rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer.
|
29577179 |
2019 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing.
|
28873162 |
2017 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Roles for E-cadherin cell surface regulation in cancer.
|
27582386 |
2016 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Roles for E-cadherin cell surface regulation in cancer.
|
27582386 |
2016 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond.
|
26182300 |
2015 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Searching for E-cadherin gene mutations in early onset diffuse gastric cancer and hereditary diffuse gastric cancer in Korean patients.
|
23264079 |
2013 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Searching for E-cadherin gene mutations in early onset diffuse gastric cancer and hereditary diffuse gastric cancer in Korean patients.
|
23264079 |
2013 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
To accomplish our objective we characterized the effect of eleven HDGC CDH1 germline missense mutations (T118R, L214P, G239R, A298T, T340A, P373L, R749W, E757K, E781D, P799R and V832M) on cell motility.
|
19268661 |
2009 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
CausalMutation
|
CLINVAR |
To accomplish our objective we characterized the effect of eleven HDGC CDH1 germline missense mutations (T118R, L214P, G239R, A298T, T340A, P373L, R749W, E757K, E781D, P799R and V832M) on cell motility.
|
19268661 |
2009 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer.
|
17545690 |
2007 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Identification of seven novel germline mutations in the human E-cadherin (CDH1) gene.
|
17221870 |
2007 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer.
|
17545690 |
2007 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Identification of seven novel germline mutations in the human E-cadherin (CDH1) gene.
|
17221870 |
2007 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
CausalMutation
|
CLINVAR |
A short guide to hereditary diffuse gastric cancer.
|
19725995 |
2007 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
A model to infer the pathogenic significance of CDH1 germline missense variants.
|
16924464 |
2006 |
rs587780537
|
|
Hereditary Diffuse Gastric Cancer
|
A |
0.700 |
CausalMutation
|
CLINVAR |
A model to infer the pathogenic significance of CDH1 germline missense variants.
|
16924464 |
2006 |