Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49457933delCA450608622MMUTc.514del (p.Ile172PhefsTer8)
ClinVar dbSNP gnomAD v4 COSMIC
6g.49457933T>ACA364404573MMUTc.511A>T (p.Lys171Ter)
ClinVar
6g.49457933T>CCA364404574MMUTc.511A>G (p.Lys171Glu)
dbSNP gnomAD v2 gnomAD v4
6g.49457933T>GCA364404575MMUTc.511A>C (p.Lys171Gln)
6g.49457933T=CA1627395343MMUTc.511A= (p.Lys171=)
6g.49457934G>ACA450608624MMUTc.510C>T (p.Thr170=)
gnomAD v4
6g.49457934G>CCA3847099MMUTc.510C>G (p.Thr170=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49457934G=CA1627395347MMUTc.510C= (p.Thr170=)
6g.49457934G>TCA450608625MMUTc.510C>A (p.Thr170=)
6g.49457935G>ACA364404576MMUTc.509C>T (p.Thr170Ile)
ClinVar
6g.49457935G>CCA364404578MMUTc.509C>G (p.Thr170Ser)
ClinVar dbSNP gnomAD v4
6g.49457935G>TCA364404577MMUTc.509C>A (p.Thr170Asn)
gnomAD v4
6g.49457936T>ACA364404579MMUTc.508A>T (p.Thr170Ser)
gnomAD v4
6g.49457936T>CCA364404580MMUTc.508A>G (p.Thr170Ala)
6g.49457936T>GCA364404581MMUTc.508A>C (p.Thr170Pro)
6g.49457937A=CA1627395349MMUTc.507T= (p.Asp169=)
6g.49457937A>CCA364404582MMUTc.507T>G (p.Asp169Glu)
6g.49457937A>GCA450608626MMUTc.507T>C (p.Asp169=)
ClinVar dbSNP
6g.49457937A>TCA364404583MMUTc.507T>A (p.Asp169Glu)
6g.49457938T>ACA364404584MMUTc.506A>T (p.Asp169Val)
6g.49457938T>CCA364404585MMUTc.506A>G (p.Asp169Gly)
6g.49457938T>GCA364404586MMUTc.506A>C (p.Asp169Ala)
6g.49457939C>ACA364404587MMUTc.505G>T (p.Asp169Tyr)
6g.49457939C>GCA364404588MMUTc.505G>C (p.Asp169His)
6g.49457939C>TCA364404589MMUTc.505G>A (p.Asp169Asn)
6g.49457940T>ACA364404590MMUTc.504A>T (p.Glu168Asp)
6g.49457940T>CCA450608627MMUTc.504A>G (p.Glu168=)
6g.49457940T>GCA364404591MMUTc.504A>C (p.Glu168Asp)
6g.49457941delCA2695206688MMUTc.504del (p.Asp169IlefsTer11)
6g.49457941T>ACA364404592MMUTc.503A>T (p.Glu168Val)
6g.49457941T>CCA364404593MMUTc.503A>G (p.Glu168Gly)
dbSNP gnomAD v2 gnomAD v4
6g.49457941T>GCA364404594MMUTc.503A>C (p.Glu168Ala)
6g.49457941T=CA1627395352MMUTc.503A= (p.Glu168=)
6g.49457942C>ACA364404595MMUTc.502G>T (p.Glu168Ter)
6g.49457942C>GCA364404596MMUTc.502G>C (p.Glu168Gln)
6g.49457942C>TCA364404597MMUTc.502G>A (p.Glu168Lys)
6g.49457943C>ACA450608628MMUTc.501G>T (p.Val167=)
6g.49457943C>GCA450608629MMUTc.501G>C (p.Val167=)
6g.49457943C>TCA450608630MMUTc.501G>A (p.Val167=)
6g.49457944A=CA1627395356MMUTc.500T= (p.Val167=)
6g.49457944A>CCA364404598MMUTc.500T>G (p.Val167Gly)
6g.49457944A>GCA364404599MMUTc.500T>C (p.Val167Ala)
dbSNP gnomAD v2 gnomAD v4
6g.49457944A>TCA364404600MMUTc.500T>A (p.Val167Glu)
6g.49457945C>ACA364404601MMUTc.499G>T (p.Val167Leu)
6g.49457945C=CA1627395361MMUTc.499G= (p.Val167=)
6g.49457945C>GCA364404602MMUTc.499G>C (p.Val167Leu)
6g.49457945C>TCA3847100MMUTc.499G>A (p.Val167Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.49457946A>CCA450608633MMUTc.498T>G (p.Thr166=)
6g.49457946A>GCA450608632MMUTc.498T>C (p.Thr166=)
ClinVar gnomAD v4
6g.49457946A>TCA450608631MMUTc.498T>A (p.Thr166=)
6g.49457947G>ACA364404605MMUTc.497C>T (p.Thr166Ile)
6g.49457947G>CCA364404604MMUTc.497C>G (p.Thr166Ser)
6g.49457947G>TCA364404603MMUTc.497C>A (p.Thr166Asn)
6g.49457948T>ACA364404606MMUTc.496A>T (p.Thr166Ser)
6g.49457948T>CCA364404607MMUTc.496A>G (p.Thr166Ala)
dbSNP gnomAD v3 gnomAD v4
6g.49457948T>GCA364404608MMUTc.496A>C (p.Thr166Pro)
6g.49457948T=CA1627395367MMUTc.496A= (p.Thr166=)
6g.49457949G>ACA450608634MMUTc.495C>T (p.Asp165=)
6g.49457949G>CCA364404609MMUTc.495C>G (p.Asp165Glu)
6g.49457949G>TCA364404610MMUTc.495C>A (p.Asp165Glu)
6g.49457950T>ACA364404611MMUTc.494A>T (p.Asp165Val)
6g.49457950T>CCA138799926MMUTc.494A>G (p.Asp165Gly)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
6g.49457950T>GCA364404612MMUTc.494A>C (p.Asp165Ala)
6g.49457950T=CA1627395373MMUTc.494A= (p.Asp165=)
6g.49457951C>ACA364404613MMUTc.493G>T (p.Asp165Tyr)
6g.49457951C>GCA364404614MMUTc.493G>C (p.Asp165His)
6g.49457951C>TCA364404615MMUTc.493G>A (p.Asp165Asn)
6g.49457952A>CCA364404616MMUTc.492T>G (p.Ile164Met)
6g.49457952A>GCA450608636MMUTc.492T>C (p.Ile164=)
6g.49457952A>TCA450608635MMUTc.492T>A (p.Ile164=)
6g.49457953A=CA1627395377MMUTc.491T= (p.Ile164=)
6g.49457953A>CCA364404618MMUTc.491T>G (p.Ile164Ser)
6g.49457953A>GCA364404617MMUTc.491T>C (p.Ile164Thr)
6g.49457953A>TCA3847101MMUTc.491T>A (p.Ile164Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49457954T>ACA364404619MMUTc.490A>T (p.Ile164Phe)
6g.49457954T>CCA364404621MMUTc.490A>G (p.Ile164Val)
dbSNP gnomAD v4
6g.49457954T>GCA364404620MMUTc.490A>C (p.Ile164Leu)
6g.49457954T=CA1627395381MMUTc.490A= (p.Ile164=)
6g.49457955A>CCA450608637MMUTc.489T>G (p.Ala163=)
6g.49457955A>GCA450608638MMUTc.489T>C (p.Ala163=)
ClinVar
6g.49457955A>TCA450608639MMUTc.489T>A (p.Ala163=)
6g.49457956G>ACA364404622MMUTc.488C>T (p.Ala163Val)
dbSNP gnomAD v3 gnomAD v4
6g.49457956G>CCA364404623MMUTc.488C>G (p.Ala163Gly)
gnomAD v4
6g.49457956G=CA1627395383MMUTc.488C= (p.Ala163=)
6g.49457956G>TCA364404624MMUTc.488C>A (p.Ala163Asp)
6g.49457957C>ACA364404625MMUTc.487G>T (p.Ala163Ser)
6g.49457957C>GCA364404626MMUTc.487G>C (p.Ala163Pro)
6g.49457957C>TCA364404627MMUTc.487G>A (p.Ala163Thr)
6g.49457958A>CCA450608640MMUTc.486T>G (p.Val162=)
6g.49457958A>GCA450608642MMUTc.486T>C (p.Val162=)
6g.49457958A>TCA450608641MMUTc.486T>A (p.Val162=)
6g.49457959A=CA1627395386MMUTc.485T= (p.Val162=)
6g.49457959A>CCA364404628MMUTc.485T>G (p.Val162Gly)
dbSNP gnomAD v4
6g.49457959A>GCA364404629MMUTc.485T>C (p.Val162Ala)
COSMIC
6g.49457959A>TCA364404630MMUTc.485T>A (p.Val162Asp)
6g.49457960C>ACA364404631MMUTc.484G>T (p.Val162Phe)
6g.49457960C>GCA364404632MMUTc.484G>C (p.Val162Leu)
6g.49457960C>TCA364404633MMUTc.484G>A (p.Val162Ile)
6g.49457961T>ACA450608643MMUTc.483A>T (p.Gly161=)
6g.49457961T>CCA3847102MMUTc.483A>G (p.Gly161=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49457961T>GCA450608644MMUTc.483A>C (p.Gly161=)
ClinVar gnomAD v4
6g.49457961T=CA1627395388MMUTc.483A= (p.Gly161=)
6g.49457962C>ACA364404636MMUTc.482G>T (p.Gly161Val)
6g.49457962C>GCA364404634MMUTc.482G>C (p.Gly161Ala)
6g.49457962C>TCA364404635MMUTc.482G>A (p.Gly161Glu)
6g.49457963C>ACA364404637MMUTc.481G>T (p.Gly161Ter)
6g.49457963C>GCA364404638MMUTc.481G>C (p.Gly161Arg)
6g.49457963C>TCA364404639MMUTc.481G>A (p.Gly161Arg)
ClinVar dbSNP gnomAD v4
6g.49457964A>CCA450608645MMUTc.480T>G (p.Ala160=)
6g.49457964A>GCA450608646MMUTc.480T>C (p.Ala160=)
6g.49457964A>TCA450608647MMUTc.480T>A (p.Ala160=)
6g.49457965G>ACA364404640MMUTc.479C>T (p.Ala160Val)
gnomAD v4
6g.49457965G>CCA364404641MMUTc.479C>G (p.Ala160Gly)
6g.49457965G>TCA364404642MMUTc.479C>A (p.Ala160Asp)
6g.49457966C>ACA364404643MMUTc.478G>T (p.Ala160Ser)
dbSNP
6g.49457966C>GCA364404644MMUTc.478G>C (p.Ala160Pro)
6g.49457966C>TCA364404645MMUTc.478G>A (p.Ala160Thr)
6g.49457967C>ACA364404646MMUTc.477G>T (p.Met159Ile)
6g.49457967C>GCA364404647MMUTc.477G>C (p.Met159Ile)
6g.49457967C>TCA364404648MMUTc.477G>A (p.Met159Ile)
6g.49457968A>CCA364404649MMUTc.476T>G (p.Met159Arg)
6g.49457968A>GCA364404651MMUTc.476T>C (p.Met159Thr)
6g.49457968A>TCA364404650MMUTc.476T>A (p.Met159Lys)
6g.49457969T>ACA364404652MMUTc.475A>T (p.Met159Leu)
6g.49457969T>CCA364404653MMUTc.475A>G (p.Met159Val)
6g.49457969T>GCA364404654MMUTc.475A>C (p.Met159Leu)
6g.49457970T>ACA450608648MMUTc.474A>T (p.Gly158=)
6g.49457970T>CCA450608649MMUTc.474A>G (p.Gly158=)
6g.49457970T>GCA450608650MMUTc.474A>C (p.Gly158=)
6g.49457971C>ACA364404655MMUTc.473G>T (p.Gly158Val)
6g.49457971C>GCA364404656MMUTc.473G>C (p.Gly158Ala)
6g.49457971C>TCA364404657MMUTc.473G>A (p.Gly158Glu)
6g.49457972C>ACA364404658MMUTc.472G>T (p.Gly158Ter)
6g.49457972C>GCA364404659MMUTc.472G>C (p.Gly158Arg)
gnomAD v4
6g.49457972C>TCA364404660MMUTc.472G>A (p.Gly158Arg)
gnomAD v4
6g.49457973A>CCA450608651MMUTc.471T>G (p.Val157=)
6g.49457973A>GCA450608652MMUTc.471T>C (p.Val157=)
6g.49457973A>TCA450608653MMUTc.471T>A (p.Val157=)
6g.49457974A>CCA364404661MMUTc.470T>G (p.Val157Gly)
6g.49457974A>GCA364404662MMUTc.470T>C (p.Val157Ala)
6g.49457974A>TCA364404663MMUTc.470T>A (p.Val157Asp)
6g.49457975C>ACA364404666MMUTc.469G>T (p.Val157Phe)
6g.49457975C>GCA364404664MMUTc.469G>C (p.Val157Leu)
6g.49457975C>TCA364404665MMUTc.469G>A (p.Val157Ile)
6g.49457976A=CA1627395391MMUTc.468T= (p.Asp156=)
6g.49457976A>CCA364404667MMUTc.468T>G (p.Asp156Glu)
6g.49457976A>GCA450608655MMUTc.468T>C (p.Asp156=)
gnomAD v4
6g.49457976A>TCA364404668MMUTc.468T>A (p.Asp156Glu)
dbSNP
6g.49457977T>ACA3847103MMUTc.467A>T (p.Asp156Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.49457977T>CCA364404669MMUTc.467A>G (p.Asp156Gly)
dbSNP gnomAD v3 gnomAD v4
6g.49457977T>GCA364404670MMUTc.467A>C (p.Asp156Ala)
6g.49457977T=CA1627395396MMUTc.467A= (p.Asp156=)
6g.49457978C>ACA364404671MMUTc.466G>T (p.Asp156Tyr)
6g.49457978C>GCA364404672MMUTc.466G>C (p.Asp156His)
6g.49457978C>TCA364404673MMUTc.466G>A (p.Asp156Asn)
ClinVar gnomAD v4
6g.49457981_49457983delCA2695206689MMUTc.464_466del (p.Gly155del)
6g.49457979A>CCA450608658MMUTc.465T>G (p.Gly155=)
6g.49457979A>GCA450608659MMUTc.465T>C (p.Gly155=)
6g.49457979A>TCA450608660MMUTc.465T>A (p.Gly155=)
6g.49457980C>ACA364404674MMUTc.464G>T (p.Gly155Val)
gnomAD v4
6g.49457980C=CA1627395403MMUTc.464G= (p.Gly155=)
6g.49457980C>GCA364404675MMUTc.464G>C (p.Gly155Ala)
6g.49457980C>TCA3847104MMUTc.464G>A (p.Gly155Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49457981C>ACA364404677MMUTc.463G>T (p.Gly155Cys)
gnomAD v4
6g.49457981C>GCA364404678MMUTc.463G>C (p.Gly155Arg)
6g.49457981C>TCA364404676MMUTc.463G>A (p.Gly155Ser)
6g.49457982A>CCA450608661MMUTc.462T>G (p.Arg154=)
6g.49457982A>GCA450608662MMUTc.462T>C (p.Arg154=)
6g.49457982A>TCA450608663MMUTc.462T>A (p.Arg154=)
gnomAD v4
6g.49457983C>ACA364404680MMUTc.461G>T (p.Arg154Leu)
gnomAD v4
6g.49457983C=CA1627395411MMUTc.461G= (p.Arg154=)
6g.49457983C>GCA364404679MMUTc.461G>C (p.Arg154Pro)
6g.49457983C>TCA3847105MMUTc.461G>A (p.Arg154His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49457984G>ACA364404681MMUTc.460C>T (p.Arg154Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49457984G>CCA364404682MMUTc.460C>G (p.Arg154Gly)
6g.49457984G=CA1627395419MMUTc.460C= (p.Arg154=)
6g.49457984G>TCA364404683MMUTc.460C>A (p.Arg154Ser)
gnomAD v4
6g.49457985A>CCA450608665MMUTc.459T>G (p.Val153=)
6g.49457985A>GCA450608666MMUTc.459T>C (p.Val153=)
6g.49457985A>TCA450608667MMUTc.459T>A (p.Val153=)
6g.49457986delCA2695206690MMUTc.459del (p.Arg154ValfsTer26)
6g.49457986A>CCA364404684MMUTc.458T>G (p.Val153Gly)
6g.49457986A>GCA364404685MMUTc.458T>C (p.Val153Ala)
6g.49457986A>TCA364404686MMUTc.458T>A (p.Val153Asp)
6g.49457987C>ACA364404687MMUTc.457G>T (p.Val153Phe)
6g.49457987C=CA1627395424MMUTc.457G= (p.Val153=)
6g.49457987C>GCA364404688MMUTc.457G>C (p.Val153Leu)
6g.49457987C>TCA364404689MMUTc.457G>A (p.Val153Ile)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49457988T>ACA450608670MMUTc.456A>T (p.Arg152=)
6g.49457988T>CCA450608669MMUTc.456A>G (p.Arg152=)
6g.49457988T>GCA450608668MMUTc.456A>C (p.Arg152=)
6g.49457989C>ACA364404691MMUTc.455G>T (p.Arg152Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.49457989C=CA1627395431MMUTc.455G= (p.Arg152=)
6g.49457989C>GCA364404690MMUTc.455G>C (p.Arg152Pro)
6g.49457989C>TCA3847106MMUTc.455G>A (p.Arg152Gln)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49457990G>ACA3847107MMUTc.454C>T (p.Arg152Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49457990G>CCA364404692MMUTc.454C>G (p.Arg152Gly)
6g.49457990G=CA1627395439MMUTc.454C= (p.Arg152=)
6g.49457990G>TCA450608671MMUTc.454C>A (p.Arg152=)
6g.49457991A>CCA450608672MMUTc.453T>G (p.Pro151=)
6g.49457991A>GCA450608673MMUTc.453T>C (p.Pro151=)
6g.49457991A>TCA450608674MMUTc.453T>A (p.Pro151=)
6g.49457992G>ACA364404693MMUTc.452C>T (p.Pro151Leu)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.49457992G>CCA364404694MMUTc.452C>G (p.Pro151Arg)
gnomAD v4
6g.49457992G=CA1627395441MMUTc.452C= (p.Pro151=)
6g.49457992G>TCA364404695MMUTc.452C>A (p.Pro151His)
6g.49457993G>ACA364404696MMUTc.451C>T (p.Pro151Ser)
gnomAD v4 COSMIC
6g.49457993G>CCA364404697MMUTc.451C>G (p.Pro151Ala)
6g.49457993G>TCA364404698MMUTc.451C>A (p.Pro151Thr)
6g.49457994G>ACA450608675MMUTc.450C>T (p.Asn150=)
ClinVar dbSNP gnomAD v4
6g.49457994G>CCA364404699MMUTc.450C>G (p.Asn150Lys)
6g.49457994G=CA1627395443MMUTc.450C= (p.Asn150=)
6g.49457994G>TCA364404700MMUTc.450C>A (p.Asn150Lys)
6g.49457995T>ACA364404701MMUTc.449A>T (p.Asn150Ile)
6g.49457995T>CCA138799965MMUTc.449A>G (p.Asn150Ser)
dbSNP gnomAD v3 gnomAD v4
6g.49457995T>GCA364404702MMUTc.449A>C (p.Asn150Thr)
6g.49457995T=CA1627395447MMUTc.449A= (p.Asn150=)
6g.49457996T>ACA364404704MMUTc.448A>T (p.Asn150Tyr)
6g.49457996T>CCA364404705MMUTc.448A>G (p.Asn150Asp)
6g.49457996T>GCA364404703MMUTc.448A>C (p.Asn150His)
6g.49457997G>ACA450608676MMUTc.447C>T (p.Asp149=)
gnomAD v4
6g.49457997G>CCA364404706MMUTc.447C>G (p.Asp149Glu)
6g.49457997G=CA1627395449MMUTc.447C= (p.Asp149=)
6g.49457997G>TCA364404707MMUTc.447C>A (p.Asp149Glu)
ClinVar
6g.49457998T>ACA364404708MMUTc.446A>T (p.Asp149Val)
ClinVar dbSNP
6g.49457998T>CCA364404709MMUTc.446A>G (p.Asp149Gly)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.49457998T>GCA364404710MMUTc.446A>C (p.Asp149Ala)
6g.49457998T=CA1627395460MMUTc.446A= (p.Asp149=)
6g.49457998dupCA1139659603MMUTc.446dup (p.Asp149GlufsTer8)
ClinVar dbSNP
6g.49457999C>ACA364404711MMUTc.445G>T (p.Asp149Tyr)
6g.49457999C>GCA364404712MMUTc.445G>C (p.Asp149His)
6g.49457999C>TCA364404713MMUTc.445G>A (p.Asp149Asn)
6g.49458000T>ACA450608677MMUTc.444A>T (p.Ser148=)
6g.49458000T>CCA450608678MMUTc.444A>G (p.Ser148=)
6g.49458000T>GCA450608679MMUTc.444A>C (p.Ser148=)
dbSNP gnomAD v2 gnomAD v4
6g.49458000T=CA1627395465MMUTc.444A= (p.Ser148=)
6g.49458001G>ACA364404714MMUTc.443C>T (p.Ser148Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.49458001G>CCA364404715MMUTc.443C>G (p.Ser148Ter)
dbSNP gnomAD v2 gnomAD v4
6g.49458001G=CA1627395469MMUTc.443C= (p.Ser148=)
6g.49458001G>TCA364404716MMUTc.443C>A (p.Ser148Ter)
6g.49458002A>CCA364404717MMUTc.442T>G (p.Ser148Ala)
6g.49458002A>GCA364404718MMUTc.442T>C (p.Ser148Pro)
6g.49458002A>TCA364404719MMUTc.442T>A (p.Ser148Thr)
6g.49458003A>CCA364404721MMUTc.441T>G (p.Asp147Glu)
6g.49458003A>GCA450608680MMUTc.441T>C (p.Asp147=)
gnomAD v4
6g.49458003A>TCA364404720MMUTc.441T>A (p.Asp147Glu)
6g.49458004T>ACA364404722MMUTc.440A>T (p.Asp147Val)
6g.49458004T>CCA364404723MMUTc.440A>G (p.Asp147Gly)
6g.49458004T>GCA364404724MMUTc.440A>C (p.Asp147Ala)
6g.49458005C>ACA364404725MMUTc.439G>T (p.Asp147Tyr)
gnomAD v4
6g.49458005C>GCA364404726MMUTc.439G>C (p.Asp147His)
6g.49458005C>TCA364404727MMUTc.439G>A (p.Asp147Asn)
6g.49458006delCA2582341703MMUTc.438del (p.Tyr146Ter)
ClinVar
6g.49458006A=CA1627395472MMUTc.438T= (p.Tyr146=)
6g.49458006A>CCA364404729MMUTc.438T>G (p.Tyr146Ter)
6g.49458006A>GCA3847108MMUTc.438T>C (p.Tyr146=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458006A>TCA364404728MMUTc.438T>A (p.Tyr146Ter)
ClinVar dbSNP
6g.49458007T>ACA364404730MMUTc.437A>T (p.Tyr146Phe)
6g.49458007T>CCA3847109MMUTc.437A>G (p.Tyr146Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458007T>GCA364404731MMUTc.437A>C (p.Tyr146Ser)
6g.49458007T=CA1627395476MMUTc.437A= (p.Tyr146=)
6g.49458008A>CCA364404732MMUTc.436T>G (p.Tyr146Asp)
6g.49458008A>GCA364404733MMUTc.436T>C (p.Tyr146His)
6g.49458008A>TCA364404734MMUTc.436T>A (p.Tyr146Asn)
6g.49458008dupCA2695206691MMUTc.436dup (p.Tyr146LeufsTer2)
6g.49458009G>ACA450608681MMUTc.435C>T (p.Gly145=)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
6g.49458009G>CCA450608682MMUTc.435C>G (p.Gly145=)
6g.49458009G=CA1627395481MMUTc.435C= (p.Gly145=)
6g.49458009G>TCA450608683MMUTc.435C>A (p.Gly145=)
6g.49458010C>ACA364404736MMUTc.434G>T (p.Gly145Val)
dbSNP gnomAD v2 gnomAD v4
6g.49458010C=CA1627395482MMUTc.434G= (p.Gly145=)
6g.49458010C>GCA364404737MMUTc.434G>C (p.Gly145Ala)
6g.49458010C>TCA364404735MMUTc.434G>A (p.Gly145Asp)
gnomAD v4 COSMIC
6g.49458011C>ACA364404738MMUTc.433G>T (p.Gly145Cys)
dbSNP gnomAD v2
6g.49458011C=CA1627395484MMUTc.433G= (p.Gly145=)
6g.49458011C>GCA364404740MMUTc.433G>C (p.Gly145Arg)
6g.49458011C>TCA364404739MMUTc.433G>A (p.Gly145Ser)
dbSNP gnomAD v4
6g.49458012A>CCA450608684MMUTc.432T>G (p.Arg144=)
6g.49458012A>GCA450608685MMUTc.432T>C (p.Arg144=)
6g.49458012A>TCA450608686MMUTc.432T>A (p.Arg144=)
6g.49458013C>ACA364404741MMUTc.431G>T (p.Arg144Leu)
6g.49458013C=CA1627395489MMUTc.431G= (p.Arg144=)
6g.49458013C>GCA364404742MMUTc.431G>C (p.Arg144Pro)
6g.49458013C>TCA3847110MMUTc.431G>A (p.Arg144His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458014G>ACA364404743MMUTc.430C>T (p.Arg144Cys)
ClinVar gnomAD v4
6g.49458014G>CCA364404745MMUTc.430C>G (p.Arg144Gly)
gnomAD v4
6g.49458014G>TCA364404744MMUTc.430C>A (p.Arg144Ser)
6g.49458015A>CCA364404746MMUTc.429T>G (p.His143Gln)
6g.49458015A>GCA450608687MMUTc.429T>C (p.His143=)
6g.49458015A>TCA364404747MMUTc.429T>A (p.His143Gln)
6g.49458016T>ACA364404748MMUTc.428A>T (p.His143Leu)
6g.49458016T>CCA364404749MMUTc.428A>G (p.His143Arg)
gnomAD v4
6g.49458016T>GCA364404750MMUTc.428A>C (p.His143Pro)
6g.49458017_49458020delCA2578675210MMUTc.425_428del (p.Thr142IlefsTer?)
6g.49458017G>ACA364404751MMUTc.427C>T (p.His143Tyr)
gnomAD v4
6g.49458017G>CCA364404752MMUTc.427C>G (p.His143Asp)
6g.49458017G>TCA364404753MMUTc.427C>A (p.His143Asn)
6g.49458018delCA2573140887MMUTc.426del (p.His143IlefsTer?)
ClinVar dbSNP gnomAD v4
6g.49458018T>ACA450608688MMUTc.426A>T (p.Thr142=)
6g.49458018T>CCA450608689MMUTc.426A>G (p.Thr142=)
gnomAD v4
6g.49458018T>GCA450608690MMUTc.426A>C (p.Thr142=)
6g.49458019G>ACA364404754MMUTc.425C>T (p.Thr142Ile)
6g.49458019G>CCA364404755MMUTc.425C>G (p.Thr142Arg)
6g.49458019G>TCA364404756MMUTc.425C>A (p.Thr142Lys)
gnomAD v4
6g.49458020T>ACA364404759MMUTc.424A>T (p.Thr142Ser)
6g.49458020T>CCA364404758MMUTc.424A>G (p.Thr142Ala)
ClinVar
6g.49458020T>GCA364404757MMUTc.424A>C (p.Thr142Pro)
6g.49458021C>ACA450608691MMUTc.423G>T (p.Ala141=)
ClinVar dbSNP
6g.49458021C=CA1627395492MMUTc.423G= (p.Ala141=)
6g.49458021C>GCA450608692MMUTc.423G>C (p.Ala141=)
6g.49458021C>TCA3847111MMUTc.423G>A (p.Ala141=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458021_49458022insAAACA2578675211MMUTc.422_423insTTT (p.Ala141_Thr142insLeu)
6g.49458022G>ACA3847112MMUTc.422C>T (p.Ala141Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.49458022G>CCA364404760MMUTc.422C>G (p.Ala141Gly)
6g.49458022G=CA1627395501MMUTc.422C= (p.Ala141=)
6g.49458022G>TCA3847113MMUTc.422C>A (p.Ala141Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458022_49458023delinsGCCA1627395509MMUTc.421_422delinsGC (p.Ala141=)
6g.49458023C>ACA364404761MMUTc.421G>T (p.Ala141Ser)
6g.49458023C=CA1627395521MMUTc.421G= (p.Ala141=)
6g.49458023C>GCA364404762MMUTc.421G>C (p.Ala141Pro)
6g.49458023C>TCA364404763MMUTc.421G>A (p.Ala141Thr)
ClinVar dbSNP
6g.49458024delCA1139659605MMUTc.421del (p.Ala141ArgfsTer?)
ClinVar dbSNP
6g.49458024C>ACA450608693MMUTc.420G>T (p.Leu140=)
6g.49458024C=CA1627395532MMUTc.420G= (p.Leu140=)
6g.49458024C>GCA450608694MMUTc.420G>C (p.Leu140=)
6g.49458024C>TCA3847114MMUTc.420G>A (p.Leu140=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49458025A>CCA364404764MMUTc.419T>G (p.Leu140Arg)
6g.49458025A>GCA364404765MMUTc.419T>C (p.Leu140Pro)
6g.49458025A>TCA364404766MMUTc.419T>A (p.Leu140Gln)
6g.49458026G>ACA450608695MMUTc.418C>T (p.Leu140=)
gnomAD v4
6g.49458026G>CCA364404767MMUTc.418C>G (p.Leu140Val)
6g.49458026G>TCA364404768MMUTc.418C>A (p.Leu140Met)
gnomAD v4
6g.49458027A>CCA364404770MMUTc.417T>G (p.Asp139Glu)
6g.49458027A>GCA450608696MMUTc.417T>C (p.Asp139=)
gnomAD v4
6g.49458027A>TCA364404769MMUTc.417T>A (p.Asp139Glu)
6g.49458028T>ACA364404771MMUTc.416A>T (p.Asp139Val)
6g.49458028T>CCA364404772MMUTc.416A>G (p.Asp139Gly)
6g.49458028T>GCA364404773MMUTc.416A>C (p.Asp139Ala)
6g.49458029C>ACA364404774MMUTc.415G>T (p.Asp139Tyr)
6g.49458029C=CA1627395536MMUTc.415G= (p.Asp139=)
6g.49458029C>GCA364404775MMUTc.415G>C (p.Asp139His)
6g.49458029C>TCA10575882MMUTc.415G>A (p.Asp139Asn)
ClinVar dbSNP
6g.49458030A>CCA364404777MMUTc.414T>G (p.Phe138Leu)
6g.49458030A>GCA450608697MMUTc.414T>C (p.Phe138=)
ClinVar dbSNP gnomAD v4
6g.49458030A>TCA364404776MMUTc.414T>A (p.Phe138Leu)
6g.49458030_49458048delinsGTGGCTTTATATATTCA2580075487MMUTc.396_414delinsAATATATAAAGCCAC (p.Gly133IlefsTer?)
ClinVar
6g.49458031A>CCA364404778MMUTc.413T>G (p.Phe138Cys)
6g.49458031A>GCA364404779MMUTc.413T>C (p.Phe138Ser)
6g.49458031A>TCA364404780MMUTc.413T>A (p.Phe138Tyr)
gnomAD v4
6g.49458032A>CCA364404781MMUTc.412T>G (p.Phe138Val)
6g.49458032A>GCA364404782MMUTc.412T>C (p.Phe138Leu)
6g.49458032A>TCA364404783MMUTc.412T>A (p.Phe138Ile)
6g.49458033G>ACA450608698MMUTc.411C>T (p.Ala137=)
6g.49458033G>CCA450608699MMUTc.411C>G (p.Ala137=)
6g.49458033G>TCA450608700MMUTc.411C>A (p.Ala137=)

Number of alleles fetched