ClinVar Miner

Submissions for variant NM_181523.3(PIK3R1):c.1126G>C (p.Gly376Arg) (rs1057519757)

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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) RCV000435812 SCV000505007 likely pathogenic Neoplasm 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422432 SCV000507138 likely pathogenic Neoplasm of brain 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429204 SCV000507139 likely pathogenic Glioblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000439435 SCV000507140 likely pathogenic Uterine Carcinosarcoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421788 SCV000507141 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only

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