rs1131690929
|
|
|
19 |
1207121 |
frameshift variant |
-/A
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
|
0 |
|
|
rs1131690952
|
|
|
19 |
1218495 |
frameshift variant |
-/A
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
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 |
|
|
rs1131690922
|
|
|
19 |
1220403 |
frameshift variant |
-/ACCT
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
|
0 |
|
|
rs786205864
|
1.000 |
0.160 |
19 |
1221321 |
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 |
1.000 |
3 |
2000 |
2005 |
rs1131690930
|
|
|
19 |
1207004 |
frameshift variant |
-/C
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
|
0 |
|
|
rs1131690946
|
|
|
19 |
1220588 |
frameshift variant |
-/C
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
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 |
|
|
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 |
|
|
rs1131690949
|
1.000 |
0.160 |
19 |
1221320 |
frameshift variant |
-/G
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
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 |
|
|
rs1131690933
|
|
|
19 |
1218488 |
frameshift variant |
-/GAAGC
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
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 |
|
|
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 |
|
|
rs397518441
|
1.000 |
0.160 |
19 |
1207109 |
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 |
|
|
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 |
|
|
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 |
|
|
rs587781856
|
|
|
19 |
1220479 |
frameshift variant |
A/-
|
delins
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
|
0 |
|
|
rs1131690931
|
|
|
19 |
1220371 |
splice acceptor variant |
A/C
|
snv
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
1 |
2001 |
2001 |
rs727504172
|
1.000 |
0.160 |
19 |
1222983 |
splice acceptor variant |
A/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 |
|
|
rs886037859
|
1.000 |
0.160 |
19 |
1220450 |
missense variant |
A/G
|
snv
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
5 |
1999 |
2013 |
rs1131690951
|
|
|
19 |
1218501 |
splice donor variant |
A/G
|
snv
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
4 |
2002 |
2007 |
rs876658584
|
1.000 |
0.160 |
19 |
1218415 |
splice acceptor variant |
A/G
|
snv
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
4 |
1999 |
2013 |
rs1131690934
|
|
|
19 |
1220579 |
splice acceptor variant |
A/G
|
snv
|
|
|
Neoplastic Syndromes, Hereditary
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
|
0.700 |
1.000 |
2 |
2001 |
2006 |
rs1057520040
|
1.000 |
0.160 |
19 |
1218449 |
missense variant |
A/G
|
snv
|
|
|
Peutz-Jeghers Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
1 |
1999 |
1999 |