ClinVar Miner

List of variants in gene FGFR3 reported as benign by Invitae

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Gene type:
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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_000142.5(FGFR3):c.1953G>A (p.Thr651=) rs7688609 0.95729
NM_000142.5(FGFR3):c.882T>C (p.Asn294=) rs2234909 0.20412
NM_000142.5(FGFR3):c.445+3A>G rs3135868 0.09950
NM_000142.5(FGFR3):c.603T>C (p.Ile201=) rs2305181 0.09854
NM_000142.5(FGFR3):c.417C>T (p.Asp139=) rs3135867 0.03551
NM_000142.5(FGFR3):c.588C>T (p.Arg196=) rs2305180 0.03125
NM_000142.5(FGFR3):c.615+8C>G rs17878375 0.02283
NM_000142.5(FGFR3):c.1076-17C>T rs17881967 0.02051
NM_000142.5(FGFR3):c.348C>T (p.Arg116=) rs2305179 0.01752
NM_000142.5(FGFR3):c.1075+5C>T rs3135885 0.01659
NM_000142.5(FGFR3):c.1345C>T (p.Pro449Ser) rs61735104 0.00867
NM_000142.5(FGFR3):c.654G>C (p.Val218=) rs147769045 0.00703
NM_000142.5(FGFR3):c.1076-13C>T rs114754024 0.00661
NM_000142.5(FGFR3):c.1645+15G>A rs192433202 0.00533
NM_000142.5(FGFR3):c.616-15C>T rs17883683 0.00494
NM_000142.5(FGFR3):c.663G>A (p.Ser221=) rs114421370 0.00485
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656 0.00342
NM_000142.5(FGFR3):c.1535-8G>T rs111460786 0.00332
NM_000142.5(FGFR3):c.1014C>T (p.Thr338=) rs4647928 0.00328
NM_000142.5(FGFR3):c.1076-16G>A rs3135889 0.00296
NM_000142.5(FGFR3):c.393G>A (p.Ser131=) rs55662109 0.00292
NM_000142.5(FGFR3):c.2205C>G (p.Pro735=) rs145020302 0.00287
NM_000142.5(FGFR3):c.1535-20G>A rs113557371 0.00174
NM_000142.5(FGFR3):c.1959+15G>C rs17886888 0.00158
NM_000142.5(FGFR3):c.678C>T (p.Tyr226=) rs141575580 0.00142
NM_000142.5(FGFR3):c.1413-16C>G rs201702411 0.00114
NM_000142.5(FGFR3):c.2169-5C>T rs17884617 0.00112
NM_000142.5(FGFR3):c.739+15G>T rs373101038 0.00108
NM_000142.5(FGFR3):c.1497C>T (p.Ala499=) rs140594137 0.00106
NM_000142.5(FGFR3):c.2043G>A (p.Gly681=) rs17883356 0.00101
NM_000142.5(FGFR3):c.193G>A (p.Gly65Arg) rs2305178 0.00097
NM_000142.5(FGFR3):c.990C>T (p.Thr330=) rs2305185 0.00097
NM_000142.5(FGFR3):c.1349C>T (p.Thr450Met) rs56240927 0.00083
NM_000142.5(FGFR3):c.1923C>T (p.Asp641=) rs148104605 0.00081
NM_000142.5(FGFR3):c.1646-4C>T rs200428838 0.00054
NM_000142.5(FGFR3):c.446-17C>T rs376137178 0.00053
NM_000142.5(FGFR3):c.2088C>T (p.Pro696=) rs142884145 0.00052
NM_000142.5(FGFR3):c.1023G>A (p.Ala341=) rs147833498 0.00050
NM_000142.5(FGFR3):c.1959+8C>T rs371666188 0.00048
NM_000142.5(FGFR3):c.1686C>T (p.Asn562=) rs761445231 0.00046
NM_000142.5(FGFR3):c.252G>A (p.Ser84=) rs367973461 0.00039
NM_000142.5(FGFR3):c.713G>A (p.Arg238Gln) rs199944818 0.00037
NM_000142.5(FGFR3):c.130G>A (p.Gly44Ser) rs146080119 0.00036
NM_000142.5(FGFR3):c.446-5C>T rs144211980 0.00021
NM_000142.5(FGFR3):c.771G>A (p.Ala257=) rs138334098 0.00021
NM_000142.5(FGFR3):c.490C>G (p.Leu164Val) rs577990843 0.00020
NM_000142.5(FGFR3):c.933G>A (p.Thr311=) rs142805104 0.00015
NM_000142.5(FGFR3):c.1449C>T (p.Phe483=) rs545617229 0.00014
NM_000142.5(FGFR3):c.930+10C>T rs534857289 0.00014
NM_000142.5(FGFR3):c.616-18G>C rs372940259 0.00013
NM_000142.5(FGFR3):c.1413-20C>T rs367942098 0.00011
NM_000142.5(FGFR3):c.1960-13C>T rs377604726 0.00011
NM_000142.5(FGFR3):c.1719G>A (p.Pro573=) rs772157613 0.00010
NM_000142.5(FGFR3):c.1227C>T (p.Pro409=) rs533316478 0.00008
NM_000142.5(FGFR3):c.639G>A (p.Leu213=) rs138707520 0.00007
NM_000142.5(FGFR3):c.1287G>A (p.Ala429=) rs187229103 0.00006
NM_000142.5(FGFR3):c.684C>T (p.Cys228=) rs769248723 0.00003
NM_000142.5(FGFR3):c.1935C>T (p.Leu645=) rs104886006 0.00002
NM_000142.5(FGFR3):c.1290C>T (p.Ser430=) rs3135891 0.00001
NM_000142.5(FGFR3):c.1668G>A (p.Glu556=) rs1388294342 0.00001
NM_000142.5(FGFR3):c.1075+11CTG[6]
NM_000142.5(FGFR3):c.1218G>C (p.Leu406=)
NM_000142.5(FGFR3):c.1647G>T (p.Gly549=) rs3135897
NM_000142.5(FGFR3):c.1837-20_1837-9dup
NM_000142.5(FGFR3):c.1959+11C>T
NM_000142.5(FGFR3):c.2275-8G>A
NM_000142.5(FGFR3):c.615+6C>A rs2305182
NM_000142.5(FGFR3):c.912C>G (p.Pro304=) rs201012537

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