Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.21816506_21816507insGTATTTACACA2514662296DNAH11c.10372_10373insGTATTTACA (p.Ser3457_Met3458insSerIleTyr)
c.10393_10394insGTATTTACA (p.Ser3464_Met3465insSerIleTyr)
7g.21816506A=CA1693666200DNAH11c.10372A= (p.Met3458=)
c.10393A= (p.Met3465=)
7g.21816506A>CCA366948122DNAH11c.10372A>C (p.Met3458Leu)
c.10393A>C (p.Met3465Leu)
7g.21816506A>GCA4182346DNAH11c.10372A>G (p.Met3458Val)
c.10393A>G (p.Met3465Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816506A>TCA366948126DNAH11c.10372A>T (p.Met3458Leu)
c.10393A>T (p.Met3465Leu)
7g.21816507T>ACA366948131DNAH11c.10373T>A (p.Met3458Lys)
c.10394T>A (p.Met3465Lys)
dbSNP gnomAD v2 gnomAD v4
7g.21816507T>CCA366948134DNAH11c.10373T>C (p.Met3458Thr)
c.10394T>C (p.Met3465Thr)
gnomAD v4
7g.21816507T>GCA366948133DNAH11c.10373T>G (p.Met3458Arg)
c.10394T>G (p.Met3465Arg)
7g.21816507T=CA1693666203DNAH11c.10373T= (p.Met3458=)
c.10394T= (p.Met3465=)
7g.21816508G>ACA4182347DNAH11c.10374G>A (p.Met3458Ile)
c.10395G>A (p.Met3465Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.21816508G>CCA366948137DNAH11c.10374G>C (p.Met3458Ile)
c.10395G>C (p.Met3465Ile)
7g.21816508G=CA1693666208DNAH11c.10374G= (p.Met3458=)
c.10395G= (p.Met3465=)
7g.21816508G>TCA366948139DNAH11c.10374G>T (p.Met3458Ile)
c.10395G>T (p.Met3465Ile)
7g.21816509T>ACA366948141DNAH11c.10375T>A (p.Leu3459Met)
c.10396T>A (p.Leu3466Met)
7g.21816509T>CCA453966574DNAH11c.10375T>C (p.Leu3459=)
c.10396T>C (p.Leu3466=)
7g.21816509T>GCA366948144DNAH11c.10375T>G (p.Leu3459Val)
c.10396T>G (p.Leu3466Val)
7g.21816510T>ACA366948147DNAH11c.10376T>A (p.Leu3459Ter)
c.10397T>A (p.Leu3466Ter)
gnomAD v4
7g.21816510T>CCA366948150DNAH11c.10376T>C (p.Leu3459Ser)
c.10397T>C (p.Leu3466Ser)
gnomAD v4
7g.21816510T>GCA366948151DNAH11c.10376T>G (p.Leu3459Trp)
c.10397T>G (p.Leu3466Trp)
7g.21816511G>ACA453966577DNAH11c.10377G>A (p.Leu3459=)
c.10398G>A (p.Leu3466=)
ClinVar dbSNP gnomAD v3 gnomAD v4
7g.21816511G>CCA366948153DNAH11c.10377G>C (p.Leu3459Phe)
c.10398G>C (p.Leu3466Phe)
7g.21816511G=CA1693666212DNAH11c.10377G= (p.Leu3459=)
c.10398G= (p.Leu3466=)
7g.21816511G>TCA366948156DNAH11c.10377G>T (p.Leu3459Phe)
c.10398G>T (p.Leu3466Phe)
7g.21816512A>CCA366948166DNAH11c.10378A>C (p.Thr3460Pro)
c.10399A>C (p.Thr3467Pro)
7g.21816512A>GCA366948163DNAH11c.10378A>G (p.Thr3460Ala)
c.10399A>G (p.Thr3467Ala)
7g.21816512A>TCA366948160DNAH11c.10378A>T (p.Thr3460Ser)
c.10399A>T (p.Thr3467Ser)
7g.21816513C>ACA4182348DNAH11c.10379C>A (p.Thr3460Lys)
c.10400C>A (p.Thr3467Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816513C=CA1693666217DNAH11c.10379C= (p.Thr3460=)
c.10400C= (p.Thr3467=)
7g.21816513C>GCA366948172DNAH11c.10379C>G (p.Thr3460Arg)
c.10400C>G (p.Thr3467Arg)
7g.21816513C>TCA4182349DNAH11c.10379C>T (p.Thr3460Met)
c.10400C>T (p.Thr3467Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816514G>ACA4182350DNAH11c.10380G>A (p.Thr3460=)
c.10401G>A (p.Thr3467=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
7g.21816514G>CCA453966578DNAH11c.10380G>C (p.Thr3460=)
c.10401G>C (p.Thr3467=)
7g.21816514G=CA1693666222DNAH11c.10380G= (p.Thr3460=)
c.10401G= (p.Thr3467=)
7g.21816514G>TCA453966579DNAH11c.10380G>T (p.Thr3460=)
c.10401G>T (p.Thr3467=)
dbSNP gnomAD v4
7g.21816515G>ACA366948195DNAH11c.10381G>A (p.Asp3461Asn)
c.10402G>A (p.Asp3468Asn)
ClinVar dbSNP
7g.21816515G>CCA366948178DNAH11c.10381G>C (p.Asp3461His)
c.10402G>C (p.Asp3468His)
7g.21816515G=CA1693666228DNAH11c.10381G= (p.Asp3461=)
c.10402G= (p.Asp3468=)
7g.21816515G>TCA366948192DNAH11c.10381G>T (p.Asp3461Tyr)
c.10402G>T (p.Asp3468Tyr)
7g.21816516A>CCA366948199DNAH11c.10382A>C (p.Asp3461Ala)
c.10403A>C (p.Asp3468Ala)
7g.21816516A>GCA366948202DNAH11c.10382A>G (p.Asp3461Gly)
c.10403A>G (p.Asp3468Gly)
7g.21816516A>TCA366948203DNAH11c.10382A>T (p.Asp3461Val)
c.10403A>T (p.Asp3468Val)
gnomAD v4
7g.21816517T>ACA366948205DNAH11c.10383T>A (p.Asp3461Glu)
c.10404T>A (p.Asp3468Glu)
COSMIC COSMIC
7g.21816517T>CCA453966581DNAH11c.10383T>C (p.Asp3461=)
c.10404T>C (p.Asp3468=)
ClinVar dbSNP
7g.21816517T>GCA366948209DNAH11c.10383T>G (p.Asp3461Glu)
c.10404T>G (p.Asp3468Glu)
7g.21816517T=CA1693666233DNAH11c.10383T= (p.Asp3461=)
c.10404T= (p.Asp3468=)
7g.21816518G>ACA366948210DNAH11c.10384G>A (p.Asp3462Asn)
c.10405G>A (p.Asp3469Asn)
dbSNP
7g.21816518G>CCA366948213DNAH11c.10384G>C (p.Asp3462His)
c.10405G>C (p.Asp3469His)
7g.21816518G=CA1693666236DNAH11c.10384G= (p.Asp3462=)
c.10405G= (p.Asp3469=)
7g.21816518G>TCA366948216DNAH11c.10384G>T (p.Asp3462Tyr)
c.10405G>T (p.Asp3469Tyr)
COSMIC
7g.21816519A>CCA366948221DNAH11c.10385A>C (p.Asp3462Ala)
c.10406A>C (p.Asp3469Ala)
7g.21816519A>GCA366948220DNAH11c.10385A>G (p.Asp3462Gly)
c.10406A>G (p.Asp3469Gly)
7g.21816519A>TCA366948218DNAH11c.10385A>T (p.Asp3462Val)
c.10406A>T (p.Asp3469Val)
7g.21816520T>ACA366948223DNAH11c.10386T>A (p.Asp3462Glu)
c.10407T>A (p.Asp3469Glu)
7g.21816520T>CCA4182351DNAH11c.10386T>C (p.Asp3462=)
c.10407T>C (p.Asp3469=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816520T>GCA366948225DNAH11c.10386T>G (p.Asp3462Glu)
c.10407T>G (p.Asp3469Glu)
dbSNP
7g.21816520T=CA1693666239DNAH11c.10386T= (p.Asp3462=)
c.10407T= (p.Asp3469=)
7g.21816521G>ACA4182352DNAH11c.10387G>A (p.Ala3463Thr)
c.10408G>A (p.Ala3470Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816521G>CCA366948228DNAH11c.10387G>C (p.Ala3463Pro)
c.10408G>C (p.Ala3470Pro)
7g.21816521G=CA1693666242DNAH11c.10387G= (p.Ala3463=)
c.10408G= (p.Ala3470=)
7g.21816521G>TCA366948229DNAH11c.10387G>T (p.Ala3463Ser)
c.10408G>T (p.Ala3470Ser)
7g.21816522C>ACA366948232DNAH11c.10388C>A (p.Ala3463Asp)
c.10409C>A (p.Ala3470Asp)
7g.21816522C>GCA366948233DNAH11c.10388C>G (p.Ala3463Gly)
c.10409C>G (p.Ala3470Gly)
7g.21816522C>TCA366948234DNAH11c.10388C>T (p.Ala3463Val)
c.10409C>T (p.Ala3470Val)
gnomAD v4
7g.21816523T>ACA453966586DNAH11c.10389T>A (p.Ala3463=)
c.10410T>A (p.Ala3470=)
7g.21816523T>CCA453966584DNAH11c.10389T>C (p.Ala3463=)
c.10410T>C (p.Ala3470=)
dbSNP gnomAD v3 gnomAD v4
7g.21816523T>GCA453966585DNAH11c.10389T>G (p.Ala3463=)
c.10410T>G (p.Ala3470=)
7g.21816523T=CA1693666246DNAH11c.10389T= (p.Ala3463=)
c.10410T= (p.Ala3470=)
7g.21816524A=CA1693666248DNAH11c.10390A= (p.Thr3464=)
c.10411A= (p.Thr3471=)
7g.21816524A>CCA366948235DNAH11c.10390A>C (p.Thr3464Pro)
c.10411A>C (p.Thr3471Pro)
7g.21816524A>GCA366948236DNAH11c.10390A>G (p.Thr3464Ala)
c.10411A>G (p.Thr3471Ala)
dbSNP gnomAD v2 gnomAD v4
7g.21816524A>TCA366948237DNAH11c.10390A>T (p.Thr3464Ser)
c.10411A>T (p.Thr3471Ser)
7g.21816525C>ACA366948240DNAH11c.10391C>A (p.Thr3464Lys)
c.10412C>A (p.Thr3471Lys)
7g.21816525C=CA1693666252DNAH11c.10391C= (p.Thr3464=)
c.10412C= (p.Thr3471=)
7g.21816525C>GCA366948241DNAH11c.10391C>G (p.Thr3464Arg)
c.10412C>G (p.Thr3471Arg)
7g.21816525C>TCA4182353DNAH11c.10391C>T (p.Thr3464Ile)
c.10412C>T (p.Thr3471Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816526A=CA1693666255DNAH11c.10392A= (p.Thr3464=)
c.10413A= (p.Thr3471=)
7g.21816526A>CCA453966587DNAH11c.10392A>C (p.Thr3464=)
c.10413A>C (p.Thr3471=)
7g.21816526A>GCA4182354DNAH11c.10392A>G (p.Thr3464=)
c.10413A>G (p.Thr3471=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816526A>TCA453966589DNAH11c.10392A>T (p.Thr3464=)
c.10413A>T (p.Thr3471=)
7g.21816527A=CA1693666258DNAH11c.10393A= (p.Ile3465=)
c.10414A= (p.Ile3472=)
7g.21816527A>CCA366948245DNAH11c.10393A>C (p.Ile3465Leu)
c.10414A>C (p.Ile3472Leu)
7g.21816527A>GCA155122122DNAH11c.10393A>G (p.Ile3465Val)
c.10414A>G (p.Ile3472Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.21816527A>TCA366948248DNAH11c.10393A>T (p.Ile3465Phe)
c.10414A>T (p.Ile3472Phe)
gnomAD v4
7g.21816528T>ACA366948250DNAH11c.10394T>A (p.Ile3465Asn)
c.10415T>A (p.Ile3472Asn)
7g.21816528T>CCA366948253DNAH11c.10394T>C (p.Ile3465Thr)
c.10415T>C (p.Ile3472Thr)
7g.21816528T>GCA366948254DNAH11c.10394T>G (p.Ile3465Ser)
c.10415T>G (p.Ile3472Ser)
7g.21816529T>ACA4182355DNAH11c.10395T>A (p.Ile3465=)
c.10416T>A (p.Ile3472=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
7g.21816529T>CCA453966591DNAH11c.10395T>C (p.Ile3465=)
c.10416T>C (p.Ile3472=)
7g.21816529T>GCA366948256DNAH11c.10395T>G (p.Ile3465Met)
c.10416T>G (p.Ile3472Met)
7g.21816529T=CA1693666262DNAH11c.10395T= (p.Ile3465=)
c.10416T= (p.Ile3472=)
7g.21816530G>ACA366948258DNAH11c.10396G>A (p.Ala3466Thr)
c.10417G>A (p.Ala3473Thr)
7g.21816530G>CCA366948259DNAH11c.10396G>C (p.Ala3466Pro)
c.10417G>C (p.Ala3473Pro)
7g.21816530G>TCA366948261DNAH11c.10396G>T (p.Ala3466Ser)
c.10417G>T (p.Ala3473Ser)
7g.21816531C>ACA366948268DNAH11c.10397C>A (p.Ala3466Asp)
c.10418C>A (p.Ala3473Asp)
7g.21816531C>GCA366948270DNAH11c.10397C>G (p.Ala3466Gly)
c.10418C>G (p.Ala3473Gly)
gnomAD v4
7g.21816531C>TCA366948265DNAH11c.10397C>T (p.Ala3466Val)
c.10418C>T (p.Ala3473Val)
7g.21816532C>ACA453966595DNAH11c.10398C>A (p.Ala3466=)
c.10419C>A (p.Ala3473=)
dbSNP gnomAD v4
7g.21816532C=CA1693666267DNAH11c.10398C= (p.Ala3466=)
c.10419C= (p.Ala3473=)
7g.21816532C>GCA453966596DNAH11c.10398C>G (p.Ala3466=)
c.10419C>G (p.Ala3473=)
gnomAD v4
7g.21816532C>TCA4182356DNAH11c.10398C>T (p.Ala3466=)
c.10419C>T (p.Ala3473=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816533G>ACA182902DNAH11c.10399G>A (p.Ala3467Thr)
c.10420G>A (p.Ala3474Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816533G>CCA366948276DNAH11c.10399G>C (p.Ala3467Pro)
c.10420G>C (p.Ala3474Pro)
ClinVar dbSNP gnomAD v4
7g.21816533G=CA1630834691DNAH11c.10399G= (p.Ala3467=)
c.10420G= (p.Ala3474=)
7g.21816533G>TCA366948278DNAH11c.10399G>T (p.Ala3467Ser)
c.10420G>T (p.Ala3474Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.21816534C>ACA366948285DNAH11c.10400C>A (p.Ala3467Asp)
c.10421C>A (p.Ala3474Asp)
7g.21816534C=CA1693666278DNAH11c.10400C= (p.Ala3467=)
c.10421C= (p.Ala3474=)
7g.21816534C>GCA366948284DNAH11c.10400C>G (p.Ala3467Gly)
c.10421C>G (p.Ala3474Gly)
7g.21816534C>TCA366948281DNAH11c.10400C>T (p.Ala3467Val)
c.10421C>T (p.Ala3474Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.21816535C>ACA453966597DNAH11c.10401C>A (p.Ala3467=)
c.10422C>A (p.Ala3474=)
ClinVar gnomAD v4
7g.21816535C>GCA453966598DNAH11c.10401C>G (p.Ala3467=)
c.10422C>G (p.Ala3474=)
7g.21816535C>TCA453966600DNAH11c.10401C>T (p.Ala3467=)
c.10422C>T (p.Ala3474=)
7g.21816536T>ACA366948288DNAH11c.10402T>A (p.Trp3468Arg)
c.10423T>A (p.Trp3475Arg)
7g.21816536T>CCA366948291DNAH11c.10402T>C (p.Trp3468Arg)
c.10423T>C (p.Trp3475Arg)
7g.21816536T>GCA366948294DNAH11c.10402T>G (p.Trp3468Gly)
c.10423T>G (p.Trp3475Gly)
7g.21816537G>ACA366948297DNAH11c.10403G>A (p.Trp3468Ter)
c.10424G>A (p.Trp3475Ter)
7g.21816537G>CCA366948300DNAH11c.10403G>C (p.Trp3468Ser)
c.10424G>C (p.Trp3475Ser)
7g.21816537G>TCA366948303DNAH11c.10403G>T (p.Trp3468Leu)
c.10424G>T (p.Trp3475Leu)
7g.21816538G>ACA366948312DNAH11c.10404G>A (p.Trp3468Ter)
c.10425G>A (p.Trp3475Ter)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.21816538G>CCA366948310DNAH11c.10404G>C (p.Trp3468Cys)
c.10425G>C (p.Trp3475Cys)
7g.21816538G=CA1693666280DNAH11c.10404G= (p.Trp3468=)
c.10425G= (p.Trp3475=)
7g.21816538G>TCA366948308DNAH11c.10404G>T (p.Trp3468Cys)
c.10425G>T (p.Trp3475Cys)
gnomAD v4
7g.21816539A>CCA366948315DNAH11c.10405A>C (p.Asn3469His)
c.10426A>C (p.Asn3476His)
7g.21816539A>GCA366948320DNAH11c.10405A>G (p.Asn3469Asp)
c.10426A>G (p.Asn3476Asp)
7g.21816539A>TCA366948318DNAH11c.10405A>T (p.Asn3469Tyr)
c.10426A>T (p.Asn3476Tyr)
7g.21816540A=CA1693666284DNAH11c.10406A= (p.Asn3469=)
c.10427A= (p.Asn3476=)
7g.21816540A>CCA366948323DNAH11c.10406A>C (p.Asn3469Thr)
c.10427A>C (p.Asn3476Thr)
7g.21816540A>GCA4182357DNAH11c.10406A>G (p.Asn3469Ser)
c.10427A>G (p.Asn3476Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816540A>TCA366948327DNAH11c.10406A>T (p.Asn3469Ile)
c.10427A>T (p.Asn3476Ile)
7g.21816541T>ACA366948331DNAH11c.10407T>A (p.Asn3469Lys)
c.10428T>A (p.Asn3476Lys)
7g.21816541T>CCA453966605DNAH11c.10407T>C (p.Asn3469=)
c.10428T>C (p.Asn3476=)
7g.21816541T>GCA366948334DNAH11c.10407T>G (p.Asn3469Lys)
c.10428T>G (p.Asn3476Lys)
7g.21816542A>CCA366948337DNAH11c.10408A>C (p.Asn3470His)
c.10429A>C (p.Asn3477His)
7g.21816542A>GCA366948339DNAH11c.10408A>G (p.Asn3470Asp)
c.10429A>G (p.Asn3477Asp)
7g.21816542A>TCA366948342DNAH11c.10408A>T (p.Asn3470Tyr)
c.10429A>T (p.Asn3477Tyr)
7g.21816543A>CCA366948344DNAH11c.10409A>C (p.Asn3470Thr)
c.10430A>C (p.Asn3477Thr)
7g.21816543A>GCA366948347DNAH11c.10409A>G (p.Asn3470Ser)
c.10430A>G (p.Asn3477Ser)
7g.21816543A>TCA366948349DNAH11c.10409A>T (p.Asn3470Ile)
c.10430A>T (p.Asn3477Ile)
7g.21816544C>ACA366948355DNAH11c.10410C>A (p.Asn3470Lys)
c.10431C>A (p.Asn3477Lys)
ClinVar gnomAD v4
7g.21816544C=CA1693666288DNAH11c.10410C= (p.Asn3470=)
c.10431C= (p.Asn3477=)
7g.21816544C>GCA4182358DNAH11c.10410C>G (p.Asn3470Lys)
c.10431C>G (p.Asn3477Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.21816544C>TCA155122144DNAH11c.10410C>T (p.Asn3470=)
c.10431C>T (p.Asn3477=)
ClinVar dbSNP gnomAD v3 gnomAD v4
7g.21816545G>ACA175745DNAH11c.10411G>A (p.Glu3471Lys)
c.10432G>A (p.Glu3478Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816545G>CCA366948362DNAH11c.10411G>C (p.Glu3471Gln)
c.10432G>C (p.Glu3478Gln)
7g.21816545G=CA1693666292DNAH11c.10411G= (p.Glu3471=)
c.10432G= (p.Glu3478=)
7g.21816545G>TCA366948361DNAH11c.10411G>T (p.Glu3471Ter)
c.10432G>T (p.Glu3478Ter)
7g.21816546A>CCA366948365DNAH11c.10412A>C (p.Glu3471Ala)
c.10433A>C (p.Glu3478Ala)
7g.21816546A>GCA366948369DNAH11c.10412A>G (p.Glu3471Gly)
c.10433A>G (p.Glu3478Gly)
7g.21816546A>TCA366948372DNAH11c.10412A>T (p.Glu3471Val)
c.10433A>T (p.Glu3478Val)
7g.21816547A=CA1693666297DNAH11c.10413A= (p.Glu3471=)
c.10434A= (p.Glu3478=)
7g.21816547A>CCA366948375DNAH11c.10413A>C (p.Glu3471Asp)
c.10434A>C (p.Glu3478Asp)
gnomAD v4
7g.21816547A>GCA155122146DNAH11c.10413A>G (p.Glu3471=)
c.10434A>G (p.Glu3478=)
dbSNP gnomAD v4
7g.21816547A>TCA366948378DNAH11c.10413A>T (p.Glu3471Asp)
c.10434A>T (p.Glu3478Asp)
7g.21816548G>ACA366948380DNAH11c.10414G>A (p.Gly3472Arg)
c.10435G>A (p.Gly3479Arg)
ClinVar dbSNP gnomAD v2
7g.21816548G>CCA366948382DNAH11c.10414G>C (p.Gly3472Arg)
c.10435G>C (p.Gly3479Arg)
7g.21816548G=CA1693666300DNAH11c.10414G= (p.Gly3472=)
c.10435G= (p.Gly3479=)
7g.21816548G>TCA366948385DNAH11c.10414G>T (p.Gly3472Ter)
c.10435G>T (p.Gly3479Ter)
7g.21816549G>ACA366948387DNAH11c.10415G>A (p.Gly3472Glu)
c.10436G>A (p.Gly3479Glu)
dbSNP gnomAD v2 gnomAD v4
7g.21816549G>CCA366948390DNAH11c.10415G>C (p.Gly3472Ala)
c.10436G>C (p.Gly3479Ala)
gnomAD v4
7g.21816549G=CA1693666302DNAH11c.10415G= (p.Gly3472=)
c.10436G= (p.Gly3479=)
7g.21816549G>TCA366948393DNAH11c.10415G>T (p.Gly3472Val)
c.10436G>T (p.Gly3479Val)
gnomAD v4
7g.21816550A>CCA453966614DNAH11c.10416A>C (p.Gly3472=)
c.10437A>C (p.Gly3479=)
7g.21816550A>GCA453966613DNAH11c.10416A>G (p.Gly3472=)
c.10437A>G (p.Gly3479=)
7g.21816550A>TCA453966611DNAH11c.10416A>T (p.Gly3472=)
c.10437A>T (p.Gly3479=)
7g.21816551C>ACA366948397DNAH11c.10417C>A (p.Leu3473Met)
c.10438C>A (p.Leu3480Met)
7g.21816551C>GCA366948401DNAH11c.10417C>G (p.Leu3473Val)
c.10438C>G (p.Leu3480Val)
7g.21816551C>TCA453966615DNAH11c.10417C>T (p.Leu3473=)
c.10438C>T (p.Leu3480=)
7g.21816552T>ACA366948405DNAH11c.10418T>A (p.Leu3473Gln)
c.10439T>A (p.Leu3480Gln)
7g.21816552T>CCA366948407DNAH11c.10418T>C (p.Leu3473Pro)
c.10439T>C (p.Leu3480Pro)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.21816552T>GCA366948410DNAH11c.10418T>G (p.Leu3473Arg)
c.10439T>G (p.Leu3480Arg)
7g.21816552T=CA1693666305DNAH11c.10418T= (p.Leu3473=)
c.10439T= (p.Leu3480=)
7g.21816553G>ACA453966618DNAH11c.10419G>A (p.Leu3473=)
c.10440G>A (p.Leu3480=)
7g.21816553G>CCA453966617DNAH11c.10419G>C (p.Leu3473=)
c.10440G>C (p.Leu3480=)
7g.21816553G=CA1693666315DNAH11c.10419G= (p.Leu3473=)
c.10440G= (p.Leu3480=)
7g.21816553G>TCA453966616DNAH11c.10419G>T (p.Leu3473=)
c.10440G>T (p.Leu3480=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
7g.21816554C>ACA366948413DNAH11c.10420C>A (p.Pro3474Thr)
c.10441C>A (p.Pro3481Thr)
gnomAD v4
7g.21816554C>GCA366948414DNAH11c.10420C>G (p.Pro3474Ala)
c.10441C>G (p.Pro3481Ala)
7g.21816554C>TCA366948416DNAH11c.10420C>T (p.Pro3474Ser)
c.10441C>T (p.Pro3481Ser)
gnomAD v4
7g.21816555C>ACA366948419DNAH11c.10421C>A (p.Pro3474His)
c.10442C>A (p.Pro3481His)
7g.21816555C=CA1693666318DNAH11c.10421C= (p.Pro3474=)
c.10442C= (p.Pro3481=)
7g.21816555C>GCA366948422DNAH11c.10421C>G (p.Pro3474Arg)
c.10442C>G (p.Pro3481Arg)
dbSNP
7g.21816555C>TCA366948426DNAH11c.10421C>T (p.Pro3474Leu)
c.10442C>T (p.Pro3481Leu)
dbSNP gnomAD v2
7g.21816556C>ACA453966621DNAH11c.10422C>A (p.Pro3474=)
c.10443C>A (p.Pro3481=)
7g.21816556C=CA1693666321DNAH11c.10422C= (p.Pro3474=)
c.10443C= (p.Pro3481=)
7g.21816556C>GCA453966622DNAH11c.10422C>G (p.Pro3474=)
c.10443C>G (p.Pro3481=)
7g.21816556C>TCA155122148DNAH11c.10422C>T (p.Pro3474=)
c.10443C>T (p.Pro3481=)
dbSNP gnomAD v4
7g.21816557A=CA1693666323DNAH11c.10423A= (p.Ser3475=)
c.10444A= (p.Ser3482=)
7g.21816557A>CCA4182359DNAH11c.10423A>C (p.Ser3475Arg)
c.10444A>C (p.Ser3482Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.21816557A>GCA366948432DNAH11c.10423A>G (p.Ser3475Gly)
c.10444A>G (p.Ser3482Gly)
gnomAD v4
7g.21816557A>TCA366948433DNAH11c.10423A>T (p.Ser3475Cys)
c.10444A>T (p.Ser3482Cys)
7g.21816558G>ACA366948442DNAH11c.10424G>A (p.Ser3475Asn)
c.10445G>A (p.Ser3482Asn)
7g.21816558G>CCA366948436DNAH11c.10424G>C (p.Ser3475Thr)
c.10445G>C (p.Ser3482Thr)
dbSNP gnomAD v2 gnomAD v4
7g.21816558G=CA1693666325DNAH11c.10424G= (p.Ser3475=)
c.10445G= (p.Ser3482=)
7g.21816558G>TCA366948439DNAH11c.10424G>T (p.Ser3475Ile)
c.10445G>T (p.Ser3482Ile)
7g.21816559T>ACA4182360DNAH11c.10425T>A (p.Ser3475Arg)
c.10446T>A (p.Ser3482Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.21816559T>CCA453966623DNAH11c.10425T>C (p.Ser3475=)
c.10446T>C (p.Ser3482=)
dbSNP
7g.21816559T>GCA366948445DNAH11c.10425T>G (p.Ser3475Arg)
c.10446T>G (p.Ser3482Arg)
7g.21816559T=CA1693666330DNAH11c.10425T= (p.Ser3475=)
c.10446T= (p.Ser3482=)
7g.21816560G>ACA366948449DNAH11c.10426G>A (p.Asp3476Asn)
c.10447G>A (p.Asp3483Asn)
7g.21816560G>CCA366948451DNAH11c.10426G>C (p.Asp3476His)
c.10447G>C (p.Asp3483His)
7g.21816560G>TCA366948453DNAH11c.10426G>T (p.Asp3476Tyr)
c.10447G>T (p.Asp3483Tyr)
7g.21816561A=CA1693666333DNAH11c.10427A= (p.Asp3476=)
c.10448A= (p.Asp3483=)
7g.21816561A>CCA366948456DNAH11c.10427A>C (p.Asp3476Ala)
c.10448A>C (p.Asp3483Ala)
7g.21816561A>GCA366948457DNAH11c.10427A>G (p.Asp3476Gly)
c.10448A>G (p.Asp3483Gly)
7g.21816561A>TCA4182361DNAH11c.10427A>T (p.Asp3476Val)
c.10448A>T (p.Asp3483Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816562C>ACA366948462DNAH11c.10428C>A (p.Asp3476Glu)
c.10449C>A (p.Asp3483Glu)
7g.21816562C>GCA366948465DNAH11c.10428C>G (p.Asp3476Glu)
c.10449C>G (p.Asp3483Glu)
7g.21816562C>TCA453966645DNAH11c.10428C>T (p.Asp3476=)
c.10449C>T (p.Asp3483=)
7g.21816563A>CCA453966646DNAH11c.10429A>C (p.Arg3477=)
c.10450A>C (p.Arg3484=)
gnomAD v4
7g.21816563A>GCA366948467DNAH11c.10429A>G (p.Arg3477Gly)
c.10450A>G (p.Arg3484Gly)
7g.21816563A>TCA366948470DNAH11c.10429A>T (p.Arg3477Ter)
c.10450A>T (p.Arg3484Ter)
7g.21816564G>ACA366948477DNAH11c.10430G>A (p.Arg3477Lys)
c.10451G>A (p.Arg3484Lys)
7g.21816564G>CCA366948476DNAH11c.10430G>C (p.Arg3477Thr)
c.10451G>C (p.Arg3484Thr)
7g.21816564G>TCA366948474DNAH11c.10430G>T (p.Arg3477Ile)
c.10451G>T (p.Arg3484Ile)
7g.21816565A=CA1693666339DNAH11c.10431A= (p.Arg3477=)
c.10452A= (p.Arg3484=)
7g.21816565A>CCA4182362DNAH11c.10431A>C (p.Arg3477Ser)
c.10452A>C (p.Arg3484Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816565A>GCA453966647DNAH11c.10431A>G (p.Arg3477=)
c.10452A>G (p.Arg3484=)
dbSNP
7g.21816565A>TCA366948479DNAH11c.10431A>T (p.Arg3477Ser)
c.10452A>T (p.Arg3484Ser)
7g.21816566A>CCA366948481DNAH11c.10432A>C (p.Met3478Leu)
c.10453A>C (p.Met3485Leu)
7g.21816566A>GCA366948482DNAH11c.10432A>G (p.Met3478Val)
c.10453A>G (p.Met3485Val)
gnomAD v4
7g.21816566A>TCA366948483DNAH11c.10432A>T (p.Met3478Leu)
c.10453A>T (p.Met3485Leu)
gnomAD v4
7g.21816567T>ACA366948484DNAH11c.10433T>A (p.Met3478Lys)
c.10454T>A (p.Met3485Lys)
7g.21816567T>CCA366948486DNAH11c.10433T>C (p.Met3478Thr)
c.10454T>C (p.Met3485Thr)
7g.21816567T>GCA366948488DNAH11c.10433T>G (p.Met3478Arg)
c.10454T>G (p.Met3485Arg)
7g.21816568G>ACA366948489DNAH11c.10434G>A (p.Met3478Ile)
c.10455G>A (p.Met3485Ile)
dbSNP gnomAD v2 gnomAD v4
7g.21816568G>CCA366948491DNAH11c.10434G>C (p.Met3478Ile)
c.10455G>C (p.Met3485Ile)
7g.21816568G=CA1693666341DNAH11c.10434G= (p.Met3478=)
c.10455G= (p.Met3485=)
7g.21816568G>TCA366948494DNAH11c.10434G>T (p.Met3478Ile)
c.10455G>T (p.Met3485Ile)
7g.21816569T>ACA366948498DNAH11c.10435T>A (p.Ser3479Thr)
c.10456T>A (p.Ser3486Thr)
7g.21816569T>CCA155122159DNAH11c.10435T>C (p.Ser3479Pro)
c.10456T>C (p.Ser3486Pro)
dbSNP gnomAD v2 gnomAD v4
7g.21816569T>GCA366948505DNAH11c.10435T>G (p.Ser3479Ala)
c.10456T>G (p.Ser3486Ala)
7g.21816569T=CA1693666343DNAH11c.10435T= (p.Ser3479=)
c.10456T= (p.Ser3486=)
7g.21816570C>ACA366948511DNAH11c.10436C>A (p.Ser3479Tyr)
c.10457C>A (p.Ser3486Tyr)
7g.21816570C>GCA366948510DNAH11c.10436C>G (p.Ser3479Cys)
c.10457C>G (p.Ser3486Cys)
gnomAD v4
7g.21816570C>TCA366948508DNAH11c.10436C>T (p.Ser3479Phe)
c.10457C>T (p.Ser3486Phe)
7g.21816571C>ACA453966650DNAH11c.10437C>A (p.Ser3479=)
c.10458C>A (p.Ser3486=)
7g.21816571C=CA1693666345DNAH11c.10437C= (p.Ser3479=)
c.10458C= (p.Ser3486=)
7g.21816571C>GCA453966649DNAH11c.10437C>G (p.Ser3479=)
c.10458C>G (p.Ser3486=)
7g.21816571C>TCA453966648DNAH11c.10437C>T (p.Ser3479=)
c.10458C>T (p.Ser3486=)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.21816572A>CCA366948517DNAH11c.10438A>C (p.Thr3480Pro)
c.10459A>C (p.Thr3487Pro)
7g.21816572A>GCA366948521DNAH11c.10438A>G (p.Thr3480Ala)
c.10459A>G (p.Thr3487Ala)
7g.21816572A>TCA366948523DNAH11c.10438A>T (p.Thr3480Ser)
c.10459A>T (p.Thr3487Ser)
7g.21816573C>ACA366948526DNAH11c.10439C>A (p.Thr3480Asn)
c.10460C>A (p.Thr3487Asn)
gnomAD v4
7g.21816573C>GCA366948528DNAH11c.10439C>G (p.Thr3480Ser)
c.10460C>G (p.Thr3487Ser)
7g.21816573C>TCA366948531DNAH11c.10439C>T (p.Thr3480Ile)
c.10460C>T (p.Thr3487Ile)
gnomAD v4
7g.21816574C>ACA453966651DNAH11c.10440C>A (p.Thr3480=)
c.10461C>A (p.Thr3487=)
ClinVar gnomAD v4
7g.21816574C=CA1693666349DNAH11c.10440C= (p.Thr3480=)
c.10461C= (p.Thr3487=)
7g.21816574C>GCA155122168DNAH11c.10440C>G (p.Thr3480=)
c.10461C>G (p.Thr3487=)
ClinVar dbSNP gnomAD v4
7g.21816574C>TCA4182363DNAH11c.10440C>T (p.Thr3480=)
c.10461C>T (p.Thr3487=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816575G>ACA175747DNAH11c.10441G>A (p.Glu3481Lys)
c.10462G>A (p.Glu3488Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
7g.21816575G>CCA366948538DNAH11c.10441G>C (p.Glu3481Gln)
c.10462G>C (p.Glu3488Gln)
7g.21816575G=CA1693666356DNAH11c.10441G= (p.Glu3481=)
c.10462G= (p.Glu3488=)
7g.21816575G>TCA366948540DNAH11c.10441G>T (p.Glu3481Ter)
c.10462G>T (p.Glu3488Ter)
dbSNP gnomAD v2 gnomAD v4
7g.21816576A>CCA366948541DNAH11c.10442A>C (p.Glu3481Ala)
c.10463A>C (p.Glu3488Ala)
7g.21816576A>GCA366948543DNAH11c.10442A>G (p.Glu3481Gly)
c.10463A>G (p.Glu3488Gly)
7g.21816576A>TCA366948545DNAH11c.10442A>T (p.Glu3481Val)
c.10463A>T (p.Glu3488Val)
7g.21816579delCA645563171DNAH11c.10445del (p.Asn3482MetfsTer5)
c.10466del (p.Asn3489MetfsTer5)
COSMIC COSMIC
7g.21816577A>CCA366948548DNAH11c.10443A>C (p.Glu3481Asp)
c.10464A>C (p.Glu3488Asp)
7g.21816577A>GCA453966652DNAH11c.10443A>G (p.Glu3481=)
c.10464A>G (p.Glu3488=)
gnomAD v4
7g.21816577A>TCA366948551DNAH11c.10443A>T (p.Glu3481Asp)
c.10464A>T (p.Glu3488Asp)
7g.21816578A=CA1693666365DNAH11c.10444A= (p.Asn3482=)
c.10465A= (p.Asn3489=)
7g.21816578A>CCA366948557DNAH11c.10444A>C (p.Asn3482His)
c.10465A>C (p.Asn3489His)
dbSNP gnomAD v3 gnomAD v4
7g.21816578A>GCA366948559DNAH11c.10444A>G (p.Asn3482Asp)
c.10465A>G (p.Asn3489Asp)
7g.21816578A>TCA366948554DNAH11c.10444A>T (p.Asn3482Tyr)
c.10465A>T (p.Asn3489Tyr)
7g.21816579A>CCA366948562DNAH11c.10445A>C (p.Asn3482Thr)
c.10466A>C (p.Asn3489Thr)
7g.21816579A>GCA366948566DNAH11c.10445A>G (p.Asn3482Ser)
c.10466A>G (p.Asn3489Ser)
7g.21816579A>TCA366948567DNAH11c.10445A>T (p.Asn3482Ile)
c.10466A>T (p.Asn3489Ile)
gnomAD v4
7g.21816580T>ACA366948569DNAH11c.10446T>A (p.Asn3482Lys)
c.10467T>A (p.Asn3489Lys)
dbSNP
7g.21816580T>CCA453966653DNAH11c.10446T>C (p.Asn3482=)
c.10467T>C (p.Asn3489=)
7g.21816580T>GCA366948572DNAH11c.10446T>G (p.Asn3482Lys)
c.10467T>G (p.Asn3489Lys)
7g.21816580T=CA1693666366DNAH11c.10446T= (p.Asn3482=)
c.10467T= (p.Asn3489=)
7g.21816581G>ACA366948576DNAH11c.10447G>A (p.Ala3483Thr)
c.10468G>A (p.Ala3490Thr)
7g.21816581G>CCA366948579DNAH11c.10447G>C (p.Ala3483Pro)
c.10468G>C (p.Ala3490Pro)
7g.21816581G>TCA366948581DNAH11c.10447G>T (p.Ala3483Ser)
c.10468G>T (p.Ala3490Ser)
7g.21816582C>ACA366948584DNAH11c.10448C>A (p.Ala3483Asp)
c.10469C>A (p.Ala3490Asp)
7g.21816582C>GCA366948587DNAH11c.10448C>G (p.Ala3483Gly)
c.10469C>G (p.Ala3490Gly)
7g.21816582C>TCA366948589DNAH11c.10448C>T (p.Ala3483Val)
c.10469C>T (p.Ala3490Val)
gnomAD v4 COSMIC COSMIC
7g.21816583C>ACA453966655DNAH11c.10449C>A (p.Ala3483=)
c.10470C>A (p.Ala3490=)
gnomAD v3 gnomAD v4 COSMIC COSMIC
7g.21816583C=CA1693666371DNAH11c.10449C= (p.Ala3483=)
c.10470C= (p.Ala3490=)
7g.21816583C>GCA453966654DNAH11c.10449C>G (p.Ala3483=)
c.10470C>G (p.Ala3490=)
gnomAD v4
7g.21816583C>TCA4182364DNAH11c.10449C>T (p.Ala3483=)
c.10470C>T (p.Ala3490=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816584G>ACA4182365DNAH11c.10450G>A (p.Ala3484Thr)
c.10471G>A (p.Ala3491Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816584G>CCA366948596DNAH11c.10450G>C (p.Ala3484Pro)
c.10471G>C (p.Ala3491Pro)
7g.21816584G=CA1693666376DNAH11c.10450G= (p.Ala3484=)
c.10471G= (p.Ala3491=)
7g.21816584G>TCA366948593DNAH11c.10450G>T (p.Ala3484Ser)
c.10471G>T (p.Ala3491Ser)
7g.21816585C>ACA366948597DNAH11c.10451C>A (p.Ala3484Asp)
c.10472C>A (p.Ala3491Asp)
7g.21816585C>GCA366948598DNAH11c.10451C>G (p.Ala3484Gly)
c.10472C>G (p.Ala3491Gly)
7g.21816585C>TCA366948599DNAH11c.10451C>T (p.Ala3484Val)
c.10472C>T (p.Ala3491Val)
gnomAD v4
7g.21816586T>ACA453966656DNAH11c.10452T>A (p.Ala3484=)
c.10473T>A (p.Ala3491=)
7g.21816586T>CCA453966657DNAH11c.10452T>C (p.Ala3484=)
c.10473T>C (p.Ala3491=)
7g.21816586T>GCA453966658DNAH11c.10452T>G (p.Ala3484=)
c.10473T>G (p.Ala3491=)
7g.21816587A=CA1693666378DNAH11c.10453A= (p.Ile3485=)
c.10474A= (p.Ile3492=)
7g.21816587A>CCA366948600DNAH11c.10453A>C (p.Ile3485Leu)
c.10474A>C (p.Ile3492Leu)
7g.21816587A>GCA366948602DNAH11c.10453A>G (p.Ile3485Val)
c.10474A>G (p.Ile3492Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.21816587A>TCA366948604DNAH11c.10453A>T (p.Ile3485Phe)
c.10474A>T (p.Ile3492Phe)
7g.21816588T>ACA366948606DNAH11c.10454T>A (p.Ile3485Asn)
c.10475T>A (p.Ile3492Asn)
7g.21816588T>CCA4182366DNAH11c.10454T>C (p.Ile3485Thr)
c.10475T>C (p.Ile3492Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.21816588T>GCA366948608DNAH11c.10454T>G (p.Ile3485Ser)
c.10475T>G (p.Ile3492Ser)
7g.21816588T=CA1693666381DNAH11c.10454T= (p.Ile3485=)
c.10475T= (p.Ile3492=)
7g.21816589C>ACA453966659DNAH11c.10455C>A (p.Ile3485=)
c.10476C>A (p.Ile3492=)
7g.21816589C=CA1693666383DNAH11c.10455C= (p.Ile3485=)
c.10476C= (p.Ile3492=)
7g.21816589C>GCA366948613DNAH11c.10455C>G (p.Ile3485Met)
c.10476C>G (p.Ile3492Met)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.21816589C>TCA4182367DNAH11c.10455C>T (p.Ile3485=)
c.10476C>T (p.Ile3492=)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.21816590C>ACA366948616DNAH11c.10456C>A (p.Leu3486Ile)
c.10477C>A (p.Leu3493Ile)
7g.21816590C=CA1693666389DNAH11c.10456C= (p.Leu3486=)
c.10477C= (p.Leu3493=)
7g.21816590C>GCA366948622DNAH11c.10456C>G (p.Leu3486Val)
c.10477C>G (p.Leu3493Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.21816590C>TCA453966660DNAH11c.10456C>T (p.Leu3486=)
c.10477C>T (p.Leu3493=)
ClinVar
7g.21816591T>ACA366948626DNAH11c.10457T>A (p.Leu3486Gln)
c.10478T>A (p.Leu3493Gln)
7g.21816591T>CCA155122186DNAH11c.10457T>C (p.Leu3486Pro)
c.10478T>C (p.Leu3493Pro)
dbSNP
7g.21816591T>GCA366948629DNAH11c.10457T>G (p.Leu3486Arg)
c.10478T>G (p.Leu3493Arg)
7g.21816591T=CA1693666394DNAH11c.10457T= (p.Leu3486=)
c.10478T= (p.Leu3493=)
7g.21816592A>CCA453966661DNAH11c.10458A>C (p.Leu3486=)
c.10479A>C (p.Leu3493=)
7g.21816592A>GCA453966662DNAH11c.10458A>G (p.Leu3486=)
c.10479A>G (p.Leu3493=)
ClinVar
7g.21816592A>TCA453966663DNAH11c.10458A>T (p.Leu3486=)
c.10479A>T (p.Leu3493=)
7g.21816592_21816595delCA2681989635DNAH11c.10458_10461del (p.His3488ValfsTer7)
c.10479_10482del (p.His3495ValfsTer7)
gnomAD v4
7g.21816593A>CCA366948633DNAH11c.10459A>C (p.Thr3487Pro)
c.10480A>C (p.Thr3494Pro)
7g.21816593A>GCA366948637DNAH11c.10459A>G (p.Thr3487Ala)
c.10480A>G (p.Thr3494Ala)
7g.21816593A>TCA366948640DNAH11c.10459A>T (p.Thr3487Ser)
c.10480A>T (p.Thr3494Ser)
7g.21816594C>ACA366948643DNAH11c.10460C>A (p.Thr3487Lys)
c.10481C>A (p.Thr3494Lys)
7g.21816594C>GCA366948645DNAH11c.10460C>G (p.Thr3487Arg)
c.10481C>G (p.Thr3494Arg)
7g.21816594C>TCA366948647DNAH11c.10460C>T (p.Thr3487Ile)
c.10481C>T (p.Thr3494Ile)
7g.21816595A=CA1693666398DNAH11c.10461A= (p.Thr3487=)
c.10482A= (p.Thr3494=)
7g.21816595A>CCA453966664DNAH11c.10461A>C (p.Thr3487=)
c.10482A>C (p.Thr3494=)
7g.21816595A>GCA453966665DNAH11c.10461A>G (p.Thr3487=)
c.10482A>G (p.Thr3494=)
7g.21816595A>TCA155122189DNAH11c.10461A>T (p.Thr3487=)
c.10482A>T (p.Thr3494=)
dbSNP gnomAD v4
7g.21816596C>ACA366948656DNAH11c.10462C>A (p.His3488Asn)
c.10483C>A (p.His3495Asn)
7g.21816596C>GCA366948650DNAH11c.10462C>G (p.His3488Asp)
c.10483C>G (p.His3495Asp)
gnomAD v4
7g.21816596C>TCA366948653DNAH11c.10462C>T (p.His3488Tyr)
c.10483C>T (p.His3495Tyr)
7g.21816597A=CA1693666400DNAH11c.10463A= (p.His3488=)
c.10484A= (p.His3495=)
7g.21816597A>CCA366948658DNAH11c.10463A>C (p.His3488Pro)
c.10484A>C (p.His3495Pro)
7g.21816597A>GCA4182368DNAH11c.10463A>G (p.His3488Arg)
c.10484A>G (p.His3495Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816597A>TCA366948662DNAH11c.10463A>T (p.His3488Leu)
c.10484A>T (p.His3495Leu)
gnomAD v4
7g.21816598C>ACA366948665DNAH11c.10464C>A (p.His3488Gln)
c.10485C>A (p.His3495Gln)
7g.21816598C=CA1693666405DNAH11c.10464C= (p.His3488=)
c.10485C= (p.His3495=)
7g.21816598C>GCA4182369DNAH11c.10464C>G (p.His3488Gln)
c.10485C>G (p.His3495Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816598C>TCA453966666DNAH11c.10464C>T (p.His3488=)
c.10485C>T (p.His3495=)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.21816599T>ACA366948673DNAH11c.10465T>A (p.Cys3489Ser)
c.10486T>A (p.Cys3496Ser)
7g.21816599T>CCA366948669DNAH11c.10465T>C (p.Cys3489Arg)
c.10486T>C (p.Cys3496Arg)
7g.21816599T>GCA366948671DNAH11c.10465T>G (p.Cys3489Gly)
c.10486T>G (p.Cys3496Gly)
7g.21816600G>ACA4182370DNAH11c.10466G>A (p.Cys3489Tyr)
c.10487G>A (p.Cys3496Tyr)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.21816600G>CCA366948676DNAH11c.10466G>C (p.Cys3489Ser)
c.10487G>C (p.Cys3496Ser)
COSMIC COSMIC
7g.21816600G=CA1693666410DNAH11c.10466G= (p.Cys3489=)
c.10487G= (p.Cys3496=)
7g.21816600G>TCA366948679DNAH11c.10466G>T (p.Cys3489Phe)
c.10487G>T (p.Cys3496Phe)
7g.21816601T>ACA366948682DNAH11c.10467T>A (p.Cys3489Ter)
c.10488T>A (p.Cys3496Ter)
7g.21816601T>CCA453966667DNAH11c.10467T>C (p.Cys3489=)
c.10488T>C (p.Cys3496=)
7g.21816601T>GCA366948685DNAH11c.10467T>G (p.Cys3489Trp)
c.10488T>G (p.Cys3496Trp)
7g.21816602G>ACA366948688DNAH11c.10468G>A (p.Glu3490Lys)
c.10489G>A (p.Glu3497Lys)
COSMIC COSMIC
7g.21816602G>CCA366948692DNAH11c.10468G>C (p.Glu3490Gln)
c.10489G>C (p.Glu3497Gln)
7g.21816602G>TCA366948694DNAH11c.10468G>T (p.Glu3490Ter)
c.10489G>T (p.Glu3497Ter)
7g.21816603A>CCA366948699DNAH11c.10469A>C (p.Glu3490Ala)
c.10490A>C (p.Glu3497Ala)
7g.21816603A>GCA366948705DNAH11c.10469A>G (p.Glu3490Gly)
c.10490A>G (p.Glu3497Gly)
gnomAD v4
7g.21816603A>TCA366948707DNAH11c.10469A>T (p.Glu3490Val)
c.10490A>T (p.Glu3497Val)
7g.21816604G>ACA453966668DNAH11c.10470G>A (p.Glu3490=)
c.10491G>A (p.Glu3497=)
dbSNP gnomAD v4
7g.21816604G>CCA366948709DNAH11c.10470G>C (p.Glu3490Asp)
c.10491G>C (p.Glu3497Asp)
7g.21816604G=CA1693666413DNAH11c.10470G= (p.Glu3490=)
c.10491G= (p.Glu3497=)
7g.21816604G>TCA366948712DNAH11c.10470G>T (p.Glu3490Asp)
c.10491G>T (p.Glu3497Asp)
7g.21816605C>ACA366948716DNAH11c.10471C>A (p.Arg3491Ser)
c.10492C>A (p.Arg3498Ser)
7g.21816605C=CA1693666417DNAH11c.10471C= (p.Arg3491=)
c.10492C= (p.Arg3498=)
7g.21816605C>GCA366948720DNAH11c.10471C>G (p.Arg3491Gly)
c.10492C>G (p.Arg3498Gly)
dbSNP gnomAD v2 gnomAD v4
7g.21816605C>TCA366948718DNAH11c.10471C>T (p.Arg3491Cys)
c.10492C>T (p.Arg3498Cys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
7g.21816606G>ACA246938DNAH11c.10472G>A (p.Arg3491His)
c.10493G>A (p.Arg3498His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21816606G>CCA366948724DNAH11c.10472G>C (p.Arg3491Pro)
c.10493G>C (p.Arg3498Pro)
dbSNP
7g.21816606G=CA1693666423DNAH11c.10472G= (p.Arg3491=)
c.10493G= (p.Arg3498=)
7g.21816606G>TCA366948727DNAH11c.10472G>T (p.Arg3491Leu)
c.10493G>T (p.Arg3498Leu)

Number of alleles fetched