Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.13717504C>ACA3201604DNAH5c.12516G>T (p.Leu4172=)
c.12471G>T (p.Leu4157=)
c.12624G>T (p.Leu4208=)
c.11529G>T (p.Leu3843=)
c.7713G>T (p.Leu2571=)
c.7266G>T (p.Leu2422=)
c.6603G>T (p.Leu2201=)
c.11118G>T (p.Leu3706=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
5g.13717504C=CA1528407080DNAH5c.12516G= (p.Leu4172=)
c.12471G= (p.Leu4157=)
c.12624G= (p.Leu4208=)
c.11529G= (p.Leu3843=)
c.7713G= (p.Leu2571=)
c.7266G= (p.Leu2422=)
c.6603G= (p.Leu2201=)
c.11118G= (p.Leu3706=)
5g.13717504C>GCA443254964DNAH5c.12516G>C (p.Leu4172=)
c.12471G>C (p.Leu4157=)
c.12624G>C (p.Leu4208=)
c.11529G>C (p.Leu3843=)
c.7713G>C (p.Leu2571=)
c.7266G>C (p.Leu2422=)
c.6603G>C (p.Leu2201=)
c.11118G>C (p.Leu3706=)
dbSNP gnomAD v4
5g.13717504C>TCA443254965DNAH5c.12516G>A (p.Leu4172=)
c.12471G>A (p.Leu4157=)
c.12624G>A (p.Leu4208=)
c.11529G>A (p.Leu3843=)
c.7713G>A (p.Leu2571=)
c.7266G>A (p.Leu2422=)
c.6603G>A (p.Leu2201=)
c.11118G>A (p.Leu3706=)
5g.13717505A>CCA359208398DNAH5c.12515T>G (p.Leu4172Arg)
c.12470T>G (p.Leu4157Arg)
c.12623T>G (p.Leu4208Arg)
c.11528T>G (p.Leu3843Arg)
c.7712T>G (p.Leu2571Arg)
c.7265T>G (p.Leu2422Arg)
c.6602T>G (p.Leu2201Arg)
c.11117T>G (p.Leu3706Arg)
5g.13717505A>GCA359208399DNAH5c.12515T>C (p.Leu4172Pro)
c.12470T>C (p.Leu4157Pro)
c.12623T>C (p.Leu4208Pro)
c.11528T>C (p.Leu3843Pro)
c.7712T>C (p.Leu2571Pro)
c.7265T>C (p.Leu2422Pro)
c.6602T>C (p.Leu2201Pro)
c.11117T>C (p.Leu3706Pro)
5g.13717505A>TCA359208397DNAH5c.12515T>A (p.Leu4172Gln)
c.12470T>A (p.Leu4157Gln)
c.12623T>A (p.Leu4208Gln)
c.11528T>A (p.Leu3843Gln)
c.7712T>A (p.Leu2571Gln)
c.7265T>A (p.Leu2422Gln)
c.6602T>A (p.Leu2201Gln)
c.11117T>A (p.Leu3706Gln)
5g.13717506G>ACA443254970DNAH5c.12514C>T (p.Leu4172=)
c.12469C>T (p.Leu4157=)
c.12622C>T (p.Leu4208=)
c.11527C>T (p.Leu3843=)
c.7711C>T (p.Leu2571=)
c.7264C>T (p.Leu2422=)
c.6601C>T (p.Leu2201=)
c.11116C>T (p.Leu3706=)
5g.13717506G>CCA359208400DNAH5c.12514C>G (p.Leu4172Val)
c.12469C>G (p.Leu4157Val)
c.12622C>G (p.Leu4208Val)
c.11527C>G (p.Leu3843Val)
c.7711C>G (p.Leu2571Val)
c.7264C>G (p.Leu2422Val)
c.6601C>G (p.Leu2201Val)
c.11116C>G (p.Leu3706Val)
5g.13717506G>TCA359208403DNAH5c.12514C>A (p.Leu4172Met)
c.12469C>A (p.Leu4157Met)
c.12622C>A (p.Leu4208Met)
c.11527C>A (p.Leu3843Met)
c.7711C>A (p.Leu2571Met)
c.7264C>A (p.Leu2422Met)
c.6601C>A (p.Leu2201Met)
c.11116C>A (p.Leu3706Met)
5g.13717507G>ACA113919302DNAH5c.12513C>T (p.Asp4171=)
c.12468C>T (p.Asp4156=)
c.12621C>T (p.Asp4207=)
c.11526C>T (p.Asp3842=)
c.7710C>T (p.Asp2570=)
c.7263C>T (p.Asp2421=)
c.6600C>T (p.Asp2200=)
c.11115C>T (p.Asp3705=)
ClinVar dbSNP
5g.13717507G>CCA359208409DNAH5c.12513C>G (p.Asp4171Glu)
c.12468C>G (p.Asp4156Glu)
c.12621C>G (p.Asp4207Glu)
c.11526C>G (p.Asp3842Glu)
c.7710C>G (p.Asp2570Glu)
c.7263C>G (p.Asp2421Glu)
c.6600C>G (p.Asp2200Glu)
c.11115C>G (p.Asp3705Glu)
ClinVar
5g.13717507G=CA1528407081DNAH5c.12513C= (p.Asp4171=)
c.12468C= (p.Asp4156=)
c.12621C= (p.Asp4207=)
c.11526C= (p.Asp3842=)
c.7710C= (p.Asp2570=)
c.7263C= (p.Asp2421=)
c.6600C= (p.Asp2200=)
c.11115C= (p.Asp3705=)
5g.13717507G>TCA3201605DNAH5c.12513C>A (p.Asp4171Glu)
c.12468C>A (p.Asp4156Glu)
c.12621C>A (p.Asp4207Glu)
c.11526C>A (p.Asp3842Glu)
c.7710C>A (p.Asp2570Glu)
c.7263C>A (p.Asp2421Glu)
c.6600C>A (p.Asp2200Glu)
c.11115C>A (p.Asp3705Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.13717508T>ACA359208410DNAH5c.12512A>T (p.Asp4171Val)
c.12467A>T (p.Asp4156Val)
c.12620A>T (p.Asp4207Val)
c.11525A>T (p.Asp3842Val)
c.7709A>T (p.Asp2570Val)
c.7262A>T (p.Asp2421Val)
c.6599A>T (p.Asp2200Val)
c.11114A>T (p.Asp3705Val)
5g.13717508T>CCA359208413DNAH5c.12512A>G (p.Asp4171Gly)
c.12467A>G (p.Asp4156Gly)
c.12620A>G (p.Asp4207Gly)
c.11525A>G (p.Asp3842Gly)
c.7709A>G (p.Asp2570Gly)
c.7262A>G (p.Asp2421Gly)
c.6599A>G (p.Asp2200Gly)
c.11114A>G (p.Asp3705Gly)
5g.13717508T>GCA359208417DNAH5c.12512A>C (p.Asp4171Ala)
c.12467A>C (p.Asp4156Ala)
c.12620A>C (p.Asp4207Ala)
c.11525A>C (p.Asp3842Ala)
c.7709A>C (p.Asp2570Ala)
c.7262A>C (p.Asp2421Ala)
c.6599A>C (p.Asp2200Ala)
c.11114A>C (p.Asp3705Ala)
5g.13717509C>ACA359208425DNAH5c.12511G>T (p.Asp4171Tyr)
c.12466G>T (p.Asp4156Tyr)
c.12619G>T (p.Asp4207Tyr)
c.11524G>T (p.Asp3842Tyr)
c.7708G>T (p.Asp2570Tyr)
c.7261G>T (p.Asp2421Tyr)
c.6598G>T (p.Asp2200Tyr)
c.11113G>T (p.Asp3705Tyr)
5g.13717509C>GCA359208429DNAH5c.12511G>C (p.Asp4171His)
c.12466G>C (p.Asp4156His)
c.12619G>C (p.Asp4207His)
c.11524G>C (p.Asp3842His)
c.7708G>C (p.Asp2570His)
c.7261G>C (p.Asp2421His)
c.6598G>C (p.Asp2200His)
c.11113G>C (p.Asp3705His)
5g.13717509C>TCA359208431DNAH5c.12511G>A (p.Asp4171Asn)
c.12466G>A (p.Asp4156Asn)
c.12619G>A (p.Asp4207Asn)
c.11524G>A (p.Asp3842Asn)
c.7708G>A (p.Asp2570Asn)
c.7261G>A (p.Asp2421Asn)
c.6598G>A (p.Asp2200Asn)
c.11113G>A (p.Asp3705Asn)
gnomAD v4
5g.13717510T>ACA359208435DNAH5c.12510A>T (p.Gln4170His)
c.12465A>T (p.Gln4155His)
c.12618A>T (p.Gln4206His)
c.11523A>T (p.Gln3841His)
c.7707A>T (p.Gln2569His)
c.7260A>T (p.Gln2420His)
c.6597A>T (p.Gln2199His)
c.11112A>T (p.Gln3704His)
5g.13717510T>CCA443254984DNAH5c.12510A>G (p.Gln4170=)
c.12465A>G (p.Gln4155=)
c.12618A>G (p.Gln4206=)
c.11523A>G (p.Gln3841=)
c.7707A>G (p.Gln2569=)
c.7260A>G (p.Gln2420=)
c.6597A>G (p.Gln2199=)
c.11112A>G (p.Gln3704=)
5g.13717510T>GCA359208438DNAH5c.12510A>C (p.Gln4170His)
c.12465A>C (p.Gln4155His)
c.12618A>C (p.Gln4206His)
c.11523A>C (p.Gln3841His)
c.7707A>C (p.Gln2569His)
c.7260A>C (p.Gln2420His)
c.6597A>C (p.Gln2199His)
c.11112A>C (p.Gln3704His)
5g.13717511delCA2739274570DNAH5c.12510del (p.Asp4171ThrfsTer5)
c.12465del (p.Asp4156ThrfsTer5)
c.12618del (p.Asp4207ThrfsTer5)
c.11523del (p.Asp3842ThrfsTer5)
c.7707del (p.Asp2570ThrfsTer5)
c.7260del (p.Asp2421ThrfsTer5)
c.6597del (p.Asp2200ThrfsTer5)
c.11112del (p.Asp3705ThrfsTer5)
ClinVar
5g.13717511T>ACA359208444DNAH5c.12509A>T (p.Gln4170Leu)
c.12464A>T (p.Gln4155Leu)
c.12617A>T (p.Gln4206Leu)
c.11522A>T (p.Gln3841Leu)
c.7706A>T (p.Gln2569Leu)
c.7259A>T (p.Gln2420Leu)
c.6596A>T (p.Gln2199Leu)
c.11111A>T (p.Gln3704Leu)
5g.13717511T>CCA359208446DNAH5c.12509A>G (p.Gln4170Arg)
c.12464A>G (p.Gln4155Arg)
c.12617A>G (p.Gln4206Arg)
c.11522A>G (p.Gln3841Arg)
c.7706A>G (p.Gln2569Arg)
c.7259A>G (p.Gln2420Arg)
c.6596A>G (p.Gln2199Arg)
c.11111A>G (p.Gln3704Arg)
gnomAD v4
5g.13717511T>GCA359208448DNAH5c.12509A>C (p.Gln4170Pro)
c.12464A>C (p.Gln4155Pro)
c.12617A>C (p.Gln4206Pro)
c.11522A>C (p.Gln3841Pro)
c.7706A>C (p.Gln2569Pro)
c.7259A>C (p.Gln2420Pro)
c.6596A>C (p.Gln2199Pro)
c.11111A>C (p.Gln3704Pro)
5g.13717512G>ACA359208470DNAH5c.12508C>T (p.Gln4170Ter)
c.12463C>T (p.Gln4155Ter)
c.12616C>T (p.Gln4206Ter)
c.11521C>T (p.Gln3841Ter)
c.7705C>T (p.Gln2569Ter)
c.7258C>T (p.Gln2420Ter)
c.6595C>T (p.Gln2199Ter)
c.11110C>T (p.Gln3704Ter)
5g.13717512G>CCA359208465DNAH5c.12508C>G (p.Gln4170Glu)
c.12463C>G (p.Gln4155Glu)
c.12616C>G (p.Gln4206Glu)
c.11521C>G (p.Gln3841Glu)
c.7705C>G (p.Gln2569Glu)
c.7258C>G (p.Gln2420Glu)
c.6595C>G (p.Gln2199Glu)
c.11110C>G (p.Gln3704Glu)
5g.13717512G>TCA359208458DNAH5c.12508C>A (p.Gln4170Lys)
c.12463C>A (p.Gln4155Lys)
c.12616C>A (p.Gln4206Lys)
c.11521C>A (p.Gln3841Lys)
c.7705C>A (p.Gln2569Lys)
c.7258C>A (p.Gln2420Lys)
c.6595C>A (p.Gln2199Lys)
c.11110C>A (p.Gln3704Lys)
5g.13717513G>ACA443254991DNAH5c.12507C>T (p.Ser4169=)
c.12462C>T (p.Ser4154=)
c.12615C>T (p.Ser4205=)
c.11520C>T (p.Ser3840=)
c.7704C>T (p.Ser2568=)
c.7257C>T (p.Ser2419=)
c.6594C>T (p.Ser2198=)
c.11109C>T (p.Ser3703=)
5g.13717513G>CCA359208472DNAH5c.12507C>G (p.Ser4169Arg)
c.12462C>G (p.Ser4154Arg)
c.12615C>G (p.Ser4205Arg)
c.11520C>G (p.Ser3840Arg)
c.7704C>G (p.Ser2568Arg)
c.7257C>G (p.Ser2419Arg)
c.6594C>G (p.Ser2198Arg)
c.11109C>G (p.Ser3703Arg)
5g.13717513G>TCA359208477DNAH5c.12507C>A (p.Ser4169Arg)
c.12462C>A (p.Ser4154Arg)
c.12615C>A (p.Ser4205Arg)
c.11520C>A (p.Ser3840Arg)
c.7704C>A (p.Ser2568Arg)
c.7257C>A (p.Ser2419Arg)
c.6594C>A (p.Ser2198Arg)
c.11109C>A (p.Ser3703Arg)
5g.13717514C>ACA359208480DNAH5c.12506G>T (p.Ser4169Ile)
c.12461G>T (p.Ser4154Ile)
c.12614G>T (p.Ser4205Ile)
c.11519G>T (p.Ser3840Ile)
c.7703G>T (p.Ser2568Ile)
c.7256G>T (p.Ser2419Ile)
c.6593G>T (p.Ser2198Ile)
c.11108G>T (p.Ser3703Ile)
gnomAD v4
5g.13717514C>GCA359208482DNAH5c.12506G>C (p.Ser4169Thr)
c.12461G>C (p.Ser4154Thr)
c.12614G>C (p.Ser4205Thr)
c.11519G>C (p.Ser3840Thr)
c.7703G>C (p.Ser2568Thr)
c.7256G>C (p.Ser2419Thr)
c.6593G>C (p.Ser2198Thr)
c.11108G>C (p.Ser3703Thr)
5g.13717514C>TCA359208485DNAH5c.12506G>A (p.Ser4169Asn)
c.12461G>A (p.Ser4154Asn)
c.12614G>A (p.Ser4205Asn)
c.11519G>A (p.Ser3840Asn)
c.7703G>A (p.Ser2568Asn)
c.7256G>A (p.Ser2419Asn)
c.6593G>A (p.Ser2198Asn)
c.11108G>A (p.Ser3703Asn)
5g.13717515T>ACA359208489DNAH5c.12505A>T (p.Ser4169Cys)
c.12460A>T (p.Ser4154Cys)
c.12613A>T (p.Ser4205Cys)
c.11518A>T (p.Ser3840Cys)
c.7702A>T (p.Ser2568Cys)
c.7255A>T (p.Ser2419Cys)
c.6592A>T (p.Ser2198Cys)
c.11107A>T (p.Ser3703Cys)
dbSNP gnomAD v2
5g.13717515T>CCA359208494DNAH5c.12505A>G (p.Ser4169Gly)
c.12460A>G (p.Ser4154Gly)
c.12613A>G (p.Ser4205Gly)
c.11518A>G (p.Ser3840Gly)
c.7702A>G (p.Ser2568Gly)
c.7255A>G (p.Ser2419Gly)
c.6592A>G (p.Ser2198Gly)
c.11107A>G (p.Ser3703Gly)
5g.13717515T>GCA359208499DNAH5c.12505A>C (p.Ser4169Arg)
c.12460A>C (p.Ser4154Arg)
c.12613A>C (p.Ser4205Arg)
c.11518A>C (p.Ser3840Arg)
c.7702A>C (p.Ser2568Arg)
c.7255A>C (p.Ser2419Arg)
c.6592A>C (p.Ser2198Arg)
c.11107A>C (p.Ser3703Arg)
5g.13717515T=CA1528407082DNAH5c.12505A= (p.Ser4169=)
c.12460A= (p.Ser4154=)
c.12613A= (p.Ser4205=)
c.11518A= (p.Ser3840=)
c.7702A= (p.Ser2568=)
c.7255A= (p.Ser2419=)
c.6592A= (p.Ser2198=)
c.11107A= (p.Ser3703=)
5g.13717516G>ACA443254994DNAH5c.12504C>T (p.Val4168=)
c.12459C>T (p.Val4153=)
c.12612C>T (p.Val4204=)
c.11517C>T (p.Val3839=)
c.7701C>T (p.Val2567=)
c.7254C>T (p.Val2418=)
c.6591C>T (p.Val2197=)
c.11106C>T (p.Val3702=)
5g.13717516G>CCA443254995DNAH5c.12504C>G (p.Val4168=)
c.12459C>G (p.Val4153=)
c.12612C>G (p.Val4204=)
c.11517C>G (p.Val3839=)
c.7701C>G (p.Val2567=)
c.7254C>G (p.Val2418=)
c.6591C>G (p.Val2197=)
c.11106C>G (p.Val3702=)
5g.13717516G>TCA443254997DNAH5c.12504C>A (p.Val4168=)
c.12459C>A (p.Val4153=)
c.12612C>A (p.Val4204=)
c.11517C>A (p.Val3839=)
c.7701C>A (p.Val2567=)
c.7254C>A (p.Val2418=)
c.6591C>A (p.Val2197=)
c.11106C>A (p.Val3702=)
5g.13717517A>CCA359208503DNAH5c.12503T>G (p.Val4168Gly)
c.12458T>G (p.Val4153Gly)
c.12611T>G (p.Val4204Gly)
c.11516T>G (p.Val3839Gly)
c.7700T>G (p.Val2567Gly)
c.7253T>G (p.Val2418Gly)
c.6590T>G (p.Val2197Gly)
c.11105T>G (p.Val3702Gly)
5g.13717517A>GCA359208506DNAH5c.12503T>C (p.Val4168Ala)
c.12458T>C (p.Val4153Ala)
c.12611T>C (p.Val4204Ala)
c.11516T>C (p.Val3839Ala)
c.7700T>C (p.Val2567Ala)
c.7253T>C (p.Val2418Ala)
c.6590T>C (p.Val2197Ala)
c.11105T>C (p.Val3702Ala)
gnomAD v4
5g.13717517A>TCA359208511DNAH5c.12503T>A (p.Val4168Asp)
c.12458T>A (p.Val4153Asp)
c.12611T>A (p.Val4204Asp)
c.11516T>A (p.Val3839Asp)
c.7700T>A (p.Val2567Asp)
c.7253T>A (p.Val2418Asp)
c.6590T>A (p.Val2197Asp)
c.11105T>A (p.Val3702Asp)
5g.13717518C>ACA359208516DNAH5c.12502G>T (p.Val4168Phe)
c.12457G>T (p.Val4153Phe)
c.12610G>T (p.Val4204Phe)
c.11515G>T (p.Val3839Phe)
c.7699G>T (p.Val2567Phe)
c.7252G>T (p.Val2418Phe)
c.6589G>T (p.Val2197Phe)
c.11104G>T (p.Val3702Phe)
gnomAD v4
5g.13717518C=CA1528407083DNAH5c.12502G= (p.Val4168=)
c.12457G= (p.Val4153=)
c.12610G= (p.Val4204=)
c.11515G= (p.Val3839=)
c.7699G= (p.Val2567=)
c.7252G= (p.Val2418=)
c.6589G= (p.Val2197=)
c.11104G= (p.Val3702=)
5g.13717518C>GCA359208519DNAH5c.12502G>C (p.Val4168Leu)
c.12457G>C (p.Val4153Leu)
c.12610G>C (p.Val4204Leu)
c.11515G>C (p.Val3839Leu)
c.7699G>C (p.Val2567Leu)
c.7252G>C (p.Val2418Leu)
c.6589G>C (p.Val2197Leu)
c.11104G>C (p.Val3702Leu)
5g.13717518C>TCA3201606DNAH5c.12502G>A (p.Val4168Ile)
c.12457G>A (p.Val4153Ile)
c.12610G>A (p.Val4204Ile)
c.11515G>A (p.Val3839Ile)
c.7699G>A (p.Val2567Ile)
c.7252G>A (p.Val2418Ile)
c.6589G>A (p.Val2197Ile)
c.11104G>A (p.Val3702Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched