ClinVar Miner

Submissions for variant NM_000141.5(FGFR2):c.1145G>A (p.Cys382Tyr)

dbSNP: rs1057519900
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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) RCV000434751 SCV000506392 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438442 SCV000506393 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421261 SCV000506394 likely pathogenic Carcinoma of esophagus 2016-05-31 no assertion criteria provided literature only

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