ClinVar Miner

Submissions for variant NM_006231.4(POLE):c.857C>A (p.Pro286His)

dbSNP: rs1057519943
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000428894 SCV000507156 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000439138 SCV000507157 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000417898 SCV000507158 likely pathogenic Pancreatic adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000428131 SCV000507159 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438366 SCV000507160 likely pathogenic Uterine carcinosarcoma 2016-05-31 no assertion criteria provided literature only

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