ClinVar Miner

Submissions for variant NM_023110.2(FGFR1):c.1543A>G (p.Met515Val) (rs1057519899)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000435727 SCV000506381 likely pathogenic Astrocytoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000418590 SCV000506382 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429290 SCV000506383 likely pathogenic Brainstem glioma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436467 SCV000506384 likely pathogenic Neuroblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419230 SCV000506385 likely pathogenic Adenocarcinoma of stomach 2016-05-31 no assertion criteria provided literature only

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