Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.74740856C>ACA413664938NEXMIFc.3701G>T (p.Gly1234Val)
Xg.74740856C=CA2437590142NEXMIFc.3701G= (p.Gly1234=)
Xg.74740856C>GCA413664939NEXMIFc.3701G>C (p.Gly1234Ala)
Xg.74740856C>TCA10454919NEXMIFc.3701G>A (p.Gly1234Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74740857C>ACA413664940NEXMIFc.3700G>T (p.Gly1234Ter)
ClinVar dbSNP
Xg.74740857C=CA2437590143NEXMIFc.3700G= (p.Gly1234=)
Xg.74740857C>GCA413664942NEXMIFc.3700G>C (p.Gly1234Arg)
Xg.74740857C>TCA413664941NEXMIFc.3700G>A (p.Gly1234Arg)
dbSNP gnomAD v2 gnomAD v4
Xg.74740858A=CA2437590144NEXMIFc.3699T= (p.Asn1233=)
Xg.74740858A>CCA413664943NEXMIFc.3699T>G (p.Asn1233Lys)
Xg.74740858A>GCA517466455NEXMIFc.3699T>C (p.Asn1233=)
dbSNP gnomAD v4
Xg.74740858A>TCA413664944NEXMIFc.3699T>A (p.Asn1233Lys)
Xg.74740859T>ACA413664945NEXMIFc.3698A>T (p.Asn1233Ile)
Xg.74740859T>CCA413664946NEXMIFc.3698A>G (p.Asn1233Ser)
Xg.74740859T>GCA413664947NEXMIFc.3698A>C (p.Asn1233Thr)
Xg.74740860T>ACA413664948NEXMIFc.3697A>T (p.Asn1233Tyr)
Xg.74740860T>CCA413664949NEXMIFc.3697A>G (p.Asn1233Asp)
Xg.74740860T>GCA413664950NEXMIFc.3697A>C (p.Asn1233His)
Xg.74740861G>ACA517466457NEXMIFc.3696C>T (p.Ile1232=)
dbSNP
Xg.74740861G>CCA413664951NEXMIFc.3696C>G (p.Ile1232Met)
Xg.74740861G=CA2437590145NEXMIFc.3696C= (p.Ile1232=)
Xg.74740861G>TCA517466459NEXMIFc.3696C>A (p.Ile1232=)
Xg.74740862A>CCA413664952NEXMIFc.3695T>G (p.Ile1232Ser)
Xg.74740862A>GCA413664953NEXMIFc.3695T>C (p.Ile1232Thr)
Xg.74740862A>TCA413664954NEXMIFc.3695T>A (p.Ile1232Asn)
Xg.74740863T>ACA413664956NEXMIFc.3694A>T (p.Ile1232Phe)
Xg.74740863T>CCA331301709NEXMIFc.3694A>G (p.Ile1232Val)
dbSNP gnomAD v3 gnomAD v4
Xg.74740863T>GCA413664955NEXMIFc.3694A>C (p.Ile1232Leu)
Xg.74740863T=CA2437590146NEXMIFc.3694A= (p.Ile1232=)
Xg.74740864G>ACA517466466NEXMIFc.3693C>T (p.Ala1231=)
dbSNP gnomAD v3 gnomAD v4
Xg.74740864G>CCA517466465NEXMIFc.3693C>G (p.Ala1231=)
Xg.74740864G=CA2437590147NEXMIFc.3693C= (p.Ala1231=)
Xg.74740864G>TCA517466463NEXMIFc.3693C>A (p.Ala1231=)
Xg.74740865G>ACA413664957NEXMIFc.3692C>T (p.Ala1231Val)
Xg.74740865G>CCA413664958NEXMIFc.3692C>G (p.Ala1231Gly)
Xg.74740865G>TCA413664959NEXMIFc.3692C>A (p.Ala1231Asp)
Xg.74740866C>ACA413664960NEXMIFc.3691G>T (p.Ala1231Ser)
ClinVar dbSNP gnomAD v4
Xg.74740866C=CA2437590148NEXMIFc.3691G= (p.Ala1231=)
Xg.74740866C>GCA413664961NEXMIFc.3691G>C (p.Ala1231Pro)
Xg.74740866C>TCA413664962NEXMIFc.3691G>A (p.Ala1231Thr)
Xg.74740867A>CCA517466471NEXMIFc.3690T>G (p.Ala1230=)
Xg.74740867A>GCA517466473NEXMIFc.3690T>C (p.Ala1230=)
Xg.74740867A>TCA517466474NEXMIFc.3690T>A (p.Ala1230=)
Xg.74740867_74740868delinsAGCA2437590149NEXMIFc.3689_3690delinsCT (p.Ala1230=)
Xg.74740868delCA915951283NEXMIFc.3689del (p.Ala1230ValfsTer?)
ClinVar dbSNP
Xg.74740868G>ACA413664963NEXMIFc.3689C>T (p.Ala1230Val)
gnomAD v4
Xg.74740868G>CCA413664964NEXMIFc.3689C>G (p.Ala1230Gly)
Xg.74740868G>TCA413664965NEXMIFc.3689C>A (p.Ala1230Asp)
Xg.74740869C>ACA413664966NEXMIFc.3688G>T (p.Ala1230Ser)
Xg.74740869C>GCA413664967NEXMIFc.3688G>C (p.Ala1230Pro)
gnomAD v4
Xg.74740869C>TCA413664968NEXMIFc.3688G>A (p.Ala1230Thr)
gnomAD v4
Xg.74740870C>ACA413664970NEXMIFc.3687G>T (p.Met1229Ile)
COSMIC
Xg.74740870C>GCA413664971NEXMIFc.3687G>C (p.Met1229Ile)
Xg.74740870C>TCA413664969NEXMIFc.3687G>A (p.Met1229Ile)
Xg.74740871A=CA2437590150NEXMIFc.3686T= (p.Met1229=)
Xg.74740871A>CCA413664972NEXMIFc.3686T>G (p.Met1229Arg)
dbSNP gnomAD v4
Xg.74740871A>GCA413664973NEXMIFc.3686T>C (p.Met1229Thr)
Xg.74740871A>TCA413664974NEXMIFc.3686T>A (p.Met1229Lys)
Xg.74740872T>ACA413664975NEXMIFc.3685A>T (p.Met1229Leu)
Xg.74740872T>CCA413664976NEXMIFc.3685A>G (p.Met1229Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.74740872T>GCA413664977NEXMIFc.3685A>C (p.Met1229Leu)
Xg.74740872T=CA2437590151NEXMIFc.3685A= (p.Met1229=)
Xg.74740873G>ACA517466481NEXMIFc.3684C>T (p.Tyr1228=)
dbSNP gnomAD v3 gnomAD v4
Xg.74740873G>CCA413664978NEXMIFc.3684C>G (p.Tyr1228Ter)
Xg.74740873G=CA2437590152NEXMIFc.3684C= (p.Tyr1228=)
Xg.74740873G>TCA413664979NEXMIFc.3684C>A (p.Tyr1228Ter)
Xg.74740874T>ACA413664980NEXMIFc.3683A>T (p.Tyr1228Phe)
Xg.74740874T>CCA413664981NEXMIFc.3683A>G (p.Tyr1228Cys)
Xg.74740874T>GCA413664982NEXMIFc.3683A>C (p.Tyr1228Ser)
Xg.74740875A=CA2437590153NEXMIFc.3682T= (p.Tyr1228=)
Xg.74740875A>CCA413664983NEXMIFc.3682T>G (p.Tyr1228Asp)
Xg.74740875A>GCA413664984NEXMIFc.3682T>C (p.Tyr1228His)
ClinVar dbSNP gnomAD v4
Xg.74740875A>TCA413664985NEXMIFc.3682T>A (p.Tyr1228Asn)
Xg.74740876T>ACA413664986NEXMIFc.3681A>T (p.Lys1227Asn)
Xg.74740876T>CCA517466486NEXMIFc.3681A>G (p.Lys1227=)
Xg.74740876T>GCA413664987NEXMIFc.3681A>C (p.Lys1227Asn)
Xg.74740877T>ACA413664988NEXMIFc.3680A>T (p.Lys1227Ile)
Xg.74740877T>CCA413664989NEXMIFc.3680A>G (p.Lys1227Arg)
Xg.74740877T>GCA413664990NEXMIFc.3680A>C (p.Lys1227Thr)
Xg.74740878T>ACA413664991NEXMIFc.3679A>T (p.Lys1227Ter)
Xg.74740878T>CCA413664992NEXMIFc.3679A>G (p.Lys1227Glu)
Xg.74740878T>GCA413664993NEXMIFc.3679A>C (p.Lys1227Gln)
dbSNP
Xg.74740878T=CA2437590154NEXMIFc.3679A= (p.Lys1227=)
Xg.74740879C>ACA331301710NEXMIFc.3678G>T (p.Gly1226=)
dbSNP gnomAD v4
Xg.74740879C=CA2437590155NEXMIFc.3678G= (p.Gly1226=)
Xg.74740879C>GCA517466495NEXMIFc.3678G>C (p.Gly1226=)
Xg.74740879C>TCA517466497NEXMIFc.3678G>A (p.Gly1226=)
ClinVar dbSNP gnomAD v4
Xg.74740880C>ACA413664994NEXMIFc.3677G>T (p.Gly1226Val)
Xg.74740880C=CA2437590156NEXMIFc.3677G= (p.Gly1226=)
Xg.74740880C>GCA413664995NEXMIFc.3677G>C (p.Gly1226Ala)
gnomAD v4
Xg.74740880C>TCA10454920NEXMIFc.3677G>A (p.Gly1226Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74740881C>ACA413664996NEXMIFc.3676G>T (p.Gly1226Trp)
Xg.74740881C>GCA413664997NEXMIFc.3676G>C (p.Gly1226Arg)
Xg.74740881C>TCA413664998NEXMIFc.3676G>A (p.Gly1226Arg)
Xg.74740882T>ACA413664999NEXMIFc.3675A>T (p.Lys1225Asn)
gnomAD v4
Xg.74740882T>CCA517466508NEXMIFc.3675A>G (p.Lys1225=)
Xg.74740882T>GCA413665000NEXMIFc.3675A>C (p.Lys1225Asn)
Xg.74740883T>ACA413665001NEXMIFc.3674A>T (p.Lys1225Ile)
Xg.74740883T>CCA413665003NEXMIFc.3674A>G (p.Lys1225Arg)
Xg.74740883T>GCA413665002NEXMIFc.3674A>C (p.Lys1225Thr)
Xg.74740884T>ACA413665004NEXMIFc.3673A>T (p.Lys1225Ter)
Xg.74740884T>CCA413665005NEXMIFc.3673A>G (p.Lys1225Glu)
Xg.74740884T>GCA413665006NEXMIFc.3673A>C (p.Lys1225Gln)
Xg.74740885C>ACA413665007NEXMIFc.3672G>T (p.Lys1224Asn)
Xg.74740885C>GCA413665008NEXMIFc.3672G>C (p.Lys1224Asn)
Xg.74740885C>TCA517466514NEXMIFc.3672G>A (p.Lys1224=)
Xg.74740886T>ACA413665009NEXMIFc.3671A>T (p.Lys1224Met)
Xg.74740886T>CCA413665010NEXMIFc.3671A>G (p.Lys1224Arg)
Xg.74740886T>GCA413665011NEXMIFc.3671A>C (p.Lys1224Thr)
Xg.74740887T>ACA413665012NEXMIFc.3670A>T (p.Lys1224Ter)
Xg.74740887T>CCA413665013NEXMIFc.3670A>G (p.Lys1224Glu)
gnomAD v4
Xg.74740887T>GCA413665014NEXMIFc.3670A>C (p.Lys1224Gln)
Xg.74740888T>ACA517466518NEXMIFc.3669A>T (p.Thr1223=)
Xg.74740888T>CCA517466519NEXMIFc.3669A>G (p.Thr1223=)
Xg.74740888T>GCA517466520NEXMIFc.3669A>C (p.Thr1223=)
Xg.74740889G>ACA413665017NEXMIFc.3668C>T (p.Thr1223Ile)
Xg.74740889G>CCA413665015NEXMIFc.3668C>G (p.Thr1223Arg)
Xg.74740889G=CA2437590157NEXMIFc.3668C= (p.Thr1223=)
Xg.74740889G>TCA413665016NEXMIFc.3668C>A (p.Thr1223Lys)
dbSNP
Xg.74740890T>ACA413665018NEXMIFc.3667A>T (p.Thr1223Ser)
Xg.74740890T>CCA413665019NEXMIFc.3667A>G (p.Thr1223Ala)
Xg.74740890T>GCA413665020NEXMIFc.3667A>C (p.Thr1223Pro)
Xg.74740891G>ACA517466522NEXMIFc.3666C>T (p.Ser1222=)
Xg.74740891G>CCA517466523NEXMIFc.3666C>G (p.Ser1222=)
Xg.74740891G>TCA517466525NEXMIFc.3666C>A (p.Ser1222=)
Xg.74740892G>ACA413665021NEXMIFc.3665C>T (p.Ser1222Phe)
Xg.74740892G>CCA413665022NEXMIFc.3665C>G (p.Ser1222Cys)
Xg.74740892G>TCA413665023NEXMIFc.3665C>A (p.Ser1222Tyr)
Xg.74740893A>CCA413665024NEXMIFc.3664T>G (p.Ser1222Ala)
Xg.74740893A>GCA413665025NEXMIFc.3664T>C (p.Ser1222Pro)
Xg.74740893A>TCA413665026NEXMIFc.3664T>A (p.Ser1222Thr)
Xg.74740894C>ACA413665027NEXMIFc.3663G>T (p.Lys1221Asn)
Xg.74740894C>GCA413665028NEXMIFc.3663G>C (p.Lys1221Asn)
Xg.74740894C>TCA517466530NEXMIFc.3663G>A (p.Lys1221=)
Xg.74740895T>ACA413665030NEXMIFc.3662A>T (p.Lys1221Met)
Xg.74740895T>CCA413665031NEXMIFc.3662A>G (p.Lys1221Arg)
Xg.74740895T>GCA413665029NEXMIFc.3662A>C (p.Lys1221Thr)
dbSNP gnomAD v3 gnomAD v4
Xg.74740895T=CA2437590158NEXMIFc.3662A= (p.Lys1221=)
Xg.74740896T>ACA413665032NEXMIFc.3661A>T (p.Lys1221Ter)
Xg.74740896T>CCA413665033NEXMIFc.3661A>G (p.Lys1221Glu)
Xg.74740896T>GCA413665034NEXMIFc.3661A>C (p.Lys1221Gln)
Xg.74740897A=CA2437590159NEXMIFc.3660T= (p.Pro1220=)
Xg.74740897A>CCA517466534NEXMIFc.3660T>G (p.Pro1220=)
Xg.74740897A>GCA517466536NEXMIFc.3660T>C (p.Pro1220=)
dbSNP
Xg.74740897A>TCA517466535NEXMIFc.3660T>A (p.Pro1220=)
Xg.74740898G>ACA413665035NEXMIFc.3659C>T (p.Pro1220Leu)
gnomAD v4 COSMIC
Xg.74740898G>CCA413665036NEXMIFc.3659C>G (p.Pro1220Arg)
Xg.74740898G>TCA413665037NEXMIFc.3659C>A (p.Pro1220His)
Xg.74740899G>ACA413665038NEXMIFc.3658C>T (p.Pro1220Ser)
Xg.74740899G>CCA413665039NEXMIFc.3658C>G (p.Pro1220Ala)
Xg.74740899G=CA2437590160NEXMIFc.3658C= (p.Pro1220=)
Xg.74740899G>TCA413665041NEXMIFc.3658C>A (p.Pro1220Thr)
dbSNP
Xg.74740900G>ACA517466537NEXMIFc.3657C>T (p.Val1219=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.74740900G>CCA517466538NEXMIFc.3657C>G (p.Val1219=)
gnomAD v4
Xg.74740900G=CA2437590161NEXMIFc.3657C= (p.Val1219=)
Xg.74740900G>TCA517466539NEXMIFc.3657C>A (p.Val1219=)
Xg.74740901A=CA2437590162NEXMIFc.3656T= (p.Val1219=)
Xg.74740901A>CCA331301711NEXMIFc.3656T>G (p.Val1219Gly)
dbSNP gnomAD v4
Xg.74740901A>GCA413665043NEXMIFc.3656T>C (p.Val1219Ala)
dbSNP gnomAD v3 gnomAD v4
Xg.74740901A>TCA413665045NEXMIFc.3656T>A (p.Val1219Asp)
Xg.74740902C>ACA413665049NEXMIFc.3655G>T (p.Val1219Phe)
Xg.74740902C>GCA413665051NEXMIFc.3655G>C (p.Val1219Leu)
Xg.74740902C>TCA413665047NEXMIFc.3655G>A (p.Val1219Ile)
ClinVar
Xg.74740903C>ACA413665055NEXMIFc.3654G>T (p.Gln1218His)
Xg.74740903C>GCA413665056NEXMIFc.3654G>C (p.Gln1218His)
gnomAD v4
Xg.74740903C>TCA517466546NEXMIFc.3654G>A (p.Gln1218=)
gnomAD v4
Xg.74740904T>ACA413665057NEXMIFc.3653A>T (p.Gln1218Leu)
Xg.74740904T>CCA331301712NEXMIFc.3653A>G (p.Gln1218Arg)
ClinVar dbSNP
Xg.74740904T>GCA413665059NEXMIFc.3653A>C (p.Gln1218Pro)
Xg.74740904T=CA2437590163NEXMIFc.3653A= (p.Gln1218=)
Xg.74740905G>ACA413665065NEXMIFc.3652C>T (p.Gln1218Ter)
COSMIC
Xg.74740905G>CCA413665063NEXMIFc.3652C>G (p.Gln1218Glu)
Xg.74740905G>TCA413665062NEXMIFc.3652C>A (p.Gln1218Lys)
Xg.74740906G>ACA517466550NEXMIFc.3651C>T (p.Arg1217=)
Xg.74740906G>CCA517466551NEXMIFc.3651C>G (p.Arg1217=)
Xg.74740906G>TCA517466552NEXMIFc.3651C>A (p.Arg1217=)
Xg.74740907C>ACA413665067NEXMIFc.3650G>T (p.Arg1217Leu)
dbSNP
Xg.74740907C=CA2437590164NEXMIFc.3650G= (p.Arg1217=)
Xg.74740907C>GCA413665069NEXMIFc.3650G>C (p.Arg1217Pro)
Xg.74740907C>TCA10454921NEXMIFc.3650G>A (p.Arg1217His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
Xg.74740908G>ACA331301713NEXMIFc.3649C>T (p.Arg1217Cys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
Xg.74740908G>CCA413665072NEXMIFc.3649C>G (p.Arg1217Gly)
Xg.74740908G=CA2437590165NEXMIFc.3649C= (p.Arg1217=)
Xg.74740908G>TCA413665074NEXMIFc.3649C>A (p.Arg1217Ser)
Xg.74740909G>ACA10454922NEXMIFc.3648C>T (p.Ser1216=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74740909G>CCA517466557NEXMIFc.3648C>G (p.Ser1216=)
Xg.74740909G=CA2437590166NEXMIFc.3648C= (p.Ser1216=)
Xg.74740909G>TCA517466558NEXMIFc.3648C>A (p.Ser1216=)
Xg.74740910G>ACA413665080NEXMIFc.3647C>T (p.Ser1216Phe)
Xg.74740910G>CCA413665079NEXMIFc.3647C>G (p.Ser1216Cys)
Xg.74740910G>TCA413665077NEXMIFc.3647C>A (p.Ser1216Tyr)
Xg.74740911A>CCA413665084NEXMIFc.3646T>G (p.Ser1216Ala)
Xg.74740911A>GCA413665082NEXMIFc.3646T>C (p.Ser1216Pro)
Xg.74740911A>TCA413665086NEXMIFc.3646T>A (p.Ser1216Thr)
Xg.74740912G>ACA517466562NEXMIFc.3645C>T (p.Asn1215=)
Xg.74740912G>CCA413665088NEXMIFc.3645C>G (p.Asn1215Lys)
Xg.74740912G>TCA413665090NEXMIFc.3645C>A (p.Asn1215Lys)
Xg.74740913T>ACA413665092NEXMIFc.3644A>T (p.Asn1215Ile)
Xg.74740913T>CCA413665094NEXMIFc.3644A>G (p.Asn1215Ser)
Xg.74740913T>GCA331301714NEXMIFc.3644A>C (p.Asn1215Thr)
dbSNP
Xg.74740913T=CA2437590167NEXMIFc.3644A= (p.Asn1215=)
Xg.74740914T>ACA413665096NEXMIFc.3643A>T (p.Asn1215Tyr)
Xg.74740914T>CCA413665099NEXMIFc.3643A>G (p.Asn1215Asp)
Xg.74740914T>GCA413665098NEXMIFc.3643A>C (p.Asn1215His)
Xg.74740915T>ACA413665101NEXMIFc.3642A>T (p.Lys1214Asn)
Xg.74740915T>CCA517466565NEXMIFc.3642A>G (p.Lys1214=)
Xg.74740915T>GCA413665104NEXMIFc.3642A>C (p.Lys1214Asn)
Xg.74740916T>ACA413665106NEXMIFc.3641A>T (p.Lys1214Ile)
Xg.74740916T>CCA413665107NEXMIFc.3641A>G (p.Lys1214Arg)
ClinVar
Xg.74740916T>GCA413665109NEXMIFc.3641A>C (p.Lys1214Thr)
Xg.74740917T>ACA413665111NEXMIFc.3640A>T (p.Lys1214Ter)
Xg.74740917T>CCA413665113NEXMIFc.3640A>G (p.Lys1214Glu)
Xg.74740917T>GCA413665114NEXMIFc.3640A>C (p.Lys1214Gln)
Xg.74740918G>ACA517466572NEXMIFc.3639C>T (p.Gly1213=)
gnomAD v4
Xg.74740918G>CCA517466570NEXMIFc.3639C>G (p.Gly1213=)
ClinVar
Xg.74740918G>TCA517466571NEXMIFc.3639C>A (p.Gly1213=)
Xg.74740919C>ACA413665117NEXMIFc.3638G>T (p.Gly1213Val)
Xg.74740919C=CA2437590168NEXMIFc.3638G= (p.Gly1213=)
Xg.74740919C>GCA413665118NEXMIFc.3638G>C (p.Gly1213Ala)
Xg.74740919C>TCA413665120NEXMIFc.3638G>A (p.Gly1213Asp)
ClinVar dbSNP
Xg.74740920C>ACA413665122NEXMIFc.3637G>T (p.Gly1213Cys)
Xg.74740920C=CA2437590169NEXMIFc.3637G= (p.Gly1213=)
Xg.74740920C>GCA413665124NEXMIFc.3637G>C (p.Gly1213Arg)
Xg.74740920C>TCA205233NEXMIFc.3637G>A (p.Gly1213Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.74740921A>CCA517466576NEXMIFc.3636T>G (p.Pro1212=)
Xg.74740921A>GCA517466577NEXMIFc.3636T>C (p.Pro1212=)
Xg.74740921A>TCA517466579NEXMIFc.3636T>A (p.Pro1212=)
Xg.74740922G>ACA413665126NEXMIFc.3635C>T (p.Pro1212Leu)
Xg.74740922G>CCA413665128NEXMIFc.3635C>G (p.Pro1212Arg)
Xg.74740922G>TCA413665129NEXMIFc.3635C>A (p.Pro1212His)
Xg.74740923G>ACA413665132NEXMIFc.3634C>T (p.Pro1212Ser)
dbSNP
Xg.74740923G>CCA413665133NEXMIFc.3634C>G (p.Pro1212Ala)
COSMIC
Xg.74740923G=CA2437590170NEXMIFc.3634C= (p.Pro1212=)
Xg.74740923G>TCA413665135NEXMIFc.3634C>A (p.Pro1212Thr)
Xg.74740924T>ACA517466581NEXMIFc.3633A>T (p.Pro1211=)
Xg.74740924T>CCA517466582NEXMIFc.3633A>G (p.Pro1211=)
ClinVar dbSNP gnomAD v4
Xg.74740924T>GCA517466583NEXMIFc.3633A>C (p.Pro1211=)
Xg.74740924T=CA2437590171NEXMIFc.3633A= (p.Pro1211=)
Xg.74740925G>ACA413665136NEXMIFc.3632C>T (p.Pro1211Leu)
Xg.74740925G>CCA413665137NEXMIFc.3632C>G (p.Pro1211Arg)
Xg.74740925G>TCA413665139NEXMIFc.3632C>A (p.Pro1211Gln)
Xg.74740926G>ACA331301715NEXMIFc.3631C>T (p.Pro1211Ser)
dbSNP gnomAD v4 COSMIC
Xg.74740926G>CCA413665143NEXMIFc.3631C>G (p.Pro1211Ala)
Xg.74740926G=CA2437590173NEXMIFc.3631C= (p.Pro1211=)
Xg.74740926G>TCA413665141NEXMIFc.3631C>A (p.Pro1211Thr)
gnomAD v4
Xg.74740926_74740929delinsGTTTCA2437590172NEXMIFc.3628_3631delinsAAAC (p.Lys1210=)
Xg.74740927T>ACA413665145NEXMIFc.3630A>T (p.Lys1210Asn)
Xg.74740927T>CCA331301716NEXMIFc.3630A>G (p.Lys1210=)
dbSNP gnomAD v4
Xg.74740927T>GCA413665148NEXMIFc.3630A>C (p.Lys1210Asn)
Xg.74740927T=CA2437590174NEXMIFc.3630A= (p.Lys1210=)
Xg.74740931delCA1139667659NEXMIFc.3630del (p.Lys1210AsnfsTer?)
ClinVar dbSNP
Xg.74740929_74740931delCA10454923NEXMIFc.3628_3630del (p.Lys1210del)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74740928T>ACA413665150NEXMIFc.3629A>T (p.Lys1210Ile)
Xg.74740928T>CCA413665152NEXMIFc.3629A>G (p.Lys1210Arg)
Xg.74740928T>GCA413665154NEXMIFc.3629A>C (p.Lys1210Thr)
Xg.74740929T>ACA413665155NEXMIFc.3628A>T (p.Lys1210Ter)
Xg.74740929T>CCA413665157NEXMIFc.3628A>G (p.Lys1210Glu)
Xg.74740929T>GCA413665159NEXMIFc.3628A>C (p.Lys1210Gln)
Xg.74740930T>ACA413665161NEXMIFc.3627A>T (p.Glu1209Asp)
Xg.74740930T>CCA517466589NEXMIFc.3627A>G (p.Glu1209=)
Xg.74740930T>GCA413665162NEXMIFc.3627A>C (p.Glu1209Asp)
Xg.74740931T>ACA413665170NEXMIFc.3626A>T (p.Glu1209Val)
Xg.74740931T>CCA413665164NEXMIFc.3626A>G (p.Glu1209Gly)
Xg.74740931T>GCA413665166NEXMIFc.3626A>C (p.Glu1209Ala)
Xg.74740932C>ACA413665172NEXMIFc.3625G>T (p.Glu1209Ter)
Xg.74740932C>GCA413665173NEXMIFc.3625G>C (p.Glu1209Gln)
Xg.74740932C>TCA413665175NEXMIFc.3625G>A (p.Glu1209Lys)
Xg.74740933A>CCA413665177NEXMIFc.3624T>G (p.Ile1208Met)
Xg.74740933A>GCA517466594NEXMIFc.3624T>C (p.Ile1208=)
Xg.74740933A>TCA517466595NEXMIFc.3624T>A (p.Ile1208=)
Xg.74740934A>CCA413665179NEXMIFc.3623T>G (p.Ile1208Ser)
Xg.74740934A>GCA413665181NEXMIFc.3623T>C (p.Ile1208Thr)
Xg.74740934A>TCA413665182NEXMIFc.3623T>A (p.Ile1208Asn)
gnomAD v4
Xg.74740935T>ACA413665184NEXMIFc.3622A>T (p.Ile1208Phe)
Xg.74740935T>CCA413665186NEXMIFc.3622A>G (p.Ile1208Val)
gnomAD v4
Xg.74740935T>GCA413665188NEXMIFc.3622A>C (p.Ile1208Leu)
dbSNP gnomAD v3 gnomAD v4
Xg.74740935T=CA2437590175NEXMIFc.3622A= (p.Ile1208=)
Xg.74740936C>ACA517466600NEXMIFc.3621G>T (p.Gly1207=)
gnomAD v4
Xg.74740936C>GCA517466601NEXMIFc.3621G>C (p.Gly1207=)
Xg.74740936C>TCA517466602NEXMIFc.3621G>A (p.Gly1207=)
COSMIC
Xg.74740937C>ACA413665190NEXMIFc.3620G>T (p.Gly1207Val)
Xg.74740937C=CA2437590176NEXMIFc.3620G= (p.Gly1207=)
Xg.74740937C>GCA413665192NEXMIFc.3620G>C (p.Gly1207Ala)
Xg.74740937C>TCA331301717NEXMIFc.3620G>A (p.Gly1207Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.74740938C>ACA413665197NEXMIFc.3619G>T (p.Gly1207Trp)
Xg.74740938C>GCA413665198NEXMIFc.3619G>C (p.Gly1207Arg)
Xg.74740938C>TCA413665195NEXMIFc.3619G>A (p.Gly1207Arg)
Xg.74740939C>ACA413665201NEXMIFc.3618G>T (p.Lys1206Asn)
Xg.74740939C>GCA413665200NEXMIFc.3618G>C (p.Lys1206Asn)
Xg.74740939C>TCA517466609NEXMIFc.3618G>A (p.Lys1206=)
Xg.74740939_74740942delinsCTTGCA2437590177NEXMIFc.3615_3618delinsCAAG (p.Asn1205=)
Xg.74740940T>ACA413665204NEXMIFc.3617A>T (p.Lys1206Met)
Xg.74740940T>CCA413665205NEXMIFc.3617A>G (p.Lys1206Arg)
Xg.74740940T>GCA413665207NEXMIFc.3617A>C (p.Lys1206Thr)
Xg.74740945_74740947delCA10454924NEXMIFc.3615_3617del (p.Asn1205del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74740941T>ACA413665208NEXMIFc.3616A>T (p.Lys1206Ter)
Xg.74740941T>CCA413665210NEXMIFc.3616A>G (p.Lys1206Glu)
Xg.74740941T>GCA413665212NEXMIFc.3616A>C (p.Lys1206Gln)
Xg.74740942G>ACA517466611NEXMIFc.3615C>T (p.Asn1205=)
dbSNP gnomAD v4
Xg.74740942G>CCA413665214NEXMIFc.3615C>G (p.Asn1205Lys)
Xg.74740942G=CA2437590178NEXMIFc.3615C= (p.Asn1205=)
Xg.74740942G>TCA413665215NEXMIFc.3615C>A (p.Asn1205Lys)
gnomAD v4
Xg.74740943T>ACA413665217NEXMIFc.3614A>T (p.Asn1205Ile)
Xg.74740943T>CCA413665219NEXMIFc.3614A>G (p.Asn1205Ser)
Xg.74740943T>GCA413665220NEXMIFc.3614A>C (p.Asn1205Thr)
Xg.74740944T>ACA413665226NEXMIFc.3613A>T (p.Asn1205Tyr)
Xg.74740944T>CCA413665222NEXMIFc.3613A>G (p.Asn1205Asp)
Xg.74740944T>GCA413665225NEXMIFc.3613A>C (p.Asn1205His)
Xg.74740945G>ACA10454925NEXMIFc.3612C>T (p.Asn1204=)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74740945G>CCA413665227NEXMIFc.3612C>G (p.Asn1204Lys)
ClinVar
Xg.74740945G=CA2437590179NEXMIFc.3612C= (p.Asn1204=)
Xg.74740945G>TCA413665228NEXMIFc.3612C>A (p.Asn1204Lys)
COSMIC
Xg.74740945_74740962delinsGTTACCTTTGAGGGATTTCA2437590180NEXMIFc.3595_3612delinsAAATCCCTCAAAGGTAAC (p.Lys1199=)
Xg.74740946T>ACA413665229NEXMIFc.3611A>T (p.Asn1204Ile)
gnomAD v4
Xg.74740946T>CCA413665230NEXMIFc.3611A>G (p.Asn1204Ser)
Xg.74740946T>GCA413665231NEXMIFc.3611A>C (p.Asn1204Thr)
Xg.74740948_74740964delCA658659014NEXMIFc.3595_3611del (p.Lys1199GlnfsTer5)
ClinVar dbSNP
Xg.74740947T>ACA413665232NEXMIFc.3610A>T (p.Asn1204Tyr)
Xg.74740947T>CCA413665233NEXMIFc.3610A>G (p.Asn1204Asp)
Xg.74740947T>GCA413665234NEXMIFc.3610A>C (p.Asn1204His)
Xg.74740948A>CCA517466082NEXMIFc.3609T>G (p.Gly1203=)
Xg.74740948A>GCA517466085NEXMIFc.3609T>C (p.Gly1203=)
Xg.74740948A>TCA517466083NEXMIFc.3609T>A (p.Gly1203=)
Xg.74740949C>ACA413665236NEXMIFc.3608G>T (p.Gly1203Val)
dbSNP
Xg.74740949C=CA2437590181NEXMIFc.3608G= (p.Gly1203=)
Xg.74740949C>GCA413665238NEXMIFc.3608G>C (p.Gly1203Ala)
Xg.74740949C>TCA413665240NEXMIFc.3608G>A (p.Gly1203Asp)
Xg.74740950C>ACA413665245NEXMIFc.3607G>T (p.Gly1203Cys)
Xg.74740950C>GCA413665243NEXMIFc.3607G>C (p.Gly1203Arg)
gnomAD v4
Xg.74740950C>TCA413665242NEXMIFc.3607G>A (p.Gly1203Ser)
gnomAD v4
Xg.74740951T>ACA413665247NEXMIFc.3606A>T (p.Lys1202Asn)
Xg.74740951T>CCA517466089NEXMIFc.3606A>G (p.Lys1202=)
dbSNP
Xg.74740951T>GCA413665249NEXMIFc.3606A>C (p.Lys1202Asn)
Xg.74740951T=CA2437590182NEXMIFc.3606A= (p.Lys1202=)
Xg.74740952T>ACA413665251NEXMIFc.3605A>T (p.Lys1202Ile)
Xg.74740952T>CCA413665253NEXMIFc.3605A>G (p.Lys1202Arg)
Xg.74740952T>GCA413665256NEXMIFc.3605A>C (p.Lys1202Thr)
Xg.74740953T>ACA413665262NEXMIFc.3604A>T (p.Lys1202Ter)
Xg.74740953T>CCA413665260NEXMIFc.3604A>G (p.Lys1202Glu)
Xg.74740953T>GCA413665258NEXMIFc.3604A>C (p.Lys1202Gln)
Xg.74740954G>ACA517466097NEXMIFc.3603C>T (p.Leu1201=)
Xg.74740954G>CCA517466098NEXMIFc.3603C>G (p.Leu1201=)
Xg.74740954G>TCA517466099NEXMIFc.3603C>A (p.Leu1201=)
Xg.74740955A=CA2437590183NEXMIFc.3602T= (p.Leu1201=)
Xg.74740955A>CCA413665264NEXMIFc.3602T>G (p.Leu1201Arg)
Xg.74740955A>GCA413665265NEXMIFc.3602T>C (p.Leu1201Pro)
Xg.74740955A>TCA413665266NEXMIFc.3602T>A (p.Leu1201His)
dbSNP gnomAD v2 gnomAD v4
Xg.74740956G>ACA413665269NEXMIFc.3601C>T (p.Leu1201Phe)
ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.74740956G>CCA413665270NEXMIFc.3601C>G (p.Leu1201Val)
Xg.74740956G=CA2437590184NEXMIFc.3601C= (p.Leu1201=)
Xg.74740956G>TCA413665272NEXMIFc.3601C>A (p.Leu1201Ile)
gnomAD v4

Number of alleles fetched