rs1060499958
|
1.000 |
0.160 |
19 |
1219356 |
missense variant |
T/C
|
snv
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1060499960
|
1.000 |
0.160 |
19 |
1223051 |
frameshift variant |
ACCGGTGG/-
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1060499961
|
1.000 |
0.160 |
19 |
1207041 |
frameshift variant |
C/-
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1131690920
|
1.000 |
0.160 |
19 |
1222007 |
splice donor variant |
G/A
|
snv
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1131690949
|
1.000 |
0.160 |
19 |
1221320 |
frameshift variant |
-/G
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1131690950
|
1.000 |
0.160 |
19 |
1207204 |
splice donor variant |
G/A;C
|
snv
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs121913324
|
1.000 |
0.160 |
19 |
1207022 |
stop gained |
C/T
|
snv
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs137853075
|
1.000 |
0.160 |
19 |
1221237 |
stop gained |
C/A;T
|
snv
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs137854584
|
1.000 |
0.160 |
19 |
1207082 |
stop gained |
G/T
|
snv
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555735001
|
1.000 |
0.160 |
19 |
1207091 |
frameshift variant |
-/AC
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555735008
|
1.000 |
0.160 |
19 |
1207093 |
frameshift variant |
C/-
|
del
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555735014
|
1.000 |
0.160 |
19 |
1207112 |
frameshift variant |
C/-
|
del
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555737480
|
1.000 |
0.160 |
19 |
1218502 |
splice donor variant |
T/C
|
snv
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555738219
|
1.000 |
0.160 |
19 |
1220431 |
frameshift variant |
-/GGACATCA
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555738475
|
0.776 |
0.400 |
19 |
1220707 |
frameshift variant |
G/-
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555738656
|
1.000 |
0.160 |
19 |
1221270 |
frameshift variant |
-/GA
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555738667
|
1.000 |
0.160 |
19 |
1221294 |
frameshift variant |
C/-
|
del
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555738723
|
1.000 |
0.160 |
19 |
1221329 |
frameshift variant |
A/-
|
del
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555738863
|
1.000 |
0.160 |
19 |
1221969 |
frameshift variant |
CCAAG/-
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555738874
|
1.000 |
0.160 |
19 |
1221979 |
frameshift variant |
-/TCCATCC
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1555738899
|
1.000 |
0.160 |
19 |
1222004 |
frameshift variant |
CA/TCC
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1568689930
|
1.000 |
0.160 |
19 |
1206993 |
frameshift variant |
-/C
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1568689994
|
1.000 |
0.160 |
19 |
1207017 |
frameshift variant |
CT/-
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1568690161
|
1.000 |
0.160 |
19 |
1207064 |
frameshift variant |
-/T
|
delins
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs397518440
|
1.000 |
0.160 |
19 |
1219367 |
frameshift variant |
C/-
|
del
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|