FMO3 — 300 ClinVar variants
All ClinVar germline FMO3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 87 flagged for review →
33 Pathogenic · 18 Pathogenic/Likely pathogenic · 39 Likely pathogenic · 26 Conflicting · 7 Benign · 13 Benign/Likely benign · 91 Likely benign · 73 Uncertain significance
Full FMO3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 87
Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.
Predictors vs ClinVar 3
ClinVar calls these pathogenic, but the computational predictors lean tolerated — the highest-value review flag.
-
FMO3 p.Met260Val
Pathogenic/Likely pathogenic
Multiple submitters
trimethylaminuria
-
FMO3 p.Ser310Leu
Pathogenic/Likely pathogenic
Multiple submitters
trimethylaminuria
-
FMO3 p.Met434Ile
Likely pathogenic
Single submitter
trimethylaminuria
Predictors agree, ClinVar conflicts 11
ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.
- FMO3 p.Arg186His Conflicting Single submitter
-
FMO3 p.Arg387Leu
Conflicting
Single submitter
FMO3-related disorders
-
FMO3 p.Asn114Ser
Conflicting
Single submitter
trimethylaminuria
-
FMO3 p.Asp408Tyr
Conflicting
Single submitter
FMO3-related disorders
-
FMO3 p.Glu362Gln
Conflicting
Single submitter
trimethylaminuria
-
FMO3 p.Gly330Glu
Conflicting
Single submitter
trimethylaminuria
-
FMO3 p.Gly475Asp
Conflicting
Single submitter
FMO3-related disorders
-
FMO3 p.Met402Val
Conflicting
Single submitter
trimethylaminuria
-
FMO3 p.Val110Ala
Conflicting
Single submitter
trimethylaminuria
-
FMO3 p.Val187Gly
Conflicting
Single submitter
Inborn genetic diseases
-
FMO3 p.Val58Ile
Conflicting
Single submitter
trimethylaminuria
Predictors lean, ClinVar uncertain 50
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
-
FMO3 p.Phe327Val
Uncertain significance
Multiple submitters
trimethylaminuria
-
FMO3 p.Val143Glu
Uncertain significance
Multiple submitters
trimethylaminuria
-
FMO3 p.Ala10Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Ala138Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Ala378Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Ala458Val
Uncertain significance
Single submitter
Inborn genetic diseases
- FMO3 p.Arg483Thr Uncertain significance Single submitter
-
FMO3 p.Asn268Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Cys170Trp
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Cys324Ser
Uncertain significance
Single submitter
Inborn genetic diseases
- FMO3 p.Gln209His Uncertain significance Single submitter
-
FMO3 p.Gly14Asp
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Gly184Val
Uncertain significance
Single submitter
Inborn genetic diseases
- FMO3 p.Gly228Ser Uncertain significance Single submitter
- FMO3 p.Gly38Trp Uncertain significance Single submitter
-
FMO3 p.Gly503Arg
Uncertain significance
Single submitter
trimethylaminuria
-
FMO3 p.His266Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.His46Gln
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Ile212Leu
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Ile292Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Ile431Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Ile87Asn
Uncertain significance
Single submitter
trimethylaminuria
-
FMO3 p.Ile8Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Leu40Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Leu505Phe
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Lys102Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Lys354Glu
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Lys363Asn
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Lys516Glu
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Met144Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Met144Val
Uncertain significance
Single submitter
trimethylaminuria
-
FMO3 p.Met413Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Phe319Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Phe440Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Pro248Leu
Uncertain significance
Single submitter
trimethylaminuria
-
FMO3 p.Pro521Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Ser332Gly
Uncertain significance
Single submitter
trimethylaminuria
-
FMO3 p.Ser332Thr
Uncertain significance
Single submitter
Inborn genetic diseases
- FMO3 p.Thr201Ser Uncertain significance Single submitter
-
FMO3 p.Thr398Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Thr425Ile
Uncertain significance
Single submitter
Inborn genetic diseases
- FMO3 p.Thr428Ser Uncertain significance Single submitter
-
FMO3 p.Thr488Ala
Uncertain significance
Single submitter
trimethylaminuria
-
FMO3 p.Trp225Gly
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Trp479Gly
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Val12Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Val189Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Val224Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Val297Leu
Uncertain significance
Single submitter
trimethylaminuria
-
FMO3 p.Val474Leu
Uncertain significance
Single submitter
Inborn genetic diseases
Predictors split 23
The independent predictors disagree with each other — read with care.
-
FMO3 p.Asp132His
Benign
Multiple submitters
trimethylaminuria
-
FMO3 p.Glu308Gly
Benign/Likely benign
Multiple submitters
trimethylaminuria
-
FMO3 p.Gly421Val
Pathogenic/Likely pathogenic
Multiple submitters
trimethylaminuria
-
FMO3 p.Val502Gly
Likely benign
Multiple submitters
trimethylaminuria
-
FMO3 p.Ala367Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Ala52Thr
Uncertain significance
Single submitter
trimethylaminuria
-
FMO3 p.Arg205Cys
Conflicting
Single submitter
trimethylaminuria
- FMO3 p.Arg417Cys Conflicting Single submitter
-
FMO3 p.Arg417His
Conflicting
Single submitter
trimethylaminuria
-
FMO3 p.Arg500Gln
Conflicting
Single submitter
Inborn genetic diseases
-
FMO3 p.Asn84Asp
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Gly395Glu
Uncertain significance
Single submitter
Inborn genetic diseases
- FMO3 p.Ile199Thr Uncertain significance Single submitter
-
FMO3 p.Ile441Thr
Conflicting
Single submitter
trimethylaminuria
-
FMO3 p.Leu360Pro
Likely benign
Single submitter
trimethylaminuria
-
FMO3 p.Lys363Glu
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Met405Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Met66Ile
Likely pathogenic
Single submitter
trimethylaminuria
-
FMO3 p.Ser401Tyr
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Thr201Pro
Likely benign
Single submitter
trimethylaminuria
-
FMO3 p.Thr309Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Tyr335His
Uncertain significance
Single submitter
Inborn genetic diseases
-
FMO3 p.Ser17Phe
Uncertain significance
No assertion criteria
FMO3-related disorder
All FMO3 variants
Pathogenic 33
- p.Cys197_Asp198delinsTer Multiple submitters FMO3-related disorders
- p.Glu208Ter Multiple submitters trimethylaminuria
- p.Glu305Ter Multiple submitters FMO3-related disorders
- p.Ala120fs Single submitter
- p.Ala6fs Single submitter
- p.Asn194fs Single submitter
- p.Asn35fs Single submitter
- p.Asp404fs Single submitter
- p.Gln209Ter Single submitter
- p.Gln259Ter Single submitter
- p.Gln470Ter Single submitter trimethylaminuria
- p.Glu136Ter Single submitter
- p.Glu349Ter Single submitter
- p.Glu411Ter Single submitter
- p.Gly148Ter Single submitter
- p.Ile8fs Single submitter
- p.Leu163fs Single submitter
- p.Lys4Ter Single submitter
- p.Met1Val Single submitter
- p.Met413fs Single submitter
- p.Phe59fs Single submitter
- p.Pro153fs Single submitter trimethylaminuria
- p.Pro282fs Single submitter
- p.Pro70Leu Single submitter
- p.Ser57Ter Single submitter
- p.Trp225fs Single submitter
- p.Trp231Ter Single submitter
- p.Trp254Ter Single submitter
- p.Trp419Ter Single submitter
- p.Tyr335Ter Single submitter
- p.Val257delinsArgTer Single submitter
- p.Glu314Ter No assertion criteria trimethylaminuria
- p.Glu65fs No assertion criteria trimethylaminuria
Pathogenic/Likely pathogenic 18
- c.1183+1del Multiple submitters FMO3-related disorders
- p.Arg131fs Multiple submitters trimethylaminuria
- p.Arg238Gln Multiple submitters trimethylaminuria
- p.Arg238Ter Multiple submitters trimethylaminuria
- p.Arg492Trp Multiple submitters FMO3-related disorders
- p.Arg500Ter Multiple submitters trimethylaminuria
- p.Asn80fs Multiple submitters trimethylaminuria
- p.Gln124Ter Multiple submitters trimethylaminuria
- p.Glu287Ter Multiple submitters trimethylaminuria
- p.Gly421Val Multiple submitters trimethylaminuria ⚠
- p.Met260Val Multiple submitters trimethylaminuria ⚠
- p.Phe242fs Multiple submitters trimethylaminuria
- p.Pro153Leu Multiple submitters FMO3-related disorders
- p.Pro380fs Multiple submitters trimethylaminuria
- p.Ser310Leu Multiple submitters trimethylaminuria ⚠
- p.Ser374fs Multiple submitters trimethylaminuria
- p.Tyr331_Ser332delinsTer Multiple submitters trimethylaminuria
- p.Val187fs Multiple submitters trimethylaminuria
Likely pathogenic 39
- c.484+2T>G Multiple submitters trimethylaminuria
- c.828-2A>G Multiple submitters trimethylaminuria
- p.Arg223Gln Multiple submitters trimethylaminuria
- p.Arg223Trp Multiple submitters FMO3-related disorders
- p.Asn61Ser Multiple submitters trimethylaminuria
- p.Gly191Cys Multiple submitters trimethylaminuria
- c.1184-2A>G Single submitter
- c.132+1G>A Single submitter trimethylaminuria
- c.133-2A>G Single submitter
- c.321+1G>T Single submitter
- c.484+1G>A Single submitter
- c.628-1G>A Single submitter
- c.628-2A>G Single submitter
- c.825_827+16del Single submitter
- c.828-2A>T Single submitter trimethylaminuria
- p.Ala52fs Single submitter trimethylaminuria
- p.Arg387Cys Single submitter trimethylaminuria
- p.Arg387Gly Single submitter trimethylaminuria
- p.Arg51Gly Single submitter
- p.Asn227fs Single submitter trimethylaminuria
- p.Asp232Tyr Single submitter
- p.Gln88Ter Single submitter trimethylaminuria
- p.Glu281Ter Single submitter trimethylaminuria
- p.Glu32Lys Single submitter trimethylaminuria
- p.Glu436Ter Single submitter trimethylaminuria
- p.Gly148Arg Single submitter trimethylaminuria
- p.Leu40fs Single submitter trimethylaminuria
- p.Lys416fs Single submitter trimethylaminuria
- p.Met1Ile Single submitter trimethylaminuria
- p.Met434Ile Single submitter trimethylaminuria ⚠
- p.Met66Ile Single submitter trimethylaminuria ⚠
- p.Phe109fs Single submitter trimethylaminuria
- p.Phe140Ser Single submitter trimethylaminuria
- p.Ser195Leu Single submitter trimethylaminuria
- p.Trp125Ter Single submitter trimethylaminuria
- p.Trp388Ter Single submitter trimethylaminuria
- p.Tyr256Ter Single submitter trimethylaminuria
- c.132+1G>T No assertion criteria
- p.Leu293fs No assertion criteria FMO3-related disorder
Conflicting classifications of pathogenicity 26
- c.132+13T>C Single submitter trimethylaminuria
- c.628-6T>C Single submitter trimethylaminuria
- c.-25G>A Single submitter trimethylaminuria
- p.Arg186His Single submitter ⚠
- p.Arg205Cys Single submitter trimethylaminuria ⚠
- p.Arg387His Single submitter trimethylaminuria
- p.Arg387Leu Single submitter FMO3-related disorders ⚠
- p.Arg417Cys Single submitter ⚠
- p.Arg417His Single submitter trimethylaminuria ⚠
- p.Arg500Gln Single submitter Inborn genetic diseases ⚠
- p.Asn114Ser Single submitter trimethylaminuria ⚠
- p.Asp408Tyr Single submitter FMO3-related disorders ⚠
- p.Glu362Gln Single submitter trimethylaminuria ⚠
- p.Gly228= Single submitter trimethylaminuria
- p.Gly330Glu Single submitter trimethylaminuria ⚠
- p.Gly475Asp Single submitter FMO3-related disorders ⚠
- p.His513= Single submitter trimethylaminuria
- p.Ile441Thr Single submitter trimethylaminuria ⚠
- p.Met402Val Single submitter trimethylaminuria ⚠
- p.Met82Thr Single submitter trimethylaminuria
- p.Phe510= Single submitter trimethylaminuria
- p.Pro75= Single submitter trimethylaminuria
- p.Val110Ala Single submitter trimethylaminuria ⚠
- p.Val187Gly Single submitter Inborn genetic diseases ⚠
- p.Val220= Single submitter trimethylaminuria
- p.Val58Ile Single submitter trimethylaminuria ⚠
Benign 7
- c.1183+35T>C Multiple submitters
- c.485-22G>A Multiple submitters trimethylaminuria
- p.Asp132His Multiple submitters trimethylaminuria ⚠
- p.Val257Met Multiple submitters trimethylaminuria
- c.1184-32dup Single submitter
- p.Asn183= Single submitter
- p.Gly295= Single submitter
Benign/Likely benign 13
- c.627+10C>G Multiple submitters trimethylaminuria
- c.827+19T>C Multiple submitters
- p.Asn285= Multiple submitters trimethylaminuria
- p.Asn407= Multiple submitters trimethylaminuria
- p.Asp323= Multiple submitters trimethylaminuria
- p.Glu158Lys Multiple submitters trimethylaminuria
- p.Glu308Gly Multiple submitters trimethylaminuria ⚠
- p.Gly180Val Multiple submitters trimethylaminuria
- p.Ile350= Multiple submitters
- p.Ser147= Multiple submitters trimethylaminuria
- p.Ser195= Multiple submitters trimethylaminuria
- p.Val236Ile Multiple submitters trimethylaminuria
- p.Val277Ala Multiple submitters trimethylaminuria
Likely benign 91
- c.321+31C>A Multiple submitters
- p.Asn302= Multiple submitters
- p.Ser493= Multiple submitters
- p.Thr532Ile Multiple submitters Inborn genetic diseases
- p.Val502Gly Multiple submitters trimethylaminuria ⚠
- c.1183+10T>C Single submitter
- c.1183+12A>G Single submitter
- c.1183+20C>T Single submitter
- c.1184-5A>G Single submitter
- c.1184-9_1184-6del Single submitter
- c.1256+10C>A Single submitter
- c.1256+10C>T Single submitter
- c.1256+20T>C Single submitter
- c.1257-6C>G Single submitter
- c.1257-6C>T Single submitter
- c.1257-7T>C Single submitter
- c.132+11T>C Single submitter
- c.132+12G>A Single submitter
- c.132+15G>C Single submitter
- c.132+9C>G Single submitter
- c.133-11_133-10del Single submitter
- c.133-11T>C Single submitter
- c.133-17A>G Single submitter
- c.133-9C>T Single submitter
- c.321+44_321+46del Single submitter
- c.321+7T>C Single submitter
- c.322-6T>C Single submitter
- c.322-8T>C Single submitter
- c.485-19T>C Single submitter
- c.627+10C>T Single submitter
- c.627+11C>T Single submitter
- c.627+12C>T Single submitter
- c.627+15G>A Single submitter
- c.627+20C>T Single submitter
- c.627+9C>T Single submitter
- c.827+17C>A Single submitter
- c.827+17C>T Single submitter
- c.827+18G>A Single submitter
- c.827+9G>A Single submitter
- c.828-12T>C Single submitter
- c.828-13G>C Single submitter
- c.828-14T>C Single submitter
- c.828-15_828-14del Single submitter
- p.Ala120= Single submitter
- p.Ala377= Single submitter
- p.Ala519= Single submitter
- p.Arg131= Single submitter
- p.Arg238= Single submitter
- p.Asn347= Single submitter
- p.Asp198Glu Single submitter
- p.Glu27= Single submitter
- p.Gly123= Single submitter
- p.Gly14= Single submitter
- p.Gly148= Single submitter
- p.Gly25= Single submitter
- p.Gly475= Single submitter
- p.Ile431= Single submitter
- p.Ile525= Single submitter
- p.Ile7= Single submitter
- p.Leu234= Single submitter
- p.Leu360Pro Single submitter trimethylaminuria ⚠
- p.Leu437= Single submitter
- p.Leu517= Single submitter
- p.Leu523= Single submitter
- p.Lys300= Single submitter
- p.Lys304= Single submitter
- p.Lys33Arg Single submitter Inborn genetic diseases
- p.Lys415= Single submitter
- p.Lys456= Single submitter
- p.Pro156= Single submitter
- p.Pro179= Single submitter
- p.Pro248= Single submitter
- p.Ser137= Single submitter
- p.Ser173= Single submitter
- p.Ser298= Single submitter
- p.Ser310= Single submitter
- p.Ser423= Single submitter
- p.Ser439= Single submitter
- p.Ser493Leu Single submitter
- p.Thr128= Single submitter
- p.Thr201Pro Single submitter trimethylaminuria ⚠
- p.Thr317= Single submitter
- p.Thr329= Single submitter
- p.Thr425= Single submitter
- p.Thr428= Single submitter
- p.Tyr256= Single submitter
- p.Tyr269= Single submitter
- p.Val189= Single submitter
- p.Val368= Single submitter
- p.Val502= Single submitter
- c.133-2658A>T No assertion criteria FMO3-related disorder
Uncertain significance 73
- p.Phe327Val Multiple submitters trimethylaminuria ⚠
- p.Tyr430His Multiple submitters Inborn genetic diseases
- p.Val143Glu Multiple submitters trimethylaminuria ⚠
- c.484+13T>C Single submitter trimethylaminuria
- c.627+13G>A Single submitter trimethylaminuria
- c.-6-1G>C Single submitter
- c.*261A>G Single submitter trimethylaminuria
- c.*364C>T Single submitter trimethylaminuria
- c.*374A>G Single submitter trimethylaminuria
- c.*4T>C Single submitter trimethylaminuria
- c.*52G>A Single submitter trimethylaminuria
- p.Ala10Val Single submitter Inborn genetic diseases ⚠
- p.Ala138Thr Single submitter Inborn genetic diseases ⚠
- p.Ala367Val Single submitter Inborn genetic diseases ⚠
- p.Ala378Val Single submitter Inborn genetic diseases ⚠
- p.Ala458Val Single submitter Inborn genetic diseases ⚠
- p.Ala52Thr Single submitter trimethylaminuria ⚠
- p.Arg483Thr Single submitter ⚠
- p.Asn268Ser Single submitter Inborn genetic diseases ⚠
- p.Asn84Asp Single submitter Inborn genetic diseases ⚠
- p.Cys170Trp Single submitter Inborn genetic diseases ⚠
- p.Cys324Ser Single submitter Inborn genetic diseases ⚠
- p.Gln209His Single submitter ⚠
- p.Gly14Asp Single submitter Inborn genetic diseases ⚠
- p.Gly184Val Single submitter Inborn genetic diseases ⚠
- p.Gly228Ser Single submitter ⚠
- p.Gly38Trp Single submitter ⚠
- p.Gly395Glu Single submitter Inborn genetic diseases ⚠
- p.Gly503Arg Single submitter trimethylaminuria ⚠
- p.His266Arg Single submitter Inborn genetic diseases ⚠
- p.His46Gln Single submitter Inborn genetic diseases ⚠
- p.Ile199Thr Single submitter ⚠
- p.Ile212Leu Single submitter Inborn genetic diseases ⚠
- p.Ile292Val Single submitter Inborn genetic diseases ⚠
- p.Ile431Val Single submitter Inborn genetic diseases ⚠
- p.Ile87Asn Single submitter trimethylaminuria ⚠
- p.Ile8Val Single submitter Inborn genetic diseases ⚠
- p.Leu243= Single submitter trimethylaminuria
- p.Leu40Val Single submitter Inborn genetic diseases ⚠
- p.Leu505Phe Single submitter Inborn genetic diseases ⚠
- p.Lys102Arg Single submitter Inborn genetic diseases ⚠
- p.Lys354Glu Single submitter Inborn genetic diseases ⚠
- p.Lys363Asn Single submitter Inborn genetic diseases ⚠
- p.Lys363Glu Single submitter Inborn genetic diseases ⚠
- p.Lys516Glu Single submitter Inborn genetic diseases ⚠
- p.Met144Ile Single submitter Inborn genetic diseases ⚠
- p.Met144Val Single submitter trimethylaminuria ⚠
- p.Met405Val Single submitter Inborn genetic diseases ⚠
- p.Met413Ile Single submitter Inborn genetic diseases ⚠
- p.Phe319Ser Single submitter Inborn genetic diseases ⚠
- p.Phe440Ser Single submitter Inborn genetic diseases ⚠
- p.Pro248Leu Single submitter trimethylaminuria ⚠
- p.Pro521Ser Single submitter Inborn genetic diseases ⚠
- p.Ser332Gly Single submitter trimethylaminuria ⚠
- p.Ser332Thr Single submitter Inborn genetic diseases ⚠
- p.Ser401Tyr Single submitter Inborn genetic diseases ⚠
- p.Thr201Ser Single submitter ⚠
- p.Thr307Pro Single submitter
- p.Thr309Ile Single submitter Inborn genetic diseases ⚠
- p.Thr398Ala Single submitter Inborn genetic diseases ⚠
- p.Thr425Ile Single submitter Inborn genetic diseases ⚠
- p.Thr428Ser Single submitter ⚠
- p.Thr488Ala Single submitter trimethylaminuria ⚠
- p.Trp225Gly Single submitter Inborn genetic diseases ⚠
- p.Trp479Gly Single submitter Inborn genetic diseases ⚠
- p.Tyr335His Single submitter Inborn genetic diseases ⚠
- p.Val12Ala Single submitter Inborn genetic diseases ⚠
- p.Val189Ala Single submitter Inborn genetic diseases ⚠
- p.Val190Phe Single submitter
- p.Val224Ala Single submitter Inborn genetic diseases ⚠
- p.Val297Leu Single submitter trimethylaminuria ⚠
- p.Val474Leu Single submitter Inborn genetic diseases ⚠
- p.Ser17Phe No assertion criteria FMO3-related disorder ⚠