ClinVar Miner

List of variants in gene FGFR3 reported as benign by PreventionGenetics,PreventionGenetics

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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_000142.4(FGFR3):c.1075+30G>C rs3135886
NM_000142.4(FGFR3):c.1075+5C>T rs3135885
NM_000142.4(FGFR3):c.1076-13C>T rs114754024
NM_000142.4(FGFR3):c.1076-16G>A rs3135889
NM_000142.4(FGFR3):c.1267-32C>T rs3135890
NM_000142.4(FGFR3):c.1535-8G>T rs111460786
NM_000142.4(FGFR3):c.1959+22G>A rs3135898
NM_000142.4(FGFR3):c.445+3A>G rs3135868
NM_000142.4(FGFR3):c.615+8C>G rs17878375
NM_000142.4(FGFR3):c.616-40T>C rs2305183
NM_000142.5(FGFR3):c.1014C>T (p.Thr338=) rs4647928
NM_000142.5(FGFR3):c.1345C>T (p.Pro449Ser) rs61735104
NM_000142.5(FGFR3):c.1647G>T (p.Gly549=) rs3135897
NM_000142.5(FGFR3):c.169G>A (p.Val57Met) rs61735064
NM_000142.5(FGFR3):c.2205C>G (p.Pro735=) rs145020302
NM_000142.5(FGFR3):c.348C>T (p.Arg116=) rs2305179
NM_000142.5(FGFR3):c.417C>T (p.Asp139=) rs3135867
NM_000142.5(FGFR3):c.588C>T (p.Arg196=) rs2305180
NM_000142.5(FGFR3):c.603T>C (p.Ile201=) rs2305181
NM_000142.5(FGFR3):c.882T>C (p.Asn294=) rs2234909

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