| Variant | Gene | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|
|
0.700 | GeneticVariation | UNIPROT | Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia. | 15996210 | 2005 |
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|
0.700 | GeneticVariation | UNIPROT | Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. | 12792735 | 2004 |
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|
0.700 | GeneticVariation | UNIPROT | Microsatellite instability and mutation analysis among southern Italian patients with colorectal carcinoma: detection of different alterations accounting for MLH1 and MSH2 inactivation in familial cases. | 14504054 | 2004 |
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|
0.700 | GeneticVariation | UNIPROT | Microsatellite instability and mutation analysis among southern Italian patients with colorectal carcinoma: detection of different alterations accounting for MLH1 and MSH2 inactivation in familial cases. | 14504054 | 2004 |
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|
0.700 | GeneticVariation | UNIPROT | Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. | 12792735 | 2004 |
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|
0.700 | GeneticVariation | UNIPROT | Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. | 12792735 | 2004 |
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|
0.700 | GeneticVariation | UNIPROT | Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. | 12792735 | 2004 |
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|
0.700 | GeneticVariation | UNIPROT | Mutator phenotypes of common polymorphisms and missense mutations in MSH2. | 10469597 | 1999 |
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|
0.700 | GeneticVariation | UNIPROT | Molecular nature of colon tumors in hereditary nonpolyposis colon cancer, familial polyposis, and sporadic colon cancer. | 8690195 | 1996 |
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|
0.700 | GeneticVariation | UNIPROT | ||||||
|
0.700 | GeneticVariation | UNIPROT | ||||||
|
0.700 | GeneticVariation | UNIPROT |