ClinVar Miner

Submissions for variant NM_004448.4(ERBB2):c.2329G>A (p.Val777Met)

dbSNP: rs121913471
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000439665 SCV000506118 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422009 SCV000506119 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000428744 SCV000506120 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only

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