ClinVar Miner

Submissions for variant NM_000141.5(FGFR2):c.1647T>G (p.Asn549Lys)

dbSNP: rs121913476
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000434110 SCV000505184 likely pathogenic Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation 2014-12-26 no assertion criteria provided literature only

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