ClinVar Miner

List of variants in gene FGFR3 reported as benign for not specified

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Total variants: 37
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HGVS dbSNP
NM_000142.4(FGFR3):c.-102-3T>C rs10023340
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.1076-17C>T rs17881967
NM_000142.4(FGFR3):c.109+26G>A rs17884282
NM_000142.4(FGFR3):c.1267-32C>T rs3135890
NM_000142.4(FGFR3):c.1535-20G>A rs113557371
NM_000142.4(FGFR3):c.1535-8G>T rs111460786
NM_000142.4(FGFR3):c.1645+15G>A rs192433202
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.616-15C>T rs17883683
NM_000142.4(FGFR3):c.616-40T>C rs2305183
NM_000142.4(FGFR3):c.930+72C>G rs2305184
NM_000142.5(FGFR3):c.*5C>G rs17879364
NM_000142.5(FGFR3):c.1014C>T (p.Thr338=) rs4647928
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656
NM_000142.5(FGFR3):c.1345C>T (p.Pro449Ser) rs61735104
NM_000142.5(FGFR3):c.1349C>T (p.Thr450Met) rs56240927
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.1953= (p.Thr651=) rs7688609
NM_000142.5(FGFR3):c.2043G>A (p.Gly681=) rs17883356
NM_000142.5(FGFR3):c.2088C>T (p.Pro696=) rs142884145
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.393G>A (p.Ser131=) rs55662109
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.654G>C (p.Val218=) rs147769045
NM_000142.5(FGFR3):c.663G>A (p.Ser221=) rs114421370
NM_000142.5(FGFR3):c.678C>T (p.Tyr226=) rs141575580
NM_000142.5(FGFR3):c.882T>C (p.Asn294=) rs2234909

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