ClinVar Miner

List of variants in gene FMO3 studied for not provided

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Gene type:
ClinVar version:
Total variants: 138
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HGVS dbSNP gnomAD frequency
NM_001002294.3(FMO3):c.855C>T (p.Asn285=) rs909530 0.31712
NM_001002294.3(FMO3):c.1183+35T>C rs909531 0.24203
NM_001002294.3(FMO3):c.923A>G (p.Glu308Gly) rs2266780 0.14140
NM_001002294.3(FMO3):c.769G>A (p.Val257Met) rs1736557 0.06174
NM_001002294.3(FMO3):c.830T>C (p.Val277Ala) rs2066530 0.01554
NM_001002294.3(FMO3):c.1084G>C (p.Glu362Gln) rs2066532 0.00425
NM_001002294.3(FMO3):c.321+31C>A rs2066537 0.00418
NM_001002294.3(FMO3):c.1221T>C (p.Asn407=) rs79553697 0.00376
NM_001002294.3(FMO3):c.1079T>C (p.Leu360Pro) rs28363581 0.00158
NM_001002294.3(FMO3):c.1530C>T (p.Phe510=) rs28363595 0.00070
NM_001002294.3(FMO3):c.1505T>G (p.Val502Gly) rs60306057 0.00061
NM_001002294.3(FMO3):c.1250G>A (p.Arg417His) rs200985584 0.00037
NM_001002294.3(FMO3):c.913G>T (p.Glu305Ter) rs61753344 0.00035
NM_001002294.3(FMO3):c.906C>T (p.Asn302=) rs2066536 0.00031
NM_001002294.3(FMO3):c.1222G>T (p.Asp408Tyr) rs141280604 0.00029
NM_001002294.3(FMO3):c.341A>G (p.Asn114Ser) rs186763441 0.00029
NM_001002294.3(FMO3):c.1204A>G (p.Met402Val) rs141117096 0.00021
NM_001002294.3(FMO3):c.1474C>T (p.Arg492Trp) rs72549334 0.00019
NM_001002294.3(FMO3):c.329T>C (p.Val110Ala) rs376881697 0.00019
NM_001002294.3(FMO3):c.172G>A (p.Val58Ile) rs144935285 0.00016
NM_001002294.3(FMO3):c.1322T>C (p.Ile441Thr) rs535435928 0.00013
NM_001002294.3(FMO3):c.660G>A (p.Val220=) rs373775407 0.00013
NM_001002294.3(FMO3):c.628-6T>C rs369396459 0.00010
NM_001002294.3(FMO3):c.225C>T (p.Pro75=) rs141235954 0.00008
NM_001002294.3(FMO3):c.1302G>A (p.Met434Ile) rs72549332 0.00007
NM_001002294.3(FMO3):c.929C>T (p.Ser310Leu) rs572292275 0.00006
NM_001002294.3(FMO3):c.706G>A (p.Val236Ile) rs201271626 0.00004
NM_001002294.3(FMO3):c.132+13T>C rs371276117 0.00003
NM_001002294.3(FMO3):c.1160G>A (p.Arg387His) rs72549331 0.00002
NM_001002294.3(FMO3):c.1479G>A (p.Ser493=) rs766383334 0.00001
NM_001002294.3(FMO3):c.1539T>C (p.His513=) rs771817026 0.00001
NM_001002294.3(FMO3):c.684T>C (p.Gly228=) rs934652609 0.00001
NM_001002294.3(FMO3):c.713G>A (p.Arg238Gln) rs748324481 0.00001
NM_001002294.3(FMO3):c.979T>G (p.Phe327Val) rs767834931 0.00001
NC_000001.10:g.(?_171061800)_(171061951_?)del
NC_000001.10:g.(?_171061800)_(171073134_?)del
NC_000001.10:g.(?_171061800)_(171086582_?)del
NC_000001.10:g.(?_171072906)_(171080158_?)dup
NC_000001.10:g.(?_171076796)_(171086582_?)del
NC_000001.10:g.(?_171083127)_(171083522_?)del
NM_001002294.3(FMO3):c.1005C>A (p.Tyr335Ter)
NM_001002294.3(FMO3):c.102dup (p.Asn35fs)
NM_001002294.3(FMO3):c.1041C>T (p.Asn347=)
NM_001002294.3(FMO3):c.1045G>T (p.Glu349Ter)
NM_001002294.3(FMO3):c.1050C>T (p.Ile350=)
NM_001002294.3(FMO3):c.10A>T (p.Lys4Ter)
NM_001002294.3(FMO3):c.1104G>A (p.Val368=)
NM_001002294.3(FMO3):c.1118dup (p.Ser374fs)
NM_001002294.3(FMO3):c.1131T>G (p.Ala377=)
NM_001002294.3(FMO3):c.1139_1140del (p.Pro380fs) rs775064534
NM_001002294.3(FMO3):c.1183+10T>C
NM_001002294.3(FMO3):c.1183+12A>G
NM_001002294.3(FMO3):c.1183+1del
NM_001002294.3(FMO3):c.1183+20C>T
NM_001002294.3(FMO3):c.1184-2A>G
NM_001002294.3(FMO3):c.1184-5A>G
NM_001002294.3(FMO3):c.1184-9_1184-6del
NM_001002294.3(FMO3):c.1210del (p.Asp404fs)
NM_001002294.3(FMO3):c.1231G>T (p.Glu411Ter)
NM_001002294.3(FMO3):c.1237dup (p.Met413fs)
NM_001002294.3(FMO3):c.1245A>G (p.Lys415=)
NM_001002294.3(FMO3):c.1256+10C>T
NM_001002294.3(FMO3):c.1256+20T>C
NM_001002294.3(FMO3):c.1257-6C>T
NM_001002294.3(FMO3):c.1257-7T>C
NM_001002294.3(FMO3):c.1257G>A (p.Trp419Ter)
NM_001002294.3(FMO3):c.1262G>T (p.Gly421Val)
NM_001002294.3(FMO3):c.1269C>T (p.Ser423=)
NM_001002294.3(FMO3):c.1275C>T (p.Thr425=)
NM_001002294.3(FMO3):c.1284A>G (p.Thr428=)
NM_001002294.3(FMO3):c.1293T>C (p.Ile431=)
NM_001002294.3(FMO3):c.1311C>T (p.Leu437=)
NM_001002294.3(FMO3):c.132+11T>C
NM_001002294.3(FMO3):c.132+12G>A
NM_001002294.3(FMO3):c.132+15G>C
NM_001002294.3(FMO3):c.132+1G>T rs886038576
NM_001002294.3(FMO3):c.132+9C>G
NM_001002294.3(FMO3):c.133-11T>C
NM_001002294.3(FMO3):c.133-11_133-10del
NM_001002294.3(FMO3):c.133-2A>G
NM_001002294.3(FMO3):c.133-9C>T
NM_001002294.3(FMO3):c.1425C>T (p.Gly475=)
NM_001002294.3(FMO3):c.1478C>T (p.Ser493Leu)
NM_001002294.3(FMO3):c.1498C>T (p.Arg500Ter)
NM_001002294.3(FMO3):c.1506C>T (p.Val502=)
NM_001002294.3(FMO3):c.151A>G (p.Arg51Gly)
NM_001002294.3(FMO3):c.1551C>T (p.Leu517=)
NM_001002294.3(FMO3):c.1557A>G (p.Ala519=)
NM_001002294.3(FMO3):c.1569G>T (p.Leu523=)
NM_001002294.3(FMO3):c.1575C>T (p.Ile525=)
NM_001002294.3(FMO3):c.16del (p.Ala6fs)
NM_001002294.3(FMO3):c.170C>G (p.Ser57Ter)
NM_001002294.3(FMO3):c.174_175insA (p.Phe59fs)
NM_001002294.3(FMO3):c.1A>G (p.Met1Val)
NM_001002294.3(FMO3):c.209C>T (p.Pro70Leu)
NM_001002294.3(FMO3):c.21C>T (p.Ile7=)
NM_001002294.3(FMO3):c.22_29del (p.Ile8fs)
NM_001002294.3(FMO3):c.237del (p.Asn80fs)
NM_001002294.3(FMO3):c.321+1G>T
NM_001002294.3(FMO3):c.322-6T>C
NM_001002294.3(FMO3):c.322-8T>C
NM_001002294.3(FMO3):c.42C>T (p.Gly14=)
NM_001002294.3(FMO3):c.628-1G>A
NM_001002294.3(FMO3):c.628-2A>G
NM_001002294.3(FMO3):c.668G>A (p.Arg223Gln)
NM_001002294.3(FMO3):c.674_690del (p.Trp225fs)
NM_001002294.3(FMO3):c.692G>A (p.Trp231Ter)
NM_001002294.3(FMO3):c.700C>T (p.Leu234=)
NM_001002294.3(FMO3):c.712C>A (p.Arg238=)
NM_001002294.3(FMO3):c.712C>T (p.Arg238Ter)
NM_001002294.3(FMO3):c.726_729del (p.Phe242fs)
NM_001002294.3(FMO3):c.744G>A (p.Pro248=)
NM_001002294.3(FMO3):c.762G>A (p.Trp254Ter)
NM_001002294.3(FMO3):c.768C>T (p.Tyr256=)
NM_001002294.3(FMO3):c.768_769insAGATGACTG (p.Val257delinsArgTer)
NM_001002294.3(FMO3):c.775C>T (p.Gln259Ter)
NM_001002294.3(FMO3):c.778A>G (p.Met260Val)
NM_001002294.3(FMO3):c.807T>C (p.Tyr269=)
NM_001002294.3(FMO3):c.81G>A (p.Glu27=)
NM_001002294.3(FMO3):c.825_827+16del
NM_001002294.3(FMO3):c.827+17C>A
NM_001002294.3(FMO3):c.827+17C>T
NM_001002294.3(FMO3):c.827+18G>A
NM_001002294.3(FMO3):c.827+19T>C
NM_001002294.3(FMO3):c.827+9G>A
NM_001002294.3(FMO3):c.828-12T>C
NM_001002294.3(FMO3):c.828-13G>C
NM_001002294.3(FMO3):c.839_842dup (p.Pro282fs)
NM_001002294.3(FMO3):c.859G>T (p.Glu287Ter) rs1057520649
NM_001002294.3(FMO3):c.885C>T (p.Gly295=)
NM_001002294.3(FMO3):c.894C>T (p.Ser298=)
NM_001002294.3(FMO3):c.900G>A (p.Lys300=)
NM_001002294.3(FMO3):c.912G>A (p.Lys304=)
NM_001002294.3(FMO3):c.930G>A (p.Ser310=)
NM_001002294.3(FMO3):c.951C>T (p.Thr317=)
NM_001002294.3(FMO3):c.969C>T (p.Asp323=) rs115908652
NM_001002294.3(FMO3):c.987A>C (p.Thr329=)
NM_001002294.3(FMO3):c.993_994del (p.Tyr331_Ser332delinsTer) rs751356173

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