ClinVar Miner

Submissions for variant NM_002755.4(MAP2K1):c.157T>A (p.Phe53Ile)

dbSNP: rs1057519728
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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) RCV000431446 SCV000506684 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000442281 SCV000506685 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421374 SCV000506686 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432046 SCV000506687 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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