rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis.
|
11788572 |
2002 |
rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
A CGC>CAT gene conversion-like event resulting in the R122H mutation in the cationic trypsinogen gene and its implication in the genotyping of pancreatitis.
|
11073545 |
2000 |
rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation.
|
10930381 |
2000 |
rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis.
|
10204851 |
1999 |
rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
Heterozygosity for the A16V mutation is strongly associated with CP.
|
10381903 |
1999 |
rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
Mutations of the cationic trypsinogen in hereditary pancreatitis.
|
9633818 |
1998 |
rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis.
|
9322498 |
1997 |
rs202003805
|
|
|
0.840 |
GeneticVariation |
UNIPROT |
Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.
|
8841182 |
1996 |
rs111033567
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl.
|
15776435 |
2005 |
rs111033568
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl.
|
15776435 |
2005 |
rs387906698
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl.
|
15776435 |
2005 |
rs111033567
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Interaction between trypsinogen isoforms in genetically determined pancreatitis: mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2).
|
14695529 |
2004 |
rs111033568
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Interaction between trypsinogen isoforms in genetically determined pancreatitis: mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2).
|
14695529 |
2004 |
rs387906698
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Interaction between trypsinogen isoforms in genetically determined pancreatitis: mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2).
|
14695529 |
2004 |
rs111033567
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis.
|
11788572 |
2002 |
rs111033567
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants.
|
11866271 |
2002 |
rs111033568
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis.
|
11788572 |
2002 |
rs111033568
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants.
|
11866271 |
2002 |
rs387906698
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis.
|
11788572 |
2002 |
rs387906698
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Mutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants.
|
11866271 |
2002 |
rs111033567
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
A CGC>CAT gene conversion-like event resulting in the R122H mutation in the cationic trypsinogen gene and its implication in the genotyping of pancreatitis.
|
11073545 |
2000 |
rs111033567
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation.
|
10930381 |
2000 |
rs111033568
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation.
|
10930381 |
2000 |
rs111033568
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
A CGC>CAT gene conversion-like event resulting in the R122H mutation in the cationic trypsinogen gene and its implication in the genotyping of pancreatitis.
|
11073545 |
2000 |
rs387906698
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Chronic pancreatitis associated with an activation peptide mutation that facilitates trypsin activation.
|
10930381 |
2000 |