rs878853856
|
1.000 |
0.160 |
9 |
95453533 |
missense variant |
A/G
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.800 |
1.000 |
8 |
1996 |
2015 |
rs587776689
|
0.882 |
0.160 |
9 |
95453587 |
missense variant |
T/A;G
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
5 |
1996 |
2004 |
rs1060502268
|
1.000 |
0.160 |
9 |
95476835 |
missense variant |
C/T
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
4 |
2003 |
2013 |
rs1064793921
|
1.000 |
0.160 |
9 |
95476161 |
splice acceptor variant |
T/C;G
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
3 |
2006 |
2014 |
rs1131690986
|
1.000 |
0.160 |
9 |
95485866 |
stop gained |
G/A
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
3 |
1997 |
2006 |
rs863224443
|
1.000 |
0.160 |
9 |
95449942 |
splice acceptor variant |
T/C
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
3 |
2005 |
2006 |
rs1060502277
|
1.000 |
0.160 |
9 |
95476758 |
splice donor variant |
C/A;T
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
2 |
2006 |
2006 |
rs1554695039
|
1.000 |
0.160 |
9 |
95468939 |
stop gained |
G/A
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
2 |
1997 |
2012 |
rs878853849
|
1.000 |
0.160 |
9 |
95506601 |
splice acceptor variant |
T/C;G
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
2 |
2006 |
2006 |
rs878853852
|
1.000 |
0.160 |
9 |
95462000 |
splice acceptor variant |
T/A;C
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
2 |
2006 |
2006 |
rs1131690985
|
0.925 |
0.200 |
9 |
95449891 |
missense variant |
C/T
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.010 |
1.000 |
1 |
2000 |
2000 |
rs1249050389
|
0.925 |
0.240 |
9 |
95485696 |
stop gained |
G/C
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs1564055606
|
1.000 |
0.160 |
9 |
95480462 |
stop gained |
G/C
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs199476090
|
1.000 |
0.160 |
9 |
95479134 |
stop gained |
G/A
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
1.000 |
1 |
1996 |
1996 |
rs755103500
|
0.851 |
0.160 |
9 |
95516820 |
start lost |
T/C;G
|
snv
|
8.4E-06;
4.2E-06
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs766905791
|
0.851 |
0.160 |
9 |
95485815 |
start lost |
T/C
|
snv
|
1.2E-05
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs773304123
|
1.000 |
0.160 |
9 |
95467363 |
synonymous variant |
C/T
|
snv
|
1.2E-05
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs1057520590
|
1.000 |
0.160 |
9 |
95482204 |
splice acceptor variant |
C/G
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1060502271
|
1.000 |
0.160 |
9 |
95479149 |
splice acceptor variant |
T/A
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1060502274
|
1.000 |
0.160 |
9 |
95469119 |
stop gained |
G/A
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1060502278
|
1.000 |
0.160 |
9 |
95458207 |
stop gained |
C/A
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1060502281
|
1.000 |
0.160 |
9 |
95481954 |
stop gained |
G/T
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1060502285
|
1.000 |
0.160 |
9 |
95456414 |
splice acceptor variant |
C/T
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1060502287
|
1.000 |
0.160 |
9 |
95481987 |
stop gained |
C/T
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1060502298
|
1.000 |
0.160 |
9 |
95458178 |
stop gained |
A/T
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|