List of variants in gene FGFR3 reported as uncertain significance for not specified

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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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000142.5(FGFR3):c.158G>C (p.Ser53Thr)	rs201433984	0.00014
NM_000142.5(FGFR3):c.2028C>T (p.Asp676=)	rs754598297	0.00004
NM_000142.5(FGFR3):c.2417C>T (p.Thr806Met)	rs374547489	0.00004
NM_000142.5(FGFR3):c.1537G>A (p.Asp513Asn)	rs121913112	0.00002
NM_000142.5(FGFR3):c.1056G>A (p.Ala352=)	rs765849160	0.00001
NM_000142.5(FGFR3):c.1331C>T (p.Ser444Phe)	rs761325047	0.00001
NM_000142.5(FGFR3):c.1756G>A (p.Glu586Lys)	rs576023546	0.00001
NM_000142.5(FGFR3):c.370C>T (p.Arg124Trp)	rs199740841	0.00001
NC_000004.11:g.(?_1795019)_(1795771_1800980)dup
NM_000142.5(FGFR3):c.109G>A (p.Glu37Lys)	rs1553842213
NM_000142.5(FGFR3):c.1316G>C (p.Arg439Pro)
NM_000142.5(FGFR3):c.1411dup (p.Arg471fs)
NM_000142.5(FGFR3):c.1549A>G (p.Lys517Glu)
NM_000142.5(FGFR3):c.1630G>T (p.Ala544Ser)
NM_000142.5(FGFR3):c.1657G>A (p.Val553Met)	rs199544087
NM_000142.5(FGFR3):c.2031-4G>A
NM_000142.5(FGFR3):c.2334del (p.Ser779fs)
NM_000142.5(FGFR3):c.2374dup (p.Asp792fs)	rs1057518205

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