List of variants in gene FGFR3 reported as pathogenic for benign neoplasm

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000142.5(FGFR3):c.1949A>C (p.Lys650Thr)	rs121913105	0.00001
NM_000142.5(FGFR3):c.1108G>T (p.Gly370Cys)	rs121913479
NM_000142.5(FGFR3):c.1138G>A (p.Gly380Arg)	rs28931614
NM_000142.5(FGFR3):c.1620C>G (p.Asn540Lys)	rs28933068
NM_000142.5(FGFR3):c.1949A>T (p.Lys650Met)	rs121913105
NM_000142.5(FGFR3):c.1950G>C (p.Lys650Asn)	rs28928868
NM_000142.5(FGFR3):c.2419T>A (p.Ter807Arg)	rs121913101
NM_000142.5(FGFR3):c.2420G>T (p.Ter807Leu)	rs397515514
NM_000142.5(FGFR3):c.742C>T (p.Arg248Cys)	rs121913482
NM_000142.5(FGFR3):c.746C>G (p.Ser249Cys)	rs121913483
NM_000142.5(FGFR3):c.749C>G (p.Pro250Arg)	rs4647924

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