Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.74740945_74740962delinsGTTACCTTTGAGGGATTTCA2437590180NEXMIFc.3595_3612delinsAAATCCCTCAAAGGTAAC (p.Lys1199=)
Xg.74740948_74740964delCA658659014NEXMIFc.3595_3611del (p.Lys1199GlnfsTer5)
ClinVar dbSNP
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
Xg.74740957G>ACA517466101NEXMIFc.3600C>T (p.Ser1200=)
ClinVar COSMIC
Xg.74740957G>CCA517466102NEXMIFc.3600C>G (p.Ser1200=)
Xg.74740957G>TCA517466103NEXMIFc.3600C>A (p.Ser1200=)
Xg.74740958G>ACA413665274NEXMIFc.3599C>T (p.Ser1200Phe)
COSMIC
Xg.74740958G>CCA413665277NEXMIFc.3599C>G (p.Ser1200Cys)
Xg.74740958G>TCA413665276NEXMIFc.3599C>A (p.Ser1200Tyr)
Xg.74740958_74740959insTCA645603757NEXMIFc.3598_3599insA (p.Ser1200TyrfsTer5)
COSMIC
Xg.74740959A=CA2437590185NEXMIFc.3598T= (p.Ser1200=)
Xg.74740959A>CCA413665279NEXMIFc.3598T>G (p.Ser1200Ala)
Xg.74740959A>GCA413665281NEXMIFc.3598T>C (p.Ser1200Pro)
Xg.74740959A>TCA413665283NEXMIFc.3598T>A (p.Ser1200Thr)
Xg.74740960T>ACA413665286NEXMIFc.3597A>T (p.Lys1199Asn)
Xg.74740960T>CCA517466113NEXMIFc.3597A>G (p.Lys1199=)
dbSNP gnomAD v2 gnomAD v4
Xg.74740960T>GCA413665287NEXMIFc.3597A>C (p.Lys1199Asn)
Xg.74740960T=CA2437590186NEXMIFc.3597A= (p.Lys1199=)
Xg.74740965dupCA145333NEXMIFc.3597dup (p.Ser1200IlefsTer5)
ClinVar dbSNP
Xg.74740961T>ACA413665289NEXMIFc.3596A>T (p.Lys1199Ile)
Xg.74740961T>CCA413665290NEXMIFc.3596A>G (p.Lys1199Arg)
Xg.74740961T>GCA413665292NEXMIFc.3596A>C (p.Lys1199Thr)
Xg.74740962T>ACA413665293NEXMIFc.3595A>T (p.Lys1199Ter)
Xg.74740962T>CCA413665294NEXMIFc.3595A>G (p.Lys1199Glu)
Xg.74740962T>GCA413665296NEXMIFc.3595A>C (p.Lys1199Gln)
Xg.74740963T>ACA413665300NEXMIFc.3594A>T (p.Lys1198Asn)
Xg.74740963T>CCA517466118NEXMIFc.3594A>G (p.Lys1198=)
Xg.74740963T>GCA413665298NEXMIFc.3594A>C (p.Lys1198Asn)
Xg.74740964T>ACA10454926NEXMIFc.3593A>T (p.Lys1198Ile)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.74740964T>CCA413665305NEXMIFc.3593A>G (p.Lys1198Arg)
Xg.74740964T>GCA413665303NEXMIFc.3593A>C (p.Lys1198Thr)
Xg.74740964T=CA2437590187NEXMIFc.3593A= (p.Lys1198=)
Xg.74740965T>ACA413665307NEXMIFc.3592A>T (p.Lys1198Ter)
ClinVar dbSNP
Xg.74740965T>CCA413665311NEXMIFc.3592A>G (p.Lys1198Glu)
Xg.74740965T>GCA413665309NEXMIFc.3592A>C (p.Lys1198Gln)
Xg.74740966C>ACA413665313NEXMIFc.3591G>T (p.Arg1197Ser)
gnomAD v4
Xg.74740966C=CA2437590188NEXMIFc.3591G= (p.Arg1197=)
Xg.74740966C>GCA413665315NEXMIFc.3591G>C (p.Arg1197Ser)
Xg.74740966C>TCA10454927NEXMIFc.3591G>A (p.Arg1197=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
Xg.74740967delCA2695235568NEXMIFc.3591del (p.Lys1199AsnfsTer?)
Xg.74740967C>ACA413665317NEXMIFc.3590G>T (p.Arg1197Met)
COSMIC
Xg.74740967C>GCA413665319NEXMIFc.3590G>C (p.Arg1197Thr)
Xg.74740967C>TCA413665321NEXMIFc.3590G>A (p.Arg1197Lys)
dbSNP gnomAD v4 COSMIC
Xg.74740968T>ACA413665323NEXMIFc.3589A>T (p.Arg1197Trp)
Xg.74740968T>CCA413665324NEXMIFc.3589A>G (p.Arg1197Gly)
dbSNP gnomAD v2 gnomAD v4
Xg.74740968T>GCA517466119NEXMIFc.3589A>C (p.Arg1197=)
Xg.74740968T=CA2437590189NEXMIFc.3589A= (p.Arg1197=)
Xg.74740969G>ACA517466120NEXMIFc.3588C>T (p.Thr1196=)
Xg.74740969G>CCA517466121NEXMIFc.3588C>G (p.Thr1196=)
Xg.74740969G>TCA517466122NEXMIFc.3588C>A (p.Thr1196=)
Xg.74740970G>ACA413665326NEXMIFc.3587C>T (p.Thr1196Ile)
dbSNP gnomAD v4
Xg.74740970G>CCA413665328NEXMIFc.3587C>G (p.Thr1196Ser)
Xg.74740970G=CA2437590190NEXMIFc.3587C= (p.Thr1196=)
Xg.74740970G>TCA413665330NEXMIFc.3587C>A (p.Thr1196Asn)
Xg.74740971T>ACA413665335NEXMIFc.3586A>T (p.Thr1196Ser)
Xg.74740971T>CCA413665332NEXMIFc.3586A>G (p.Thr1196Ala)
ClinVar
Xg.74740971T>GCA413665334NEXMIFc.3586A>C (p.Thr1196Pro)
Xg.74740972G>ACA517466123NEXMIFc.3585C>T (p.Asn1195=)
Xg.74740972G>CCA413665337NEXMIFc.3585C>G (p.Asn1195Lys)
Xg.74740972G=CA2437590191NEXMIFc.3585C= (p.Asn1195=)
Xg.74740972G>TCA413665339NEXMIFc.3585C>A (p.Asn1195Lys)
Xg.74740973T>ACA413665340NEXMIFc.3584A>T (p.Asn1195Ile)
Xg.74740973T>CCA413665342NEXMIFc.3584A>G (p.Asn1195Ser)
Xg.74740973T>GCA413665344NEXMIFc.3584A>C (p.Asn1195Thr)
Xg.74740977dupCA915951284NEXMIFc.3584dup (p.Asn1195LysfsTer10)
ClinVar dbSNP
Xg.74740974T>ACA413665346NEXMIFc.3583A>T (p.Asn1195Tyr)
Xg.74740974T>CCA413665347NEXMIFc.3583A>G (p.Asn1195Asp)
Xg.74740974T>GCA413665349NEXMIFc.3583A>C (p.Asn1195His)
Xg.74740975T>ACA413665351NEXMIFc.3582A>T (p.Lys1194Asn)
Xg.74740975T>CCA517466125NEXMIFc.3582A>G (p.Lys1194=)
Xg.74740975T>GCA413665353NEXMIFc.3582A>C (p.Lys1194Asn)
Xg.74740976T>ACA413665356NEXMIFc.3581A>T (p.Lys1194Ile)
Xg.74740976T>CCA413665358NEXMIFc.3581A>G (p.Lys1194Arg)
Xg.74740976T>GCA413665354NEXMIFc.3581A>C (p.Lys1194Thr)
Xg.74740977T>ACA413665359NEXMIFc.3580A>T (p.Lys1194Ter)
Xg.74740977T>CCA413665361NEXMIFc.3580A>G (p.Lys1194Glu)
Xg.74740977T>GCA413665363NEXMIFc.3580A>C (p.Lys1194Gln)
Xg.74740978delCA2573055404NEXMIFc.3579del (p.Asn1195ThrfsTer?)
ClinVar dbSNP
Xg.74740978C>ACA413665365NEXMIFc.3579G>T (p.Gln1193His)
Xg.74740978C>GCA413665366NEXMIFc.3579G>C (p.Gln1193His)
Xg.74740978C>TCA517466127NEXMIFc.3579G>A (p.Gln1193=)
Xg.74740979T>ACA413665368NEXMIFc.3578A>T (p.Gln1193Leu)
ClinVar
Xg.74740979T>CCA413665370NEXMIFc.3578A>G (p.Gln1193Arg)
Xg.74740979T>GCA413665372NEXMIFc.3578A>C (p.Gln1193Pro)
Xg.74740980G>ACA413665373NEXMIFc.3577C>T (p.Gln1193Ter)
COSMIC
Xg.74740980G>CCA413665375NEXMIFc.3577C>G (p.Gln1193Glu)
Xg.74740980G>TCA413665377NEXMIFc.3577C>A (p.Gln1193Lys)
Xg.74740981A>CCA517466128NEXMIFc.3576T>G (p.Ser1192=)
Xg.74740981A>GCA517466129NEXMIFc.3576T>C (p.Ser1192=)
Xg.74740981A>TCA517466130NEXMIFc.3576T>A (p.Ser1192=)
Xg.74740982G>ACA413665380NEXMIFc.3575C>T (p.Ser1192Phe)
dbSNP gnomAD v3 gnomAD v4 COSMIC
Xg.74740982G>CCA413665382NEXMIFc.3575C>G (p.Ser1192Cys)
gnomAD v4
Xg.74740982G=CA2437590192NEXMIFc.3575C= (p.Ser1192=)
Xg.74740982G>TCA413665379NEXMIFc.3575C>A (p.Ser1192Tyr)
Xg.74740983A=CA2437590193NEXMIFc.3574T= (p.Ser1192=)
Xg.74740983A>CCA413665385NEXMIFc.3574T>G (p.Ser1192Ala)
Xg.74740983A>GCA413665386NEXMIFc.3574T>C (p.Ser1192Pro)
ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.74740983A>TCA413665388NEXMIFc.3574T>A (p.Ser1192Thr)
Xg.74740984A>CCA517466132NEXMIFc.3573T>G (p.Ser1191=)
Xg.74740984A>GCA517466133NEXMIFc.3573T>C (p.Ser1191=)
Xg.74740984A>TCA517466134NEXMIFc.3573T>A (p.Ser1191=)
Xg.74740985G>ACA413665389NEXMIFc.3572C>T (p.Ser1191Phe)
Xg.74740985G>CCA413665390NEXMIFc.3572C>G (p.Ser1191Cys)
Xg.74740985G>TCA413665392NEXMIFc.3572C>A (p.Ser1191Tyr)
Xg.74740986A=CA2437590194NEXMIFc.3571T= (p.Ser1191=)
Xg.74740986A>CCA10454929NEXMIFc.3571T>G (p.Ser1191Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74740986A>GCA10454928NEXMIFc.3571T>C (p.Ser1191Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74740986A>TCA413665394NEXMIFc.3571T>A (p.Ser1191Thr)
Xg.74740987G>ACA517466136NEXMIFc.3570C>T (p.Ser1190=)
Xg.74740987G>CCA413665395NEXMIFc.3570C>G (p.Ser1190Arg)
Xg.74740987G>TCA413665396NEXMIFc.3570C>A (p.Ser1190Arg)
Xg.74740988C>ACA413665397NEXMIFc.3569G>T (p.Ser1190Ile)
Xg.74740988C=CA2437590195NEXMIFc.3569G= (p.Ser1190=)
Xg.74740988C>GCA413665398NEXMIFc.3569G>C (p.Ser1190Thr)
Xg.74740988C>TCA10454930NEXMIFc.3569G>A (p.Ser1190Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74740989T>ACA413665401NEXMIFc.3568A>T (p.Ser1190Cys)
Xg.74740989T>CCA413665400NEXMIFc.3568A>G (p.Ser1190Gly)
Xg.74740989T>GCA413665399NEXMIFc.3568A>C (p.Ser1190Arg)
Xg.74740990T>ACA413665404NEXMIFc.3567A>T (p.Gln1189His)
Xg.74740990T>CCA517466139NEXMIFc.3567A>G (p.Gln1189=)
Xg.74740990T>GCA413665403NEXMIFc.3567A>C (p.Gln1189His)
Xg.74740991T>ACA413665408NEXMIFc.3566A>T (p.Gln1189Leu)
Xg.74740991T>CCA413665405NEXMIFc.3566A>G (p.Gln1189Arg)
dbSNP gnomAD v3 gnomAD v4
Xg.74740991T>GCA413665407NEXMIFc.3566A>C (p.Gln1189Pro)
Xg.74740991T=CA2437590196NEXMIFc.3566A= (p.Gln1189=)
Xg.74740991_74740992insTCTGAGAAGAGTGCA2695235569NEXMIFc.3565_3566insCACTCTTCTCAGA (p.Gln1189ProfsTer20)
Xg.74740992G>ACA413665410NEXMIFc.3565C>T (p.Gln1189Ter)
Xg.74740992G>CCA413665411NEXMIFc.3565C>G (p.Gln1189Glu)
Xg.74740992G>TCA413665413NEXMIFc.3565C>A (p.Gln1189Lys)
Xg.74740993G>ACA517466141NEXMIFc.3564C>T (p.Asn1188=)
Xg.74740993G>CCA413665415NEXMIFc.3564C>G (p.Asn1188Lys)
Xg.74740993G>TCA413665417NEXMIFc.3564C>A (p.Asn1188Lys)
Xg.74740994T>ACA413665419NEXMIFc.3563A>T (p.Asn1188Ile)
Xg.74740994T>CCA413665420NEXMIFc.3563A>G (p.Asn1188Ser)
Xg.74740994T>GCA413665421NEXMIFc.3563A>C (p.Asn1188Thr)
Xg.74740995T>ACA413665422NEXMIFc.3562A>T (p.Asn1188Tyr)
Xg.74740995T>CCA413665425NEXMIFc.3562A>G (p.Asn1188Asp)
Xg.74740995T>GCA413665427NEXMIFc.3562A>C (p.Asn1188His)
Xg.74740996C>ACA413665431NEXMIFc.3561G>T (p.Met1187Ile)
Xg.74740996C>GCA413665428NEXMIFc.3561G>C (p.Met1187Ile)
Xg.74740996C>TCA413665429NEXMIFc.3561G>A (p.Met1187Ile)
COSMIC
Xg.74740997A=CA2437590197NEXMIFc.3560T= (p.Met1187=)
Xg.74740997A>CCA413665434NEXMIFc.3560T>G (p.Met1187Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.74740997A>GCA413665435NEXMIFc.3560T>C (p.Met1187Thr)
gnomAD v4
Xg.74740997A>TCA413665436NEXMIFc.3560T>A (p.Met1187Lys)
Xg.74740998T>ACA413665437NEXMIFc.3559A>T (p.Met1187Leu)
Xg.74740998T>CCA10454931NEXMIFc.3559A>G (p.Met1187Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74740998T>GCA413665438NEXMIFc.3559A>C (p.Met1187Leu)
Xg.74740998T=CA2437590198NEXMIFc.3559A= (p.Met1187=)
Xg.74740999A>CCA517466143NEXMIFc.3558T>G (p.Ala1186=)
Xg.74740999A>GCA517466144NEXMIFc.3558T>C (p.Ala1186=)
Xg.74740999A>TCA517466145NEXMIFc.3558T>A (p.Ala1186=)
Xg.74741000G>ACA413665440NEXMIFc.3557C>T (p.Ala1186Val)
Xg.74741000G>CCA413665441NEXMIFc.3557C>G (p.Ala1186Gly)
Xg.74741000G>TCA413665443NEXMIFc.3557C>A (p.Ala1186Asp)
COSMIC
Xg.74741001C>ACA413665444NEXMIFc.3556G>T (p.Ala1186Ser)
Xg.74741001C>GCA413665446NEXMIFc.3556G>C (p.Ala1186Pro)
Xg.74741001C>TCA413665448NEXMIFc.3556G>A (p.Ala1186Thr)
Xg.74741002C>ACA10454932NEXMIFc.3555G>T (p.Gly1185=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.74741002C=CA2437590199NEXMIFc.3555G= (p.Gly1185=)
Xg.74741002C>GCA517466147NEXMIFc.3555G>C (p.Gly1185=)
Xg.74741002C>TCA517466148NEXMIFc.3555G>A (p.Gly1185=)
Xg.74741003C>ACA413665454NEXMIFc.3554G>T (p.Gly1185Val)
Xg.74741003C>GCA413665450NEXMIFc.3554G>C (p.Gly1185Ala)
Xg.74741003C>TCA413665452NEXMIFc.3554G>A (p.Gly1185Glu)
Xg.74741004C>ACA413665456NEXMIFc.3553G>T (p.Gly1185Trp)
COSMIC
Xg.74741004C>GCA413665457NEXMIFc.3553G>C (p.Gly1185Arg)
Xg.74741004C>TCA413665458NEXMIFc.3553G>A (p.Gly1185Arg)
Xg.74741005A>CCA413665459NEXMIFc.3552T>G (p.Ser1184Arg)
Xg.74741005A>GCA517466150NEXMIFc.3552T>C (p.Ser1184=)
Xg.74741005A>TCA413665460NEXMIFc.3552T>A (p.Ser1184Arg)
Xg.74741006C>ACA413665464NEXMIFc.3551G>T (p.Ser1184Ile)
Xg.74741006C=CA2437590200NEXMIFc.3551G= (p.Ser1184=)
Xg.74741006C>GCA413665466NEXMIFc.3551G>C (p.Ser1184Thr)
Xg.74741006C>TCA413665468NEXMIFc.3551G>A (p.Ser1184Asn)
dbSNP gnomAD v2 gnomAD v4
Xg.74741007T>ACA413665470NEXMIFc.3550A>T (p.Ser1184Cys)
Xg.74741007T>CCA413665471NEXMIFc.3550A>G (p.Ser1184Gly)
Xg.74741007T>GCA413665473NEXMIFc.3550A>C (p.Ser1184Arg)
Xg.74741008C>ACA413665476NEXMIFc.3549G>T (p.Lys1183Asn)
Xg.74741008C>GCA413665475NEXMIFc.3549G>C (p.Lys1183Asn)
Xg.74741008C>TCA517466154NEXMIFc.3549G>A (p.Lys1183=)
Xg.74741009T>ACA413665478NEXMIFc.3548A>T (p.Lys1183Met)
Xg.74741009T>CCA413665480NEXMIFc.3548A>G (p.Lys1183Arg)
Xg.74741009T>GCA413665482NEXMIFc.3548A>C (p.Lys1183Thr)
Xg.74741010T>ACA413665484NEXMIFc.3547A>T (p.Lys1183Ter)
Xg.74741010T>CCA413665487NEXMIFc.3547A>G (p.Lys1183Glu)
Xg.74741010T>GCA413665489NEXMIFc.3547A>C (p.Lys1183Gln)
Xg.74741011G>ACA517466155NEXMIFc.3546C>T (p.Ser1182=)
Xg.74741011G>CCA413665491NEXMIFc.3546C>G (p.Ser1182Arg)
dbSNP gnomAD v4
Xg.74741011G=CA2437590201NEXMIFc.3546C= (p.Ser1182=)
Xg.74741011G>TCA413665492NEXMIFc.3546C>A (p.Ser1182Arg)
Xg.74741012C>ACA10454933NEXMIFc.3545G>T (p.Ser1182Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74741012C=CA2437590202NEXMIFc.3545G= (p.Ser1182=)
Xg.74741012C>GCA413665494NEXMIFc.3545G>C (p.Ser1182Thr)
Xg.74741012C>TCA413665495NEXMIFc.3545G>A (p.Ser1182Asn)
gnomAD v4
Xg.74741013T>ACA413665496NEXMIFc.3544A>T (p.Ser1182Cys)
Xg.74741013T>CCA413665498NEXMIFc.3544A>G (p.Ser1182Gly)
Xg.74741013T>GCA413665499NEXMIFc.3544A>C (p.Ser1182Arg)
Xg.74741014G>ACA517466159NEXMIFc.3543C>T (p.Pro1181=)
Xg.74741014G>CCA517466160NEXMIFc.3543C>G (p.Pro1181=)
COSMIC
Xg.74741014G>TCA517466158NEXMIFc.3543C>A (p.Pro1181=)
gnomAD v4
Xg.74741015G>ACA413665502NEXMIFc.3542C>T (p.Pro1181Leu)
gnomAD v4
Xg.74741015G>CCA413665504NEXMIFc.3542C>G (p.Pro1181Arg)
dbSNP
Xg.74741015G=CA2437590203NEXMIFc.3542C= (p.Pro1181=)
Xg.74741015G>TCA413665501NEXMIFc.3542C>A (p.Pro1181His)
Xg.74741016G>ACA413665506NEXMIFc.3541C>T (p.Pro1181Ser)
Xg.74741016G>CCA413665509NEXMIFc.3541C>G (p.Pro1181Ala)
gnomAD v4
Xg.74741016G>TCA413665508NEXMIFc.3541C>A (p.Pro1181Thr)
Xg.74741017T>ACA517466165NEXMIFc.3540A>T (p.Ser1180=)
Xg.74741017T>CCA517466162NEXMIFc.3540A>G (p.Ser1180=)
Xg.74741017T>GCA517466163NEXMIFc.3540A>C (p.Ser1180=)
gnomAD v4
Xg.74741018G>ACA413665512NEXMIFc.3539C>T (p.Ser1180Leu)
COSMIC
Xg.74741018G>CCA413665514NEXMIFc.3539C>G (p.Ser1180Ter)
Xg.74741018G>TCA413665513NEXMIFc.3539C>A (p.Ser1180Ter)
ClinVar
Xg.74741019A>CCA413665516NEXMIFc.3538T>G (p.Ser1180Ala)
Xg.74741019A>GCA413665518NEXMIFc.3538T>C (p.Ser1180Pro)
Xg.74741019A>TCA413665520NEXMIFc.3538T>A (p.Ser1180Thr)
Xg.74741020A>CCA413665521NEXMIFc.3537T>G (p.Ser1179Arg)
Xg.74741020A>GCA517466166NEXMIFc.3537T>C (p.Ser1179=)
Xg.74741020A>TCA413665523NEXMIFc.3537T>A (p.Ser1179Arg)
Xg.74741021C>ACA413665524NEXMIFc.3536G>T (p.Ser1179Ile)
COSMIC
Xg.74741021C>GCA413665526NEXMIFc.3536G>C (p.Ser1179Thr)
gnomAD v4
Xg.74741021C>TCA413665528NEXMIFc.3536G>A (p.Ser1179Asn)
Xg.74741022T>ACA413665529NEXMIFc.3535A>T (p.Ser1179Cys)
Xg.74741022T>CCA413665530NEXMIFc.3535A>G (p.Ser1179Gly)
dbSNP gnomAD v2 gnomAD v4
Xg.74741022T>GCA413665531NEXMIFc.3535A>C (p.Ser1179Arg)
COSMIC
Xg.74741022T=CA2437590204NEXMIFc.3535A= (p.Ser1179=)
Xg.74741023T>ACA413665534NEXMIFc.3534A>T (p.Lys1178Asn)
Xg.74741023T>CCA517466172NEXMIFc.3534A>G (p.Lys1178=)
Xg.74741023T>GCA413665536NEXMIFc.3534A>C (p.Lys1178Asn)
Xg.74741024T>ACA413665539NEXMIFc.3533A>T (p.Lys1178Ile)
Xg.74741024T>CCA10454934NEXMIFc.3533A>G (p.Lys1178Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
Xg.74741024T>GCA413665541NEXMIFc.3533A>C (p.Lys1178Thr)
Xg.74741024T=CA2437590205NEXMIFc.3533A= (p.Lys1178=)
Xg.74741025T>ACA413665544NEXMIFc.3532A>T (p.Lys1178Ter)
Xg.74741025T>CCA413665546NEXMIFc.3532A>G (p.Lys1178Glu)
Xg.74741025T>GCA413665548NEXMIFc.3532A>C (p.Lys1178Gln)
Xg.74741026C>ACA413665549NEXMIFc.3531G>T (p.Lys1177Asn)
Xg.74741026C>GCA413665550NEXMIFc.3531G>C (p.Lys1177Asn)
Xg.74741026C>TCA517466173NEXMIFc.3531G>A (p.Lys1177=)
gnomAD v4
Xg.74741027T>ACA413665552NEXMIFc.3530A>T (p.Lys1177Met)
Xg.74741027T>CCA413665554NEXMIFc.3530A>G (p.Lys1177Arg)
gnomAD v4
Xg.74741027T>GCA413665556NEXMIFc.3530A>C (p.Lys1177Thr)
Xg.74741028T>ACA413665558NEXMIFc.3529A>T (p.Lys1177Ter)
Xg.74741028T>CCA413665559NEXMIFc.3529A>G (p.Lys1177Glu)
Xg.74741028T>GCA413665561NEXMIFc.3529A>C (p.Lys1177Gln)
Xg.74741029T>ACA413665562NEXMIFc.3528A>T (p.Arg1176Ser)
Xg.74741029T>CCA517466176NEXMIFc.3528A>G (p.Arg1176=)
Xg.74741029T>GCA413665564NEXMIFc.3528A>C (p.Arg1176Ser)
Xg.74741030C>ACA413665565NEXMIFc.3527G>T (p.Arg1176Ile)
Xg.74741030C>GCA413665566NEXMIFc.3527G>C (p.Arg1176Thr)
Xg.74741030C>TCA413665567NEXMIFc.3527G>A (p.Arg1176Lys)
Xg.74741031T>ACA413665568NEXMIFc.3526A>T (p.Arg1176Ter)
Xg.74741031T>CCA413665569NEXMIFc.3526A>G (p.Arg1176Gly)
Xg.74741031T>GCA517466183NEXMIFc.3526A>C (p.Arg1176=)
Xg.74741032T>ACA517466185NEXMIFc.3525A>T (p.Ser1175=)
Xg.74741032T>CCA517466186NEXMIFc.3525A>G (p.Ser1175=)
Xg.74741032T>GCA517466187NEXMIFc.3525A>C (p.Ser1175=)
Xg.74741033G>ACA413665570NEXMIFc.3524C>T (p.Ser1175Leu)
Xg.74741033G>CCA413665571NEXMIFc.3524C>G (p.Ser1175Ter)
Xg.74741033G=CA2437590206NEXMIFc.3524C= (p.Ser1175=)
Xg.74741033G>TCA413665573NEXMIFc.3524C>A (p.Ser1175Ter)
ClinVar dbSNP
Xg.74741034A>CCA413665575NEXMIFc.3523T>G (p.Ser1175Ala)
Xg.74741034A>GCA413665577NEXMIFc.3523T>C (p.Ser1175Pro)
Xg.74741034A>TCA413665579NEXMIFc.3523T>A (p.Ser1175Thr)
Xg.74741035T>ACA413665580NEXMIFc.3522A>T (p.Lys1174Asn)
Xg.74741035T>CCA517466188NEXMIFc.3522A>G (p.Lys1174=)
Xg.74741035T>GCA413665582NEXMIFc.3522A>C (p.Lys1174Asn)
Xg.74741036T>ACA413665588NEXMIFc.3521A>T (p.Lys1174Ile)
Xg.74741036T>CCA413665585NEXMIFc.3521A>G (p.Lys1174Arg)
Xg.74741036T>GCA413665586NEXMIFc.3521A>C (p.Lys1174Thr)
dbSNP gnomAD v2 gnomAD v4
Xg.74741036T=CA2437590207NEXMIFc.3521A= (p.Lys1174=)
Xg.74741037T>ACA413665590NEXMIFc.3520A>T (p.Lys1174Ter)
Xg.74741037T>CCA413665591NEXMIFc.3520A>G (p.Lys1174Glu)
Xg.74741037T>GCA413665593NEXMIFc.3520A>C (p.Lys1174Gln)
Xg.74741038T>ACA517466190NEXMIFc.3519A>T (p.Ser1173=)
Xg.74741038T>CCA517466191NEXMIFc.3519A>G (p.Ser1173=)
Xg.74741038T>GCA517466193NEXMIFc.3519A>C (p.Ser1173=)
Xg.74741039G>ACA413665595NEXMIFc.3518C>T (p.Ser1173Leu)
Xg.74741039G>CCA413665597NEXMIFc.3518C>G (p.Ser1173Ter)
Xg.74741039G>TCA413665599NEXMIFc.3518C>A (p.Ser1173Ter)
Xg.74741040A>CCA413665601NEXMIFc.3517T>G (p.Ser1173Ala)
Xg.74741040A>GCA413665602NEXMIFc.3517T>C (p.Ser1173Pro)
COSMIC
Xg.74741040A>TCA413665604NEXMIFc.3517T>A (p.Ser1173Thr)
Xg.74741041C>ACA517466196NEXMIFc.3516G>T (p.Val1172=)
Xg.74741041C>GCA517466194NEXMIFc.3516G>C (p.Val1172=)
Xg.74741041C>TCA517466195NEXMIFc.3516G>A (p.Val1172=)
gnomAD v4
Xg.74741042A>CCA413665606NEXMIFc.3515T>G (p.Val1172Gly)
Xg.74741042A>GCA413665608NEXMIFc.3515T>C (p.Val1172Ala)
Xg.74741042A>TCA413665609NEXMIFc.3515T>A (p.Val1172Glu)
Xg.74741043C>ACA413665611NEXMIFc.3514G>T (p.Val1172Leu)
Xg.74741043C>GCA413665615NEXMIFc.3514G>C (p.Val1172Leu)
ClinVar
Xg.74741043C>TCA413665613NEXMIFc.3514G>A (p.Val1172Met)
Xg.74741044T>ACA413665616NEXMIFc.3513A>T (p.Lys1171Asn)
Xg.74741044T>CCA517466201NEXMIFc.3513A>G (p.Lys1171=)
Xg.74741044T>GCA413665618NEXMIFc.3513A>C (p.Lys1171Asn)
Xg.74741044_74741046delCA2694119726NEXMIFc.3511_3513del (p.Lys1171del)
gnomAD v4
Xg.74741045T>ACA413665620NEXMIFc.3512A>T (p.Lys1171Ile)
Xg.74741045T>CCA413665622NEXMIFc.3512A>G (p.Lys1171Arg)
Xg.74741045T>GCA413665623NEXMIFc.3512A>C (p.Lys1171Thr)
Xg.74741046T>ACA413665626NEXMIFc.3511A>T (p.Lys1171Ter)
Xg.74741046T>CCA413665628NEXMIFc.3511A>G (p.Lys1171Glu)
Xg.74741046T>GCA413665629NEXMIFc.3511A>C (p.Lys1171Gln)
Xg.74741047G>ACA517466204NEXMIFc.3510C>T (p.Asn1170=)
Xg.74741047G>CCA413665630NEXMIFc.3510C>G (p.Asn1170Lys)
Xg.74741047G=CA2437590208NEXMIFc.3510C= (p.Asn1170=)
Xg.74741047G>TCA413665632NEXMIFc.3510C>A (p.Asn1170Lys)
dbSNP gnomAD v2 gnomAD v4 COSMIC
Xg.74741048T>ACA413665633NEXMIFc.3509A>T (p.Asn1170Ile)
Xg.74741048T>CCA413665635NEXMIFc.3509A>G (p.Asn1170Ser)
gnomAD v4
Xg.74741048T>GCA413665636NEXMIFc.3509A>C (p.Asn1170Thr)
Xg.74741049T>ACA413665641NEXMIFc.3508A>T (p.Asn1170Tyr)
Xg.74741049T>CCA413665637NEXMIFc.3508A>G (p.Asn1170Asp)
Xg.74741049T>GCA413665639NEXMIFc.3508A>C (p.Asn1170His)
Xg.74741050G>ACA10454935NEXMIFc.3507C>T (p.Asn1169=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.74741050G>CCA413665643NEXMIFc.3507C>G (p.Asn1169Lys)
Xg.74741050G=CA2437590209NEXMIFc.3507C= (p.Asn1169=)
Xg.74741050G>TCA413665645NEXMIFc.3507C>A (p.Asn1169Lys)
ClinVar
Xg.74741051T>ACA413665648NEXMIFc.3506A>T (p.Asn1169Ile)
Xg.74741051T>CCA413665649NEXMIFc.3506A>G (p.Asn1169Ser)
Xg.74741051T>GCA413665650NEXMIFc.3506A>C (p.Asn1169Thr)
Xg.74741052T>ACA413665653NEXMIFc.3505A>T (p.Asn1169Tyr)
Xg.74741052T>CCA413665654NEXMIFc.3505A>G (p.Asn1169Asp)
Xg.74741052T>GCA413665655NEXMIFc.3505A>C (p.Asn1169His)
Xg.74741053G>ACA517466212NEXMIFc.3504C>T (p.Thr1168=)
gnomAD v4
Xg.74741053G>CCA517466213NEXMIFc.3504C>G (p.Thr1168=)
Xg.74741053G>TCA517466214NEXMIFc.3504C>A (p.Thr1168=)
Xg.74741054G>ACA413665658NEXMIFc.3503C>T (p.Thr1168Ile)
Xg.74741054G>CCA413665660NEXMIFc.3503C>G (p.Thr1168Ser)
Xg.74741054G=CA2437590210NEXMIFc.3503C= (p.Thr1168=)
Xg.74741054G>TCA10454936NEXMIFc.3503C>A (p.Thr1168Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.74741055T>ACA413665662NEXMIFc.3502A>T (p.Thr1168Ser)
Xg.74741055T>CCA413665665NEXMIFc.3502A>G (p.Thr1168Ala)
dbSNP
Xg.74741055T>GCA413665664NEXMIFc.3502A>C (p.Thr1168Pro)
Xg.74741055T=CA2437590211NEXMIFc.3502A= (p.Thr1168=)
Xg.74741056A=CA2437590212NEXMIFc.3501T= (p.Ser1167=)
Xg.74741056A>CCA413665667NEXMIFc.3501T>G (p.Ser1167Arg)
Xg.74741056A>GCA517466219NEXMIFc.3501T>C (p.Ser1167=)
Xg.74741056A>TCA10454937NEXMIFc.3501T>A (p.Ser1167Arg)
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched