Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.17793736T>ACA398546200RAI1c.788T>A (p.Val263Asp)
c.722T>A (p.Val241Asp)
dbSNP
17g.17793736T>CCA398546201RAI1c.788T>C (p.Val263Ala)
c.722T>C (p.Val241Ala)
17g.17793736T>GCA398546202RAI1c.788T>G (p.Val263Gly)
c.722T>G (p.Val241Gly)
dbSNP
17g.17793736T=CA2250666812RAI1c.788T= (p.Val263=)
c.722T= (p.Val241=)
17g.17793737C>ACA288367269RAI1c.789C>A (p.Val263=)
c.723C>A (p.Val241=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.17793737C=CA2250666816RAI1c.789C= (p.Val263=)
c.723C= (p.Val241=)
17g.17793737C>GCA498422788RAI1c.789C>G (p.Val263=)
c.723C>G (p.Val241=)
17g.17793737C>TCA498422789RAI1c.789C>T (p.Val263=)
c.723C>T (p.Val241=)
dbSNP gnomAD v3 gnomAD v4
17g.17793738C>ACA398546205RAI1c.790C>A (p.Gln264Lys)
c.724C>A (p.Gln242Lys)
17g.17793738C=CA2250666828RAI1c.790C= (p.Gln264=)
c.724C= (p.Gln242=)
17g.17793738C>GCA398546203RAI1c.790C>G (p.Gln264Glu)
c.724C>G (p.Gln242Glu)
17g.17793738C>TCA398546204RAI1c.790C>T (p.Gln264Ter)
c.724C>T (p.Gln242Ter)
dbSNP
17g.17793739A=CA2250666831RAI1c.791A= (p.Gln264=)
c.725A= (p.Gln242=)
17g.17793739A>CCA398546206RAI1c.791A>C (p.Gln264Pro)
c.725A>C (p.Gln242Pro)
dbSNP gnomAD v2 gnomAD v4
17g.17793739A>GCA398546207RAI1c.791A>G (p.Gln264Arg)
c.725A>G (p.Gln242Arg)
gnomAD v4
17g.17793739A>TCA398546208RAI1c.791A>T (p.Gln264Leu)
c.725A>T (p.Gln242Leu)
17g.17793740G>ACA498422793RAI1c.792G>A (p.Gln264=)
c.726G>A (p.Gln242=)
17g.17793740G>CCA398546209RAI1c.792G>C (p.Gln264His)
c.726G>C (p.Gln242His)
17g.17793740G>TCA398546210RAI1c.792G>T (p.Gln264His)
c.726G>T (p.Gln242His)
17g.17793741A>CCA398546211RAI1c.793A>C (p.Asn265His)
c.727A>C (p.Asn243His)
17g.17793741A>GCA398546213RAI1c.793A>G (p.Asn265Asp)
c.727A>G (p.Asn243Asp)
17g.17793741A>TCA398546212RAI1c.793A>T (p.Asn265Tyr)
c.727A>T (p.Asn243Tyr)
17g.17793742A>CCA398546214RAI1c.794A>C (p.Asn265Thr)
c.728A>C (p.Asn243Thr)
17g.17793742A>GCA398546215RAI1c.794A>G (p.Asn265Ser)
c.728A>G (p.Asn243Ser)
gnomAD v4
17g.17793742A>TCA398546216RAI1c.794A>T (p.Asn265Ile)
c.728A>T (p.Asn243Ile)
17g.17793743T>ACA398546217RAI1c.795T>A (p.Asn265Lys)
c.729T>A (p.Asn243Lys)
17g.17793743T>CCA498422797RAI1c.795T>C (p.Asn265=)
c.729T>C (p.Asn243=)
17g.17793743T>GCA398546218RAI1c.795T>G (p.Asn265Lys)
c.729T>G (p.Asn243Lys)
17g.17793744C>ACA398546220RAI1c.796C>A (p.Leu266Ile)
c.730C>A (p.Leu244Ile)
17g.17793744C=CA2250666837RAI1c.796C= (p.Leu266=)
c.730C= (p.Leu244=)
17g.17793744C>GCA398546219RAI1c.796C>G (p.Leu266Val)
c.730C>G (p.Leu244Val)
17g.17793744C>TCA8418196RAI1c.796C>T (p.Leu266Phe)
c.730C>T (p.Leu244Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793745T>ACA398546221RAI1c.797T>A (p.Leu266His)
c.731T>A (p.Leu244His)
17g.17793745T>CCA398546222RAI1c.797T>C (p.Leu266Pro)
c.731T>C (p.Leu244Pro)
ClinVar gnomAD v4
17g.17793745T>GCA398546223RAI1c.797T>G (p.Leu266Arg)
c.731T>G (p.Leu244Arg)
17g.17793746T>ACA498422801RAI1c.798T>A (p.Leu266=)
c.732T>A (p.Leu244=)
17g.17793746T>CCA498422802RAI1c.798T>C (p.Leu266=)
c.732T>C (p.Leu244=)
17g.17793746T>GCA498422803RAI1c.798T>G (p.Leu266=)
c.732T>G (p.Leu244=)
17g.17793747C>ACA398546224RAI1c.799C>A (p.His267Asn)
c.733C>A (p.His245Asn)
17g.17793747C>GCA398546225RAI1c.799C>G (p.His267Asp)
c.733C>G (p.His245Asp)
17g.17793747C>TCA398546226RAI1c.799C>T (p.His267Tyr)
c.733C>T (p.His245Tyr)
17g.17793748A=CA2250666841RAI1c.800A= (p.His267=)
c.734A= (p.His245=)
17g.17793748A>CCA398546227RAI1c.800A>C (p.His267Pro)
c.734A>C (p.His245Pro)
gnomAD v4
17g.17793748A>GCA8418197RAI1c.800A>G (p.His267Arg)
c.734A>G (p.His245Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793748A>TCA398546228RAI1c.800A>T (p.His267Leu)
c.734A>T (p.His245Leu)
gnomAD v4
17g.17793749T>ACA398546229RAI1c.801T>A (p.His267Gln)
c.735T>A (p.His245Gln)
gnomAD v4
17g.17793749T>CCA8418198RAI1c.801T>C (p.His267=)
c.735T>C (p.His245=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793749T>GCA398546230RAI1c.801T>G (p.His267Gln)
c.735T>G (p.His245Gln)
17g.17793749T=CA2250666846RAI1c.801T= (p.His267=)
c.735T= (p.His245=)
17g.17793750G>ACA398546231RAI1c.802G>A (p.Ala268Thr)
c.736G>A (p.Ala246Thr)
17g.17793750G>CCA398546232RAI1c.802G>C (p.Ala268Pro)
c.736G>C (p.Ala246Pro)
17g.17793750G>TCA398546233RAI1c.802G>T (p.Ala268Ser)
c.736G>T (p.Ala246Ser)
17g.17793751C>ACA398546234RAI1c.803C>A (p.Ala268Asp)
c.737C>A (p.Ala246Asp)
17g.17793751C>GCA398546235RAI1c.803C>G (p.Ala268Gly)
c.737C>G (p.Ala246Gly)
17g.17793751C>TCA398546236RAI1c.803C>T (p.Ala268Val)
c.737C>T (p.Ala246Val)
gnomAD v4
17g.17793752C>ACA8418199RAI1c.804C>A (p.Ala268=)
c.738C>A (p.Ala246=)
dbSNP ExAC gnomAD v4
17g.17793752C=CA2250666850RAI1c.804C= (p.Ala268=)
c.738C= (p.Ala246=)
17g.17793752C>GCA498422808RAI1c.804C>G (p.Ala268=)
c.738C>G (p.Ala246=)
17g.17793752C>TCA498422807RAI1c.804C>T (p.Ala268=)
c.738C>T (p.Ala246=)
17g.17793753T>ACA398546239RAI1c.805T>A (p.Tyr269Asn)
c.739T>A (p.Tyr247Asn)
17g.17793753T>CCA398546237RAI1c.805T>C (p.Tyr269His)
c.739T>C (p.Tyr247His)
dbSNP gnomAD v3 gnomAD v4
17g.17793753T>GCA398546238RAI1c.805T>G (p.Tyr269Asp)
c.739T>G (p.Tyr247Asp)
17g.17793753T=CA2250666854RAI1c.805T= (p.Tyr269=)
c.739T= (p.Tyr247=)
17g.17793754A>CCA398546240RAI1c.806A>C (p.Tyr269Ser)
c.740A>C (p.Tyr247Ser)
17g.17793754A>GCA398546242RAI1c.806A>G (p.Tyr269Cys)
c.740A>G (p.Tyr247Cys)
17g.17793754A>TCA398546241RAI1c.806A>T (p.Tyr269Phe)
c.740A>T (p.Tyr247Phe)
17g.17793755C>ACA398546243RAI1c.807C>A (p.Tyr269Ter)
c.741C>A (p.Tyr247Ter)
17g.17793755C>GCA398546244RAI1c.807C>G (p.Tyr269Ter)
c.741C>G (p.Tyr247Ter)
17g.17793755C>TCA498422813RAI1c.807C>T (p.Tyr269=)
c.741C>T (p.Tyr247=)
gnomAD v4
17g.17793756C>ACA8418200RAI1c.808C>A (p.Gln270Lys)
c.742C>A (p.Gln248Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.17793756C=CA2250666859RAI1c.808C= (p.Gln270=)
c.742C= (p.Gln248=)
17g.17793756C>GCA398546245RAI1c.808C>G (p.Gln270Glu)
c.742C>G (p.Gln248Glu)
17g.17793756C>TCA398546246RAI1c.808C>T (p.Gln270Ter)
c.742C>T (p.Gln248Ter)
17g.17793757A=CA2250666877RAI1c.809A= (p.Gln270=)
c.743A= (p.Gln248=)
17g.17793757A>CCA8418201RAI1c.809A>C (p.Gln270Pro)
c.743A>C (p.Gln248Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.17793757A>GCA398546247RAI1c.809A>G (p.Gln270Arg)
c.743A>G (p.Gln248Arg)
17g.17793757A>TCA398546248RAI1c.809A>T (p.Gln270Leu)
c.743A>T (p.Gln248Leu)
17g.17793758G>ACA498422931RAI1c.810G>A (p.Gln270=)
c.744G>A (p.Gln248=)
dbSNP gnomAD v4
17g.17793758G>CCA398546249RAI1c.810G>C (p.Gln270His)
c.744G>C (p.Gln248His)
ClinVar
17g.17793758G=CA2250666884RAI1c.810G= (p.Gln270=)
c.744G= (p.Gln248=)
17g.17793758G>TCA398546250RAI1c.810G>T (p.Gln270His)
c.744G>T (p.Gln248His)
17g.17793759T>ACA398546253RAI1c.811T>A (p.Ser271Thr)
c.745T>A (p.Ser249Thr)
17g.17793759T>CCA398546252RAI1c.811T>C (p.Ser271Pro)
c.745T>C (p.Ser249Pro)
17g.17793759T>GCA398546251RAI1c.811T>G (p.Ser271Ala)
c.745T>G (p.Ser249Ala)
17g.17793760C>ACA398546254RAI1c.812C>A (p.Ser271Ter)
c.746C>A (p.Ser249Ter)
17g.17793760C=CA2250666887RAI1c.812C= (p.Ser271=)
c.746C= (p.Ser249=)
17g.17793760C>GCA398546255RAI1c.812C>G (p.Ser271Trp)
c.746C>G (p.Ser249Trp)
17g.17793760C>TCA398546256RAI1c.812C>T (p.Ser271Leu)
c.746C>T (p.Ser249Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.17793761G>ACA8418202RAI1c.813G>A (p.Ser271=)
c.747G>A (p.Ser249=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793761G>CCA8418203RAI1c.813G>C (p.Ser271=)
c.747G>C (p.Ser249=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793761G=CA2250666892RAI1c.813G= (p.Ser271=)
c.747G= (p.Ser249=)
17g.17793761G>TCA498422937RAI1c.813G>T (p.Ser271=)
c.747G>T (p.Ser249=)
17g.17793762G>ACA398546257RAI1c.814G>A (p.Gly272Ser)
c.748G>A (p.Gly250Ser)
ClinVar dbSNP
17g.17793762G>CCA398546258RAI1c.814G>C (p.Gly272Arg)
c.748G>C (p.Gly250Arg)
17g.17793762G=CA2250666896RAI1c.814G= (p.Gly272=)
c.748G= (p.Gly250=)
17g.17793762G>TCA8418204RAI1c.814G>T (p.Gly272Cys)
c.748G>T (p.Gly250Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793762_17793763insCACA2636388224RAI1c.814_815insCA (p.Gly272AlafsTer?)
c.748_749insCA (p.Gly250AlafsTer?)
gnomAD v4
17g.17793763G>ACA398546259RAI1c.815G>A (p.Gly272Asp)
c.749G>A (p.Gly250Asp)
17g.17793763G>CCA398546260RAI1c.815G>C (p.Gly272Ala)
c.749G>C (p.Gly250Ala)
17g.17793763G>TCA398546261RAI1c.815G>T (p.Gly272Val)
c.749G>T (p.Gly250Val)
17g.17793764C>ACA498422941RAI1c.816C>A (p.Gly272=)
c.750C>A (p.Gly250=)
17g.17793764C=CA2250666904RAI1c.816C= (p.Gly272=)
c.750C= (p.Gly250=)
17g.17793764C>GCA498422942RAI1c.816C>G (p.Gly272=)
c.750C>G (p.Gly250=)
17g.17793764C>TCA288367279RAI1c.816C>T (p.Gly272=)
c.750C>T (p.Gly250=)
dbSNP gnomAD v3 gnomAD v4
17g.17793764_17793765insTATGAGCTACCA2636388225RAI1c.816_817insTATGAGCTAC (p.Arg273TyrfsTer8)
c.750_751insTATGAGCTAC (p.Arg251TyrfsTer8)
gnomAD v4
17g.17793765C>ACA398546263RAI1c.817C>A (p.Arg273Ser)
c.751C>A (p.Arg251Ser)
17g.17793765C=CA2250666907RAI1c.817C= (p.Arg273=)
c.751C= (p.Arg251=)
17g.17793765C>GCA398546262RAI1c.817C>G (p.Arg273Gly)
c.751C>G (p.Arg251Gly)
17g.17793765C>TCA8418205RAI1c.817C>T (p.Arg273Cys)
c.751C>T (p.Arg251Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793766G>ACA8418206RAI1c.818G>A (p.Arg273His)
c.752G>A (p.Arg251His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.17793766G>CCA398546264RAI1c.818G>C (p.Arg273Pro)
c.752G>C (p.Arg251Pro)
17g.17793766G=CA2250666909RAI1c.818G= (p.Arg273=)
c.752G= (p.Arg251=)
17g.17793766G>TCA398546265RAI1c.818G>T (p.Arg273Leu)
c.752G>T (p.Arg251Leu)
17g.17793767C>ACA498422949RAI1c.819C>A (p.Arg273=)
c.753C>A (p.Arg251=)
17g.17793767C>GCA498422944RAI1c.819C>G (p.Arg273=)
c.753C>G (p.Arg251=)
17g.17793767C>TCA498422946RAI1c.819C>T (p.Arg273=)
c.753C>T (p.Arg251=)
gnomAD v4
17g.17793768C>ACA398546266RAI1c.820C>A (p.Leu274Ile)
c.754C>A (p.Leu252Ile)
17g.17793768C>GCA398546267RAI1c.820C>G (p.Leu274Val)
c.754C>G (p.Leu252Val)
17g.17793768C>TCA398546268RAI1c.820C>T (p.Leu274Phe)
c.754C>T (p.Leu252Phe)
gnomAD v4
17g.17793769T>ACA398546269RAI1c.821T>A (p.Leu274His)
c.755T>A (p.Leu252His)
17g.17793769T>CCA398546270RAI1c.821T>C (p.Leu274Pro)
c.755T>C (p.Leu252Pro)
17g.17793769T>GCA398546271RAI1c.821T>G (p.Leu274Arg)
c.755T>G (p.Leu252Arg)
17g.17793770C>ACA498422951RAI1c.822C>A (p.Leu274=)
c.756C>A (p.Leu252=)
17g.17793770C>GCA498422952RAI1c.822C>G (p.Leu274=)
c.756C>G (p.Leu252=)
17g.17793770C>TCA498422953RAI1c.822C>T (p.Leu274=)
c.756C>T (p.Leu252=)
gnomAD v4
17g.17793771A>CCA398546272RAI1c.823A>C (p.Ser275Arg)
c.757A>C (p.Ser253Arg)
17g.17793771A>GCA398546273RAI1c.823A>G (p.Ser275Gly)
c.757A>G (p.Ser253Gly)
17g.17793771A>TCA398546274RAI1c.823A>T (p.Ser275Cys)
c.757A>T (p.Ser253Cys)
17g.17793772G>ACA398546277RAI1c.824G>A (p.Ser275Asn)
c.758G>A (p.Ser253Asn)
17g.17793772G>CCA398546276RAI1c.824G>C (p.Ser275Thr)
c.758G>C (p.Ser253Thr)
17g.17793772G>TCA398546275RAI1c.824G>T (p.Ser275Ile)
c.758G>T (p.Ser253Ile)
17g.17793773C>ACA398546278RAI1c.825C>A (p.Ser275Arg)
c.759C>A (p.Ser253Arg)
17g.17793773C>GCA398546279RAI1c.825C>G (p.Ser275Arg)
c.759C>G (p.Ser253Arg)
COSMIC
17g.17793773C>TCA498422957RAI1c.825C>T (p.Ser275=)
c.759C>T (p.Ser253=)
17g.17793774T>ACA398546280RAI1c.826T>A (p.Tyr276Asn)
c.760T>A (p.Tyr254Asn)
17g.17793774T>CCA398546281RAI1c.826T>C (p.Tyr276His)
c.760T>C (p.Tyr254His)
17g.17793774T>GCA288367284RAI1c.826T>G (p.Tyr276Asp)
c.760T>G (p.Tyr254Asp)
dbSNP
17g.17793774T=CA2250666918RAI1c.826T= (p.Tyr276=)
c.760T= (p.Tyr254=)
17g.17793775A=CA2250666922RAI1c.827A= (p.Tyr276=)
c.761A= (p.Tyr254=)
17g.17793775A>CCA288367285RAI1c.827A>C (p.Tyr276Ser)
c.761A>C (p.Tyr254Ser)
dbSNP
17g.17793775A>GCA398546282RAI1c.827A>G (p.Tyr276Cys)
c.761A>G (p.Tyr254Cys)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.17793775A>TCA398546283RAI1c.827A>T (p.Tyr276Phe)
c.761A>T (p.Tyr254Phe)
ClinVar dbSNP
17g.17793776T>ACA398546284RAI1c.828T>A (p.Tyr276Ter)
c.762T>A (p.Tyr254Ter)
dbSNP gnomAD v2
17g.17793776T>CCA498422961RAI1c.828T>C (p.Tyr276=)
c.762T>C (p.Tyr254=)
17g.17793776T>GCA398546285RAI1c.828T>G (p.Tyr276Ter)
c.762T>G (p.Tyr254Ter)
17g.17793776T=CA2250666926RAI1c.828T= (p.Tyr276=)
c.762T= (p.Tyr254=)
17g.17793776_17793779delinsTGACCA2250666927RAI1c.828_831delinsTGAC (p.Tyr276=)
c.762_765delinsTGAC (p.Tyr254=)
17g.17793777G>ACA398546286RAI1c.829G>A (p.Asp277Asn)
c.763G>A (p.Asp255Asn)
dbSNP gnomAD v2 gnomAD v4
17g.17793777G>CCA398546287RAI1c.829G>C (p.Asp277His)
c.763G>C (p.Asp255His)
dbSNP
17g.17793777G=CA2250666932RAI1c.829G= (p.Asp277=)
c.763G= (p.Asp255=)
17g.17793777G>TCA398546288RAI1c.829G>T (p.Asp277Tyr)
c.763G>T (p.Asp255Tyr)
17g.17793777_17793779delCA726622927RAI1c.829_831del (p.Asp277del)
c.763_765del (p.Asp255del)
dbSNP
17g.17793777_17793780delinsGACCCA2250666931RAI1c.829_832delinsGACC (p.Asp277=)
c.763_766delinsGACC (p.Asp255=)
17g.17793778A=CA2250666945RAI1c.830A= (p.Asp277=)
c.764A= (p.Asp255=)
17g.17793778A>CCA398546289RAI1c.830A>C (p.Asp277Ala)
c.764A>C (p.Asp255Ala)
17g.17793778A>GCA288367286RAI1c.830A>G (p.Asp277Gly)
c.764A>G (p.Asp255Gly)
dbSNP gnomAD v4
17g.17793778A>TCA288367288RAI1c.830A>T (p.Asp277Val)
c.764A>T (p.Asp255Val)
dbSNP
17g.17793779_17793781delCA8418207RAI1c.831_833del (p.Asp277_Gln278delinsGlu)
c.765_767del (p.Asp255_Gln256delinsGlu)
dbSNP ExAC gnomAD v2
17g.17793779_17793805delCA2636388226RAI1c.831_857del (p.Asp277_Gln286delinsGlu)
c.765_791del (p.Asp255_Gln264delinsGlu)
gnomAD v4
17g.17793778_17793779insGACCA2695224467RAI1c.830_831insGAC (p.Asp277delinsGluThr)
c.764_765insGAC (p.Asp255delinsGluThr)
17g.17793779C>ACA398546290RAI1c.831C>A (p.Asp277Glu)
c.765C>A (p.Asp255Glu)
17g.17793779C=CA2250666955RAI1c.831C= (p.Asp277=)
c.765C= (p.Asp255=)
17g.17793779C>GCA398546291RAI1c.831C>G (p.Asp277Glu)
c.765C>G (p.Asp255Glu)
ClinVar gnomAD v4
17g.17793779C>TCA498422968RAI1c.831C>T (p.Asp277=)
c.765C>T (p.Asp255=)
17g.17793779_17793782delinsCCAGCA2497029353RAI1c.831_834delinsCCAG (p.Asp277=)
c.765_768delinsCCAG (p.Asp255=)
17g.17793779_17793791delinsCCAGCAGCAGCAGCA2573050279RAI1c.831_843delinsCCAGCAGCAGCAG (p.Asp277=)
c.765_777delinsCCAGCAGCAGCAG (p.Asp255=)
17g.17793779_17793806delinsCCAGCAGCAGCAGCAGCAGCAGCAGCAGCA2250666951RAI1c.831_858delinsCCAGCAGCAGCAGCAGCAGCAGCAGCAG (p.Asp277=)
c.765_792delinsCCAGCAGCAGCAGCAGCAGCAGCAGCAG (p.Asp255=)
17g.17793779_17793780insGCAGCAGCAGCACA2250667066RAI1c.831_832insGCAGCAGCAGCA (p.Asp277_Gln278insAlaAlaAlaAla)
c.765_766insGCAGCAGCAGCA (p.Asp255_Gln256insAlaAlaAlaAla)
dbSNP
17g.17793780C>ACA398546292RAI1c.832C>A (p.Gln278Lys)
c.766C>A (p.Gln256Lys)
dbSNP gnomAD v2
17g.17793780C=CA2250667068RAI1c.832C= (p.Gln278=)
c.766C= (p.Gln256=)
17g.17793780C>GCA398546293RAI1c.832C>G (p.Gln278Glu)
c.766C>G (p.Gln256Glu)
17g.17793780C>TCA398546294RAI1c.832C>T (p.Gln278Ter)
c.766C>T (p.Gln256Ter)
17g.17793780_17793781insGGCCA2636388229RAI1c.832_833insGGC (p.Asp277_Gln278insArg)
c.766_767insGGC (p.Asp255_Gln256insArg)
gnomAD v4
17g.17793780_17793781insTGCAGCAGCAGCAGCAGCAGCCA2636388228RAI1c.832_833insTGCAGCAGCAGCAGCAGCAGC (p.Asp277_Gln278insLeuGlnGlnGlnGlnGlnGln)
c.766_767insTGCAGCAGCAGCAGCAGCAGC (p.Asp255_Gln256insLeuGlnGlnGlnGlnGlnGln)
gnomAD v4
17g.17793780_17793781insTGCAGCAGCAGCAGCAGCAGCAGCCA2636388227RAI1c.832_833insTGCAGCAGCAGCAGCAGCAGCAGC (p.Asp277_Gln278insLeuGlnGlnGlnGlnGlnGlnGln)
c.766_767insTGCAGCAGCAGCAGCAGCAGCAGC (p.Asp255_Gln256insLeuGlnGlnGlnGlnGlnGlnGln)
gnomAD v4
17g.17793784_17793785insACAGCACA726623080RAI1c.836_837insACAGCA (p.Gln279_Gln280insGlnGln)
c.770_771insACAGCA (p.Gln257_Gln258insGlnGln)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793784_17793785insACAGCAGCACA2250667064RAI1c.836_837insACAGCAGCA (p.Gln279_Gln280insGlnGlnGln)
c.770_771insACAGCAGCA (p.Gln257_Gln258insGlnGlnGln)
dbSNP gnomAD v4
17g.17793784_17793785insACAGCAGCAGCACA726623075RAI1c.836_837insACAGCAGCAGCA (p.Gln279_Gln280insGlnGlnGlnGln)
c.770_771insACAGCAGCAGCA (p.Gln257_Gln258insGlnGlnGlnGln)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793784_17793785insACAGCAGCAGCAGCACA2739267245RAI1c.836_837insACAGCAGCAGCAGCA (p.Gln279_Gln280insGlnGlnGlnGlnGln)
c.770_771insACAGCAGCAGCAGCA (p.Gln257_Gln258insGlnGlnGlnGlnGln)
ClinVar
17g.17793818_17793820dupCA202432RAI1c.870_872dup (p.Gln291_Ala292insGln)
c.804_806dup (p.Gln269_Ala270insGln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793815_17793820dupCA726623066RAI1c.867_872dup (p.Gln291_Ala292insGlnGln)
c.801_806dup (p.Gln269_Ala270insGlnGln)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793812_17793820dupCA498422995RAI1c.864_872dup (p.Gln291_Ala292insGlnGlnGln)
c.798_806dup (p.Gln269_Ala270insGlnGlnGln)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793809_17793820dupCA206373RAI1c.861_872dup (p.Gln291_Ala292insGlnGlnGlnGln)
c.795_806dup (p.Gln269_Ala270insGlnGlnGlnGln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793806_17793820dupCA726623062RAI1c.858_872dup (p.Gln291_Ala292insGlnGlnGlnGlnGln)
c.792_806dup (p.Gln269_Ala270insGlnGlnGlnGlnGln)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793803_17793820dupCA981957230RAI1c.855_872dup (p.Gln291_Ala292insGlnGlnGlnGlnGlnGln)
c.789_806dup (p.Gln269_Ala270insGlnGlnGlnGlnGlnGln)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793800_17793820dupCA726623055RAI1c.852_872dup (p.Gln291_Ala292insGlnGlnGlnGlnGlnGlnGln)
c.786_806dup (p.Gln269_Ala270insGlnGlnGlnGlnGlnGlnGln)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793797_17793820dupCA981957228RAI1c.849_872dup (p.Gln291_Ala292insGlnGlnGlnGlnGlnGlnGlnGln)
c.783_806dup (p.Gln269_Ala270insGlnGlnGlnGlnGlnGlnGlnGln)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793794_17793820dupCA726623053RAI1c.846_872dup (p.Gln291_Ala292insGlnGlnGlnGlnGlnGlnGlnGlnGln)
c.780_806dup (p.Gln269_Ala270insGlnGlnGlnGlnGlnGlnGlnGlnGln)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793791_17793820dupCA2580614026RAI1c.843_872dup (p.Gln291_Ala292insGlnGlnGlnGlnGlnGlnGlnGlnGlnGln)
c.777_806dup (p.Gln269_Ala270insGlnGlnGlnGlnGlnGlnGlnGlnGlnGln)
ClinVar dbSNP gnomAD v4
17g.17793788_17793820dupCA2591161006RAI1c.840_872dup (p.Gln291_Ala292insGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGln)
c.774_806dup (p.Gln269_Ala270insGlnGlnGlnGlnGlnGlnGlnGlnGlnGlnGln)
gnomAD v3 gnomAD v4
17g.17793818_17793820delCA185914RAI1c.870_872del (p.Gln291del)
c.804_806del (p.Gln269del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.17793815_17793820delCA208708RAI1c.867_872del (p.Gln290_Gln291del)
c.801_806del (p.Gln268_Gln269del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.17793812_17793820delCA202438RAI1c.864_872del (p.Gln289_Gln291del)
c.798_806del (p.Gln267_Gln269del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793809_17793820delCA180361RAI1c.861_872del (p.Gln288_Gln291del)
c.795_806del (p.Gln266_Gln269del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
17g.17793806_17793820delCA498423000RAI1c.858_872del (p.Gln287_Gln291del)
c.792_806del (p.Gln265_Gln269del)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793803_17793820delCA726623096RAI1c.855_872del (p.Gln286_Gln291del)
c.789_806del (p.Gln264_Gln269del)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793800_17793820delCA223811RAI1c.852_872del (p.Gln285_Gln291del)
c.786_806del (p.Gln263_Gln269del)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793797_17793820delCA726623085RAI1c.849_872del (p.Gln284_Gln291del)
c.783_806del (p.Gln262_Gln269del)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.17793794_17793820delCA726623008RAI1c.846_872del (p.Gln283_Gln291del)
c.780_806del (p.Gln261_Gln269del)
ClinVar dbSNP gnomAD v4
17g.17793781delCA625314482RAI1c.833del (p.Gln278ArgfsTer?)
c.767del (p.Gln256ArgfsTer?)
gnomAD v2 gnomAD v4
17g.17793781A=CA2250667138RAI1c.833A= (p.Gln278=)
c.767A= (p.Gln256=)
17g.17793781A>CCA398546297RAI1c.833A>C (p.Gln278Pro)
c.767A>C (p.Gln256Pro)
dbSNP gnomAD v2
17g.17793781A>GCA398546296RAI1c.833A>G (p.Gln278Arg)
c.767A>G (p.Gln256Arg)
17g.17793781A>TCA398546295RAI1c.833A>T (p.Gln278Leu)
c.767A>T (p.Gln256Leu)
17g.17793781_17793782delCA645589909RAI1c.833_834del (p.Gln278ProfsTer?)
c.767_768del (p.Gln256ProfsTer?)
COSMIC COSMIC
17g.17793781_17793782delinsAGCA2250667137RAI1c.833_834delinsAG (p.Gln278=)
c.767_768delinsAG (p.Gln256=)
17g.17793782delCA625314483RAI1c.834del (p.Gln278HisfsTer?)
c.768del (p.Gln256HisfsTer?)
dbSNP gnomAD v2
17g.17793782G>ACA498423006RAI1c.834G>A (p.Gln278=)
c.768G>A (p.Gln256=)
dbSNP gnomAD v2
17g.17793782G>CCA8418209RAI1c.834G>C (p.Gln278His)
c.768G>C (p.Gln256His)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.17793782G=CA2250667149RAI1c.834G= (p.Gln278=)
c.768G= (p.Gln256=)
17g.17793782G>TCA398546298RAI1c.834G>T (p.Gln278His)
c.768G>T (p.Gln256His)
17g.17793782_17793784delinsGCACA2250667146RAI1c.834_836delinsGCA (p.Gln278=)
c.768_770delinsGCA (p.Gln256=)
17g.17793783C>ACA398546299RAI1c.835C>A (p.Gln279Lys)
c.769C>A (p.Gln257Lys)
17g.17793783C=CA2250667163RAI1c.835C= (p.Gln279=)
c.769C= (p.Gln257=)
17g.17793783C>GCA398546300RAI1c.835C>G (p.Gln279Glu)
c.769C>G (p.Gln257Glu)
17g.17793783C>TCA398546301RAI1c.835C>T (p.Gln279Ter)
c.769C>T (p.Gln257Ter)
gnomAD v2
17g.17793783_17793784delCA625314484RAI1c.835_836del (p.Gln279AlafsTer?)
c.769_770del (p.Gln257AlafsTer?)
dbSNP gnomAD v2 gnomAD v4
17g.17793784_17793785insACACA8418208RAI1c.836_837insACA (p.Gln279_Gln280insGln)
c.770_771insACA (p.Gln257_Gln258insGln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793784_17793785insTCACA2636388230RAI1c.836_837insTCA (p.Gln278_Gln279insHis)
c.770_771insTCA (p.Gln256_Gln257insHis)
gnomAD v4
17g.17793783_17793785delinsCAGCA2250667159RAI1c.835_837delinsCAG (p.Gln279=)
c.769_771delinsCAG (p.Gln257=)
17g.17793783_17793791delinsCAGCAGCAGCA2250667165RAI1c.835_843delinsCAGCAGCAG (p.Gln279=)
c.769_777delinsCAGCAGCAG (p.Gln257=)
17g.17793784A=CA2250667182RAI1c.836A= (p.Gln279=)
c.770A= (p.Gln257=)
17g.17793784A>CCA398546303RAI1c.836A>C (p.Gln279Pro)
c.770A>C (p.Gln257Pro)
17g.17793784A>GCA288367346RAI1c.836A>G (p.Gln279Arg)
c.770A>G (p.Gln257Arg)
dbSNP
17g.17793784A>TCA398546302RAI1c.836A>T (p.Gln279Leu)
c.770A>T (p.Gln257Leu)
17g.17793784_17793785delCA231440RAI1c.836_837del (p.Gln279ProfsTer?)
c.770_771del (p.Gln257ProfsTer?)
ClinVar dbSNP
17g.17793785_17793786insGAGCA625314485RAI1c.837_838insGAG (p.Gln279_Gln280insGlu)
c.771_772insGAG (p.Gln257_Gln258insGlu)
dbSNP gnomAD v2 gnomAD v4
17g.17793784_17793786delinsAGCCA2250667178RAI1c.836_838delinsAGC (p.Gln279=)
c.770_772delinsAGC (p.Gln257=)
17g.17793784_17793791delCA2250667184RAI1c.836_843del (p.Gln279ProfsTer?)
c.770_777del (p.Gln257ProfsTer?)
dbSNP
17g.17793785delCA645589910RAI1c.837del (p.Gln279HisfsTer?)
c.771del (p.Gln257HisfsTer?)
COSMIC COSMIC
17g.17793785G>ACA149349RAI1c.837G>A (p.Gln279=)
c.771G>A (p.Gln257=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793785G>CCA398546304RAI1c.837G>C (p.Gln279His)
c.771G>C (p.Gln257His)
dbSNP gnomAD v4
17g.17793785G=CA2250667206RAI1c.837G= (p.Gln279=)
c.771G= (p.Gln257=)
17g.17793785G>TCA398546305RAI1c.837G>T (p.Gln279His)
c.771G>T (p.Gln257His)
17g.17793785_17793786delCA180360RAI1c.837_838del (p.Gln280AlafsTer?)
c.771_772del (p.Gln258AlafsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
17g.17793785_17793789delinsATCA2580092640RAI1c.837_841delinsAT (p.Gln280Ter)
c.771_775delinsAT (p.Gln258Ter)
ClinVar dbSNP
17g.17793785_17793797delinsACA2499223928RAI1c.837_849delinsA (p.Gln280_Gln283del)
c.771_783delinsA (p.Gln258_Gln261del)
ClinVar dbSNP
17g.17793786C>ACA288367354RAI1c.838C>A (p.Gln280Lys)
c.772C>A (p.Gln258Lys)
dbSNP
17g.17793786C=CA2250667213RAI1c.838C= (p.Gln280=)
c.772C= (p.Gln258=)
17g.17793786C>GCA398546307RAI1c.838C>G (p.Gln280Glu)
c.772C>G (p.Gln258Glu)
17g.17793786C>TCA398546306RAI1c.838C>T (p.Gln280Ter)
c.772C>T (p.Gln258Ter)
17g.17793786_17793787insCAGCAGCA645373073RAI1c.838_839insCAGCAG (p.Gln280delinsProAlaGlu)
c.772_773insCAGCAG (p.Gln258delinsProAlaGlu)
ClinVar dbSNP
17g.17793787A>CCA398546310RAI1c.839A>C (p.Gln280Pro)
c.773A>C (p.Gln258Pro)
17g.17793787A>GCA398546308RAI1c.839A>G (p.Gln280Arg)
c.773A>G (p.Gln258Arg)
17g.17793787A>TCA398546309RAI1c.839A>T (p.Gln280Leu)
c.773A>T (p.Gln258Leu)
17g.17793787_17793788delinsAGCA2250667237RAI1c.839_840delinsAG (p.Gln280=)
c.773_774delinsAG (p.Gln258=)
17g.17793787_17793789delinsAGCCA2250667234RAI1c.839_841delinsAGC (p.Gln280=)
c.773_775delinsAGC (p.Gln258=)
17g.17793787_17793791delinsAGCAGCA2250667231RAI1c.839_843delinsAGCAG (p.Gln280=)
c.773_777delinsAGCAG (p.Gln258=)
17g.17793787_17793794delinsAGCAGCAGCA2250667228RAI1c.839_846delinsAGCAGCAG (p.Gln280=)
c.773_780delinsAGCAGCAG (p.Gln258=)
17g.17793787_17793797delinsAGCAGCAGCAGCA2250667226RAI1c.839_849delinsAGCAGCAGCAG (p.Gln280=)
c.773_783delinsAGCAGCAGCAG (p.Gln258=)
17g.17793787_17793800delinsAGCAGCAGCAGCAGCA2250667229RAI1c.839_852delinsAGCAGCAGCAGCAG (p.Gln280=)
c.773_786delinsAGCAGCAGCAGCAG (p.Gln258=)
17g.17793787_17793803delinsAGCAGCAGCAGCAGCAGCA2250667224RAI1c.839_855delinsAGCAGCAGCAGCAGCAG (p.Gln280=)
c.773_789delinsAGCAGCAGCAGCAGCAG (p.Gln258=)
17g.17793788delCA8418210RAI1c.840del (p.Gln280HisfsTer?)
c.774del (p.Gln258HisfsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
17g.17793788G>ACA149351RAI1c.840G>A (p.Gln280=)
c.774G>A (p.Gln258=)
ClinVar dbSNP ExAC gnomAD v2
17g.17793788G>CCA398546311RAI1c.840G>C (p.Gln280His)
c.774G>C (p.Gln258His)
dbSNP
17g.17793788G=CA2250667275RAI1c.840G= (p.Gln280=)
c.774G= (p.Gln258=)
17g.17793788G>TCA398546312RAI1c.840G>T (p.Gln280His)
c.774G>T (p.Gln258His)
dbSNP
17g.17793788_17793789delCA288367367RAI1c.840_841del (p.Gln281AlafsTer?)
c.774_775del (p.Gln259AlafsTer?)
dbSNP
17g.17793788_17793791delCA8418211RAI1c.840_843del (p.Gln280HisfsTer?)
c.774_777del (p.Gln258HisfsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793788_17793794delCA8418213RAI1c.840_846del (p.Gln280HisfsTer?)
c.774_780del (p.Gln258HisfsTer?)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793788_17793797delCA8418212RAI1c.840_849del (p.Gln280HisfsTer?)
c.774_783del (p.Gln258HisfsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793788_17793800delCA8418214RAI1c.840_852del (p.Gln280HisfsTer?)
c.774_786del (p.Gln258HisfsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793788_17793803delCA8418215RAI1c.840_855del (p.Gln280HisfsTer?)
c.774_789del (p.Gln258HisfsTer?)
dbSNP ExAC gnomAD v3 gnomAD v4
17g.17793788_17793806delCA2591161015RAI1c.840_858del (p.Gln280HisfsTer?)
c.774_792del (p.Gln258HisfsTer?)
gnomAD v3 gnomAD v4
17g.17793789C>ACA398546313RAI1c.841C>A (p.Gln281Lys)
c.775C>A (p.Gln259Lys)
17g.17793789C=CA2250667311RAI1c.841C= (p.Gln281=)
c.775C= (p.Gln259=)
17g.17793789C>GCA398546314RAI1c.841C>G (p.Gln281Glu)
c.775C>G (p.Gln259Glu)
17g.17793789C>TCA398546315RAI1c.841C>T (p.Gln281Ter)
c.775C>T (p.Gln259Ter)
dbSNP gnomAD v2
17g.17793790_17793791insACACA2636388231RAI1c.842_843insACA (p.Gln281_Gln282insGln)
c.776_777insACA (p.Gln259_Gln260insGln)
gnomAD v4
17g.17793789_17793792delCA625314486RAI1c.841_844del (p.Gln281SerfsTer?)
c.775_778del (p.Gln259SerfsTer?)
gnomAD v2
17g.17793793_17793794insACAGCACA2636388232RAI1c.845_846insACAGCA (p.Gln282_Gln283insGlnGln)
c.779_780insACAGCA (p.Gln260_Gln261insGlnGln)
gnomAD v4
17g.17793796_17793797insACAGCAGCACA2250667308RAI1c.848_849insACAGCAGCA (p.Gln283_Gln284insGlnGlnGln)
c.782_783insACAGCAGCA (p.Gln261_Gln262insGlnGlnGln)
dbSNP
17g.17793799_17793800insACAGCAGCAGCACA891844155RAI1c.851_852insACAGCAGCAGCA (p.Gln284_Gln285insGlnGlnGlnGln)
c.785_786insACAGCAGCAGCA (p.Gln262_Gln263insGlnGlnGlnGln)
ClinVar dbSNP gnomAD v4
17g.17793790A>CCA398546316RAI1c.842A>C (p.Gln281Pro)
c.776A>C (p.Gln259Pro)
17g.17793790A>GCA398546317RAI1c.842A>G (p.Gln281Arg)
c.776A>G (p.Gln259Arg)
17g.17793790A>TCA398546318RAI1c.842A>T (p.Gln281Leu)
c.776A>T (p.Gln259Leu)
17g.17793790_17793791delinsAGCA2250667315RAI1c.842_843delinsAG (p.Gln281=)
c.776_777delinsAG (p.Gln259=)
17g.17793791delCA625314487RAI1c.843del (p.Gln281HisfsTer?)
c.777del (p.Gln259HisfsTer?)
dbSNP gnomAD v2
17g.17793791G>ACA8418216RAI1c.843G>A (p.Gln281=)
c.777G>A (p.Gln259=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
17g.17793791G>CCA398546319RAI1c.843G>C (p.Gln281His)
c.777G>C (p.Gln259His)
dbSNP
17g.17793791G=CA2250667322RAI1c.843G= (p.Gln281=)
c.777G= (p.Gln259=)
17g.17793791G>TCA398546320RAI1c.843G>T (p.Gln281His)
c.777G>T (p.Gln259His)
17g.17793792C>ACA398546321RAI1c.844C>A (p.Gln282Lys)
c.778C>A (p.Gln260Lys)
17g.17793792C>GCA398546322RAI1c.844C>G (p.Gln282Glu)
c.778C>G (p.Gln260Glu)
17g.17793792C>TCA398546323RAI1c.844C>T (p.Gln282Ter)
c.778C>T (p.Gln260Ter)
17g.17793793delCA2636388233RAI1c.845del (p.Gln282ArgfsTer?)
c.779del (p.Gln260ArgfsTer?)
gnomAD v4
17g.17793793A=CA2250667330RAI1c.845A= (p.Gln282=)
c.779A= (p.Gln260=)
17g.17793793A>CCA398546324RAI1c.845A>C (p.Gln282Pro)
c.779A>C (p.Gln260Pro)
17g.17793793A>GCA398546325RAI1c.845A>G (p.Gln282Arg)
c.779A>G (p.Gln260Arg)
dbSNP gnomAD v2
17g.17793793A>TCA398546326RAI1c.845A>T (p.Gln282Leu)
c.779A>T (p.Gln260Leu)
17g.17793794G>ACA288367383RAI1c.846G>A (p.Gln282=)
c.780G>A (p.Gln260=)
ClinVar dbSNP gnomAD v2 COSMIC COSMIC
17g.17793794G>CCA398546328RAI1c.846G>C (p.Gln282His)
c.780G>C (p.Gln260His)
17g.17793794G=CA2250667337RAI1c.846G= (p.Gln282=)
c.780G= (p.Gln260=)
17g.17793794G>TCA398546327RAI1c.846G>T (p.Gln282His)
c.780G>T (p.Gln260His)
17g.17793795C>ACA398546329RAI1c.847C>A (p.Gln283Lys)
c.781C>A (p.Gln261Lys)
gnomAD v4
17g.17793795C=CA2250667340RAI1c.847C= (p.Gln283=)
c.781C= (p.Gln261=)
17g.17793795C>GCA398546330RAI1c.847C>G (p.Gln283Glu)
c.781C>G (p.Gln261Glu)
17g.17793795C>TCA398546331RAI1c.847C>T (p.Gln283Ter)
c.781C>T (p.Gln261Ter)
ClinVar dbSNP
17g.17793795_17793805delCA2636388234RAI1c.847_857del (p.Gln283AlafsTer?)
c.781_791del (p.Gln261AlafsTer?)
gnomAD v4
17g.17793796A>CCA398546332RAI1c.848A>C (p.Gln283Pro)
c.782A>C (p.Gln261Pro)
17g.17793796A>GCA398546333RAI1c.848A>G (p.Gln283Arg)
c.782A>G (p.Gln261Arg)
17g.17793796A>TCA398546334RAI1c.848A>T (p.Gln283Leu)
c.782A>T (p.Gln261Leu)
17g.17793796_17793798delinsAGCCA2250667345RAI1c.848_850delinsAGC (p.Gln283=)
c.782_784delinsAGC (p.Gln261=)
17g.17793796_17793799delCA2580092641RAI1c.848_851del (p.Gln283ArgfsTer?)
c.782_785del (p.Gln261ArgfsTer?)
ClinVar
17g.17793803_17793804insAAGCAGCAGCA2636388235RAI1c.855_856insAAGCAGCAG (p.Gln285_Gln286insLysGlnGln)
c.789_790insAAGCAGCAG (p.Gln263_Gln264insLysGlnGln)
gnomAD v4
17g.17793797G>ACA10604615RAI1c.849G>A (p.Gln283=)
c.783G>A (p.Gln261=)
ClinVar dbSNP gnomAD v2 COSMIC COSMIC
17g.17793797G>CCA398546335RAI1c.849G>C (p.Gln283His)
c.783G>C (p.Gln261His)
17g.17793797G=CA2250667357RAI1c.849G= (p.Gln283=)
c.783G= (p.Gln261=)
17g.17793797G>TCA398546336RAI1c.849G>T (p.Gln283His)
c.783G>T (p.Gln261His)
17g.17793797_17793798delCA625314488RAI1c.849_850del (p.Gln284AlafsTer?)
c.783_784del (p.Gln262AlafsTer?)
dbSNP gnomAD v2
17g.17793798C>ACA398546339RAI1c.850C>A (p.Gln284Lys)
c.784C>A (p.Gln262Lys)
17g.17793798C>GCA398546338RAI1c.850C>G (p.Gln284Glu)
c.784C>G (p.Gln262Glu)
17g.17793798C>TCA398546337RAI1c.850C>T (p.Gln284Ter)
c.784C>T (p.Gln262Ter)
17g.17793799A>CCA398546340RAI1c.851A>C (p.Gln284Pro)
c.785A>C (p.Gln262Pro)
17g.17793799A>GCA398546341RAI1c.851A>G (p.Gln284Arg)
c.785A>G (p.Gln262Arg)
17g.17793799A>TCA398546342RAI1c.851A>T (p.Gln284Leu)
c.785A>T (p.Gln262Leu)
17g.17793800G>ACA288367387RAI1c.852G>A (p.Gln284=)
c.786G>A (p.Gln262=)
ClinVar dbSNP
17g.17793800G>CCA398546343RAI1c.852G>C (p.Gln284His)
c.786G>C (p.Gln262His)
ClinVar dbSNP
17g.17793800G=CA2250667361RAI1c.852G= (p.Gln284=)
c.786G= (p.Gln262=)
17g.17793800G>TCA398546344RAI1c.852G>T (p.Gln284His)
c.786G>T (p.Gln262His)
17g.17793801_17793802insGGCCA2739267246RAI1c.853_854insGGC (p.Gln284_Gln285insArg)
c.787_788insGGC (p.Gln262_Gln263insArg)
ClinVar
17g.17793801C>ACA398546345RAI1c.853C>A (p.Gln285Lys)
c.787C>A (p.Gln263Lys)
17g.17793801C=CA2250667366RAI1c.853C= (p.Gln285=)
c.787C= (p.Gln263=)
17g.17793801C>GCA398546346RAI1c.853C>G (p.Gln285Glu)
c.787C>G (p.Gln263Glu)
17g.17793801C>TCA8418217RAI1c.853C>T (p.Gln285Ter)
c.787C>T (p.Gln263Ter)
ClinVar dbSNP ExAC
17g.17793802A=CA2250667373RAI1c.854A= (p.Gln285=)
c.788A= (p.Gln263=)
17g.17793802A>CCA398546347RAI1c.854A>C (p.Gln285Pro)
c.788A>C (p.Gln263Pro)
dbSNP gnomAD v2
17g.17793802A>GCA8418218RAI1c.854A>G (p.Gln285Arg)
c.788A>G (p.Gln263Arg)
dbSNP ExAC
17g.17793802A>TCA398546348RAI1c.854A>T (p.Gln285Leu)
c.788A>T (p.Gln263Leu)
17g.17793803G>ACA498423053RAI1c.855G>A (p.Gln285=)
c.789G>A (p.Gln263=)
ClinVar dbSNP
17g.17793803G>CCA398546349RAI1c.855G>C (p.Gln285His)
c.789G>C (p.Gln263His)
17g.17793803G=CA2250667383RAI1c.855G= (p.Gln285=)
c.789G= (p.Gln263=)
17g.17793803G>TCA8418219RAI1c.855G>T (p.Gln285His)
c.789G>T (p.Gln263His)
dbSNP ExAC
17g.17793803_17793804delCA2636388236RAI1c.855_856del (p.Gln286AlafsTer?)
c.789_790del (p.Gln264AlafsTer?)
gnomAD v4
17g.17793804C>ACA398546351RAI1c.856C>A (p.Gln286Lys)
c.790C>A (p.Gln264Lys)
17g.17793804C=CA2250667387RAI1c.856C= (p.Gln286=)
c.790C= (p.Gln264=)
17g.17793804C>GCA398546352RAI1c.856C>G (p.Gln286Glu)
c.790C>G (p.Gln264Glu)
17g.17793804C>TCA398546350RAI1c.856C>T (p.Gln286Ter)
c.790C>T (p.Gln264Ter)
ClinVar gnomAD v4
17g.17793805A>CCA398546353RAI1c.857A>C (p.Gln286Pro)
c.791A>C (p.Gln264Pro)
17g.17793805A>GCA398546354RAI1c.857A>G (p.Gln286Arg)
c.791A>G (p.Gln264Arg)
17g.17793805A>TCA398546355RAI1c.857A>T (p.Gln286Leu)
c.791A>T (p.Gln264Leu)
17g.17793805_17793806insTTAAGACA625314489RAI1c.857_858insTTAAGA (p.Gln286HisfsTer2)
c.791_792insTTAAGA (p.Gln264HisfsTer2)
dbSNP gnomAD v2
17g.17793806G>ACA498423063RAI1c.858G>A (p.Gln286=)
c.792G>A (p.Gln264=)
dbSNP
17g.17793806G>CCA398546356RAI1c.858G>C (p.Gln286His)
c.792G>C (p.Gln264His)
17g.17793806G=CA2250667393RAI1c.858G= (p.Gln286=)
c.792G= (p.Gln264=)
17g.17793806G>TCA8418220RAI1c.858G>T (p.Gln286His)
c.792G>T (p.Gln264His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.17793806_17793809delCA2636388237RAI1c.858_861del (p.Gln286HisfsTer?)
c.792_795del (p.Gln264HisfsTer?)
gnomAD v4
17g.17793807C>ACA398546358RAI1c.859C>A (p.Gln287Lys)
c.793C>A (p.Gln265Lys)
17g.17793807C=CA2250667412RAI1c.859C= (p.Gln287=)
c.793C= (p.Gln265=)
17g.17793807C>GCA398546360RAI1c.859C>G (p.Gln287Glu)
c.793C>G (p.Gln265Glu)
17g.17793807C>TCA398546357RAI1c.859C>T (p.Gln287Ter)
c.793C>T (p.Gln265Ter)
ClinVar dbSNP
17g.17793808A=CA2250667421RAI1c.860A= (p.Gln287=)
c.794A= (p.Gln265=)
17g.17793808A>CCA398546363RAI1c.860A>C (p.Gln287Pro)
c.794A>C (p.Gln265Pro)
17g.17793808A>GCA398546362RAI1c.860A>G (p.Gln287Arg)
c.794A>G (p.Gln265Arg)
17g.17793808A>TCA8418221RAI1c.860A>T (p.Gln287Leu)
c.794A>T (p.Gln265Leu)
dbSNP ExAC
17g.17793808_17793809delCA2573054335RAI1c.860_861del (p.Gln287ProfsTer?)
c.794_795del (p.Gln265ProfsTer?)
ClinVar dbSNP
17g.17793808_17793830delinsAGCAGCAGCAGCAAGCCCTTCAGCA2250667420RAI1c.860_882delinsAGCAGCAGCAGCAAGCCCTTCAG (p.Gln287=)
c.794_816delinsAGCAGCAGCAGCAAGCCCTTCAG (p.Gln265=)
17g.17793809G>ACA498423068RAI1c.861G>A (p.Gln287=)
c.795G>A (p.Gln265=)
17g.17793809G>CCA398546364RAI1c.861G>C (p.Gln287His)
c.795G>C (p.Gln265His)
17g.17793809G>TCA398546365RAI1c.861G>T (p.Gln287His)
c.795G>T (p.Gln265His)
17g.17793809_17793830delinsAGCCCTTCAACA891844156RAI1c.861_882delinsAGCCCTTCAA (p.Gln288_Gln291del)
c.795_816delinsAGCCCTTCAA (p.Gln266_Gln269del)
ClinVar dbSNP
17g.17793810C>ACA398546368RAI1c.862C>A (p.Gln288Lys)
c.796C>A (p.Gln266Lys)
17g.17793810C>GCA398546367RAI1c.862C>G (p.Gln288Glu)
c.796C>G (p.Gln266Glu)
17g.17793810C>TCA398546366RAI1c.862C>T (p.Gln288Ter)
c.796C>T (p.Gln266Ter)
17g.17793811A>CCA398546369RAI1c.863A>C (p.Gln288Pro)
c.797A>C (p.Gln266Pro)
17g.17793811A>GCA398546371RAI1c.863A>G (p.Gln288Arg)
c.797A>G (p.Gln266Arg)
17g.17793811A>TCA398546370RAI1c.863A>T (p.Gln288Leu)
c.797A>T (p.Gln266Leu)
17g.17793812G>ACA498423073RAI1c.864G>A (p.Gln288=)
c.798G>A (p.Gln266=)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
17g.17793812G>CCA398546373RAI1c.864G>C (p.Gln288His)
c.798G>C (p.Gln266His)
17g.17793812G>TCA398546372RAI1c.864G>T (p.Gln288His)
c.798G>T (p.Gln266His)
17g.17793813C>ACA398546376RAI1c.865C>A (p.Gln289Lys)
c.799C>A (p.Gln267Lys)
17g.17793813C>GCA398546374RAI1c.865C>G (p.Gln289Glu)
c.799C>G (p.Gln267Glu)
17g.17793813C>TCA398546375RAI1c.865C>T (p.Gln289Ter)
c.799C>T (p.Gln267Ter)
gnomAD v2
17g.17793820_17793821insGCAACAGCAGCACA912999130RAI1c.872_873insGCAACAGCAGCA (p.Gln291_Ala292insGlnGlnGlnGln)
c.806_807insGCAACAGCAGCA (p.Gln269_Ala270insGlnGlnGlnGln)
17g.17793813_17793821delCA2636388238RAI1c.865_873del (p.Gln289_Gln291del)
c.799_807del (p.Gln267_Gln269del)
gnomAD v4
17g.17793814A>CCA398546377RAI1c.866A>C (p.Gln289Pro)
c.800A>C (p.Gln267Pro)
17g.17793814A>GCA398546378RAI1c.866A>G (p.Gln289Arg)
c.800A>G (p.Gln267Arg)
17g.17793814A>TCA398546379RAI1c.866A>T (p.Gln289Leu)
c.800A>T (p.Gln267Leu)
17g.17793814_17793816delinsAGCCA2250667439RAI1c.866_868delinsAGC (p.Gln289=)
c.800_802delinsAGC (p.Gln267=)
17g.17793817_17793823delCA625314490RAI1c.869_875del (p.Gln290ProfsTer?)
c.803_809del (p.Gln268ProfsTer?)
gnomAD v2
17g.17793815G>ACA8418222RAI1c.867G>A (p.Gln289=)
c.801G>A (p.Gln267=)
ClinVar dbSNP ExAC
17g.17793815G>CCA398546380RAI1c.867G>C (p.Gln289His)
c.801G>C (p.Gln267His)
17g.17793815G=CA2250667443RAI1c.867G= (p.Gln289=)
c.801G= (p.Gln267=)
17g.17793815G>TCA398546381RAI1c.867G>T (p.Gln289His)
c.801G>T (p.Gln267His)
17g.17793815_17793816delCA625314491RAI1c.867_868del (p.Gln290AlafsTer?)
c.801_802del (p.Gln268AlafsTer?)
dbSNP gnomAD v2
17g.17793815_17793821delinsGCAGCAACA2250667446RAI1c.867_873delinsGCAGCAA (p.Gln289=)
c.801_807delinsGCAGCAA (p.Gln267=)
17g.17793816C>ACA398546382RAI1c.868C>A (p.Gln290Lys)
c.802C>A (p.Gln268Lys)
17g.17793816C=CA2250667457RAI1c.868C= (p.Gln290=)
c.802C= (p.Gln268=)
17g.17793816C>GCA398546383RAI1c.868C>G (p.Gln290Glu)
c.802C>G (p.Gln268Glu)
17g.17793816C>TCA8418223RAI1c.868C>T (p.Gln290Ter)
c.802C>T (p.Gln268Ter)
ClinVar dbSNP ExAC
17g.17793816_17793821delCA625314492RAI1c.868_873del (p.Gln290_Gln291del)
c.802_807del (p.Gln268_Gln269del)
dbSNP gnomAD v2 gnomAD v4
17g.17793817A=CA2250667465RAI1c.869A= (p.Gln290=)
c.803A= (p.Gln268=)
17g.17793817A>CCA398546385RAI1c.869A>C (p.Gln290Pro)
c.803A>C (p.Gln268Pro)
17g.17793817A>GCA8418224RAI1c.869A>G (p.Gln290Arg)
c.803A>G (p.Gln268Arg)
dbSNP ExAC
17g.17793817A>TCA398546384RAI1c.869A>T (p.Gln290Leu)
c.803A>T (p.Gln268Leu)
17g.17793817dupCA288367406RAI1c.869dup (p.Gln291AlafsTer?)
c.803dup (p.Gln269AlafsTer?)
dbSNP
17g.17793818G>ACA498423096RAI1c.870G>A (p.Gln290=)
c.804G>A (p.Gln268=)
dbSNP
17g.17793818G>CCA398546386RAI1c.870G>C (p.Gln290His)
c.804G>C (p.Gln268His)
17g.17793818G=CA2250667478RAI1c.870G= (p.Gln290=)
c.804G= (p.Gln268=)
17g.17793818G>TCA398546387RAI1c.870G>T (p.Gln290His)
c.804G>T (p.Gln268His)
17g.17793818_17793821delinsGCAACA2250667473RAI1c.870_873delinsGCAA (p.Gln290=)
c.804_807delinsGCAA (p.Gln268=)
17g.17793819C>ACA398546389RAI1c.871C>A (p.Gln291Lys)
c.805C>A (p.Gln269Lys)
17g.17793819C>GCA398546390RAI1c.871C>G (p.Gln291Glu)
c.805C>G (p.Gln269Glu)
17g.17793819C>TCA398546388RAI1c.871C>T (p.Gln291Ter)
c.805C>T (p.Gln269Ter)
17g.17793820_17793821insGCAACACA912999131RAI1c.872_873insGCAACA (p.Gln291_Ala292insGlnGln)
c.806_807insGCAACA (p.Gln269_Ala270insGlnGln)
17g.17793819_17793821delCA625314493RAI1c.871_873del (p.Gln291del)
c.805_807del (p.Gln269del)
dbSNP gnomAD v2
17g.17793820A=CA2250667488RAI1c.872A= (p.Gln291=)
c.806A= (p.Gln269=)
17g.17793820A>CCA288367408RAI1c.872A>C (p.Gln291Pro)
c.806A>C (p.Gln269Pro)
dbSNP
17g.17793820A>GCA398546392RAI1c.872A>G (p.Gln291Arg)
c.806A>G (p.Gln269Arg)
17g.17793820A>TCA398546391RAI1c.872A>T (p.Gln291Leu)
c.806A>T (p.Gln269Leu)
17g.17793820_17793821insGCCA2573105829RAI1c.872_873insGC (p.Ala292GlnfsTer?)
c.806_807insGC (p.Ala270GlnfsTer?)
gnomAD v4
17g.17793820_17793821insGCAGCCA8418225RAI1c.872_873insGCAGC (p.Ala292GlnfsTer?)
c.806_807insGCAGC (p.Ala270GlnfsTer?)
dbSNP ExAC gnomAD v2
17g.17793820_17793821insGCAGCAGCCA625314494RAI1c.872_873insGCAGCAGC (p.Ala292GlnfsTer?)
c.806_807insGCAGCAGC (p.Ala270GlnfsTer?)
gnomAD v2 gnomAD v4
17g.17793820_17793821insGCAGCAGCAGCAGCCA2636388239RAI1c.872_873insGCAGCAGCAGCAGC (p.Ala292GlnfsTer?)
c.806_807insGCAGCAGCAGCAGC (p.Ala270GlnfsTer?)
gnomAD v4
17g.17793820_17793821insGCAGCAGCAGCAGCAGCCA2636388240RAI1c.872_873insGCAGCAGCAGCAGCAGC (p.Ala292GlnfsTer?)
c.806_807insGCAGCAGCAGCAGCAGC (p.Ala270GlnfsTer?)
gnomAD v4
17g.17793820_17793821insGCAGCAGCAGCAGCAGCAGCCA2636388241RAI1c.872_873insGCAGCAGCAGCAGCAGCAGC (p.Ala292GlnfsTer?)
c.806_807insGCAGCAGCAGCAGCAGCAGC (p.Ala270GlnfsTer?)
gnomAD v4
17g.17793821A=CA2250667498RAI1c.873A= (p.Gln291=)
c.807A= (p.Gln269=)
17g.17793821A>CCA288367412RAI1c.873A>C (p.Gln291His)
c.807A>C (p.Gln269His)
dbSNP
17g.17793821A>GCA8418226RAI1c.873A>G (p.Gln291=)
c.807A>G (p.Gln269=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.17793821A>TCA398546393RAI1c.873A>T (p.Gln291His)
c.807A>T (p.Gln269His)
17g.17793822G>ACA398546395RAI1c.874G>A (p.Ala292Thr)
c.808G>A (p.Ala270Thr)
17g.17793822G>CCA398546394RAI1c.874G>C (p.Ala292Pro)
c.808G>C (p.Ala270Pro)
17g.17793822G=CA2250667507RAI1c.874G= (p.Ala292=)
c.808G= (p.Ala270=)
17g.17793822G>TCA288367416RAI1c.874G>T (p.Ala292Ser)
c.808G>T (p.Ala270Ser)
dbSNP
17g.17793822dupCA2573105828RAI1c.874dup (p.Ala292GlyfsTer?)
c.808dup (p.Ala270GlyfsTer?)
gnomAD v4
17g.17793823C>ACA398546396RAI1c.875C>A (p.Ala292Asp)
c.809C>A (p.Ala270Asp)
17g.17793823C=CA2250667512RAI1c.875C= (p.Ala292=)
c.809C= (p.Ala270=)
17g.17793823C>GCA8418227RAI1c.875C>G (p.Ala292Gly)
c.809C>G (p.Ala270Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.17793823C>TCA288367419RAI1c.875C>T (p.Ala292Val)
c.809C>T (p.Ala270Val)
dbSNP
17g.17793824C>ACA498423103RAI1c.876C>A (p.Ala292=)
c.810C>A (p.Ala270=)
17g.17793824C>GCA498423104RAI1c.876C>G (p.Ala292=)
c.810C>G (p.Ala270=)
17g.17793824C>TCA498423106RAI1c.876C>T (p.Ala292=)
c.810C>T (p.Ala270=)
17g.17793825C>ACA8418228RAI1c.877C>A (p.Leu293Ile)
c.811C>A (p.Leu271Ile)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
17g.17793825C=CA2250667523RAI1c.877C= (p.Leu293=)
c.811C= (p.Leu271=)
17g.17793825C>GCA398546397RAI1c.877C>G (p.Leu293Val)
c.811C>G (p.Leu271Val)
17g.17793825C>TCA398546398RAI1c.877C>T (p.Leu293Phe)
c.811C>T (p.Leu271Phe)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.17793826T>ACA398546399RAI1c.878T>A (p.Leu293His)
c.812T>A (p.Leu271His)
17g.17793826T>CCA398546400RAI1c.878T>C (p.Leu293Pro)
c.812T>C (p.Leu271Pro)
gnomAD v4
17g.17793826T>GCA398546401RAI1c.878T>G (p.Leu293Arg)
c.812T>G (p.Leu271Arg)
17g.17793827T>ACA498423113RAI1c.879T>A (p.Leu293=)
c.813T>A (p.Leu271=)
17g.17793827T>CCA498423114RAI1c.879T>C (p.Leu293=)
c.813T>C (p.Leu271=)
17g.17793827T>GCA498423115RAI1c.879T>G (p.Leu293=)
c.813T>G (p.Leu271=)
17g.17793828C>ACA398546404RAI1c.880C>A (p.Gln294Lys)
c.814C>A (p.Gln272Lys)
17g.17793828C>GCA398546402RAI1c.880C>G (p.Gln294Glu)
c.814C>G (p.Gln272Glu)
17g.17793828C>TCA398546403RAI1c.880C>T (p.Gln294Ter)
c.814C>T (p.Gln272Ter)
COSMIC COSMIC
17g.17793829A>CCA398546405RAI1c.881A>C (p.Gln294Pro)
c.815A>C (p.Gln272Pro)
17g.17793829A>GCA398546406RAI1c.881A>G (p.Gln294Arg)
c.815A>G (p.Gln272Arg)
17g.17793829A>TCA398546407RAI1c.881A>T (p.Gln294Leu)
c.815A>T (p.Gln272Leu)
17g.17793830G>ACA498423123RAI1c.882G>A (p.Gln294=)
c.816G>A (p.Gln272=)
17g.17793830G>CCA398546408RAI1c.882G>C (p.Gln294His)
c.816G>C (p.Gln272His)
gnomAD v4
17g.17793830G>TCA398546409RAI1c.882G>T (p.Gln294His)
c.816G>T (p.Gln272His)
17g.17793831A=CA2250667527RAI1c.883A= (p.Ser295=)
c.817A= (p.Ser273=)
17g.17793831A>CCA398546410RAI1c.883A>C (p.Ser295Arg)
c.817A>C (p.Ser273Arg)
17g.17793831A>GCA398546411RAI1c.883A>G (p.Ser295Gly)
c.817A>G (p.Ser273Gly)
dbSNP gnomAD v3 gnomAD v4
17g.17793831A>TCA398546412RAI1c.883A>T (p.Ser295Cys)
c.817A>T (p.Ser273Cys)
17g.17793832G>ACA398546413RAI1c.884G>A (p.Ser295Asn)
c.818G>A (p.Ser273Asn)
dbSNP gnomAD v2 gnomAD v4
17g.17793832G>CCA398546414RAI1c.884G>C (p.Ser295Thr)
c.818G>C (p.Ser273Thr)
17g.17793832G=CA2250667529RAI1c.884G= (p.Ser295=)
c.818G= (p.Ser273=)
17g.17793832G>TCA398546415RAI1c.884G>T (p.Ser295Ile)
c.818G>T (p.Ser273Ile)
gnomAD v4
17g.17793833C>ACA398546416RAI1c.885C>A (p.Ser295Arg)
c.819C>A (p.Ser273Arg)
17g.17793833C=CA2250667534RAI1c.885C= (p.Ser295=)
c.819C= (p.Ser273=)
17g.17793833C>GCA398546417RAI1c.885C>G (p.Ser295Arg)
c.819C>G (p.Ser273Arg)
17g.17793833C>TCA498423131RAI1c.885C>T (p.Ser295=)
c.819C>T (p.Ser273=)
dbSNP
17g.17793834C>ACA498423132RAI1c.886C>A (p.Arg296=)
c.820C>A (p.Arg274=)
17g.17793834C=CA2250667539RAI1c.886C= (p.Arg296=)
c.820C= (p.Arg274=)
17g.17793834C>GCA398546418RAI1c.886C>G (p.Arg296Gly)
c.820C>G (p.Arg274Gly)
17g.17793834C>TCA8418229RAI1c.886C>T (p.Arg296Trp)
c.820C>T (p.Arg274Trp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793835G>ACA8418230RAI1c.887G>A (p.Arg296Gln)
c.821G>A (p.Arg274Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.17793835G>CCA398546419RAI1c.887G>C (p.Arg296Pro)
c.821G>C (p.Arg274Pro)
gnomAD v4
17g.17793835G=CA2250667545RAI1c.887G= (p.Arg296=)
c.821G= (p.Arg274=)
17g.17793835G>TCA398546420RAI1c.887G>T (p.Arg296Leu)
c.821G>T (p.Arg274Leu)
COSMIC COSMIC
17g.17793836G>ACA498423134RAI1c.888G>A (p.Arg296=)
c.822G>A (p.Arg274=)
17g.17793836G>CCA498423135RAI1c.888G>C (p.Arg296=)
c.822G>C (p.Arg274=)
17g.17793836G>TCA498423137RAI1c.888G>T (p.Arg296=)
c.822G>T (p.Arg274=)

Number of alleles fetched