ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.159T>G (p.Phe53Leu)

dbSNP: rs1057519908
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000436917 SCV000506676 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419468 SCV000506677 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000430169 SCV000506678 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440832 SCV000506679 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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