0E-06;
2.0E-05
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.700 |
|
0 |
|
|
rs377767397
|
0.790 |
0.280 |
10 |
43113628 |
missense variant |
G/A;C;T
|
snv
|
|
|
Familial medullary thyroid carcinoma
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
|
0.030 |
1.000 |
3 |
2001 |
2018 |