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 |
|
|
rs1060502264
|
1.000 |
0.160 |
9 |
95449930 |
frameshift variant |
C/-
|
del
|
|
|
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 |
|
|
rs1060502273
|
1.000 |
0.160 |
9 |
95453562 |
frameshift variant |
AT/-
|
del
|
|
|
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 |
|
|
rs1060502280
|
1.000 |
0.160 |
9 |
95485814 |
frameshift variant |
TA/-
|
delins
|
|
|
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 |
|
|
rs1060502286
|
1.000 |
0.160 |
9 |
95479006 |
frameshift variant |
AT/-
|
delins
|
|
|
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 |
|
|
rs1060502294
|
1.000 |
0.160 |
9 |
95467333 |
frameshift variant |
-/A
|
delins
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1060502295
|
1.000 |
0.160 |
9 |
95478094 |
frameshift variant |
G/-
|
del
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1060502297
|
1.000 |
0.160 |
9 |
95479060 |
frameshift variant |
G/-
|
del
|
|
|
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 |
|
|
rs1060502301
|
1.000 |
0.160 |
9 |
95458029 |
stop gained |
C/T
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1064793922
|
1.000 |
0.160 |
9 |
95482198 |
stop gained |
C/A;T
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1131690969
|
1.000 |
0.160 |
9 |
95480525 |
frameshift variant |
CTTT/-
|
delins
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1333346461
|
1.000 |
0.160 |
9 |
95485690 |
stop gained |
G/A;T
|
snv
|
|
7.0E-06
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1344258746
|
1.000 |
0.160 |
9 |
95485821 |
stop gained |
C/A;T
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1356231878
|
1.000 |
0.160 |
9 |
95459685 |
stop gained |
A/C;G
|
snv
|
4.0E-06
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1432645175
|
1.000 |
0.160 |
9 |
95479006 |
stop gained |
A/C;G
|
snv
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1554689667
|
1.000 |
0.160 |
9 |
95449847 |
frameshift variant |
ATAT/GGA
|
delins
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1554690411
|
1.000 |
0.160 |
9 |
95453498 |
frameshift variant |
GA/-
|
delins
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|
rs1554691354
|
1.000 |
0.160 |
9 |
95458055 |
frameshift variant |
-/A
|
delins
|
|
|
Basal Cell Nevus Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
|
0.700 |
|
0 |
|
|