ClinVar Miner

Submissions for variant NM_000142.5(FGFR3):c.2089G>T (p.Gly697Cys)

dbSNP: rs121913480
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000417814 SCV000505532 likely pathogenic Urinary bladder carcinoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440614 SCV000510409 likely pathogenic Carcinoma 2016-05-13 no assertion criteria provided literature only

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