Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.44953066G>ACA402325053SETBP1c.3726G>A (p.Trp1242Ter)
c.3804G>A (p.Trp1268Ter)
c.3249G>A (p.Trp1083Ter)
 dbSNP gnomAD v2
18g.44953066G>CCA402325052SETBP1c.3726G>C (p.Trp1242Cys)
c.3804G>C (p.Trp1268Cys)
c.3249G>C (p.Trp1083Cys)
 dbSNP gnomAD v4
18g.44953066G=CA2300141242SETBP1c.3726G= (p.Trp1242=)
c.3804G= (p.Trp1268=)
c.3249G= (p.Trp1083=)
18g.44953066G>TCA402325051SETBP1c.3726G>T (p.Trp1242Cys)
c.3804G>T (p.Trp1268Cys)
c.3249G>T (p.Trp1083Cys)
 dbSNP gnomAD v2 gnomAD v4
18g.44953067A>CCA402325054SETBP1c.3727A>C (p.Thr1243Pro)
c.3805A>C (p.Thr1269Pro)
c.3250A>C (p.Thr1084Pro)
18g.44953067A>GCA402325055SETBP1c.3727A>G (p.Thr1243Ala)
c.3805A>G (p.Thr1269Ala)
c.3250A>G (p.Thr1084Ala)
18g.44953067A>TCA402325056SETBP1c.3727A>T (p.Thr1243Ser)
c.3805A>T (p.Thr1269Ser)
c.3250A>T (p.Thr1084Ser)
18g.44953068C>ACA402325057SETBP1c.3728C>A (p.Thr1243Lys)
c.3806C>A (p.Thr1269Lys)
c.3251C>A (p.Thr1084Lys)
18g.44953068C=CA2300141243SETBP1c.3728C= (p.Thr1243=)
c.3806C= (p.Thr1269=)
c.3251C= (p.Thr1084=)
18g.44953068C>GCA402325058SETBP1c.3728C>G (p.Thr1243Arg)
c.3806C>G (p.Thr1269Arg)
c.3251C>G (p.Thr1084Arg)
18g.44953068C>TCA8945970SETBP1c.3728C>T (p.Thr1243Ile)
c.3806C>T (p.Thr1269Ile)
c.3251C>T (p.Thr1084Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953069A>CCA503982907SETBP1c.3729A>C (p.Thr1243=)
c.3807A>C (p.Thr1269=)
c.3252A>C (p.Thr1084=)
18g.44953069A>GCA503982908SETBP1c.3729A>G (p.Thr1243=)
c.3807A>G (p.Thr1269=)
c.3252A>G (p.Thr1084=)
 gnomAD v4
18g.44953069A>TCA503982909SETBP1c.3729A>T (p.Thr1243=)
c.3807A>T (p.Thr1269=)
c.3252A>T (p.Thr1084=)
18g.44953070C>ACA402325059SETBP1c.3730C>A (p.Gln1244Lys)
c.3808C>A (p.Gln1270Lys)
c.3253C>A (p.Gln1085Lys)
18g.44953070C>GCA402325060SETBP1c.3730C>G (p.Gln1244Glu)
c.3808C>G (p.Gln1270Glu)
c.3253C>G (p.Gln1085Glu)
 ClinVar dbSNP
18g.44953070C>TCA402325061SETBP1c.3730C>T (p.Gln1244Ter)
c.3808C>T (p.Gln1270Ter)
c.3253C>T (p.Gln1085Ter)
18g.44953071A=CA2300141244SETBP1c.3731A= (p.Gln1244=)
c.3809A= (p.Gln1270=)
c.3254A= (p.Gln1085=)
18g.44953071A>CCA402325062SETBP1c.3731A>C (p.Gln1244Pro)
c.3809A>C (p.Gln1270Pro)
c.3254A>C (p.Gln1085Pro)
18g.44953071A>GCA8945971SETBP1c.3731A>G (p.Gln1244Arg)
c.3809A>G (p.Gln1270Arg)
c.3254A>G (p.Gln1085Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.44953071A>TCA402325063SETBP1c.3731A>T (p.Gln1244Leu)
c.3809A>T (p.Gln1270Leu)
c.3254A>T (p.Gln1085Leu)
18g.44953071dupCA2573054662SETBP1c.3731dup (p.Ala1245GlyfsTer10)
c.3809dup (p.Ala1271GlyfsTer10)
c.3254dup (p.Ala1086GlyfsTer10)
 ClinVar dbSNP
18g.44953072G>ACA503982911SETBP1c.3732G>A (p.Gln1244=)
c.3810G>A (p.Gln1270=)
c.3255G>A (p.Gln1085=)
18g.44953072G>CCA402325064SETBP1c.3732G>C (p.Gln1244His)
c.3810G>C (p.Gln1270His)
c.3255G>C (p.Gln1085His)
18g.44953072G>TCA402325065SETBP1c.3732G>T (p.Gln1244His)
c.3810G>T (p.Gln1270His)
c.3255G>T (p.Gln1085His)
18g.44953073G>ACA402325066SETBP1c.3733G>A (p.Ala1245Thr)
c.3811G>A (p.Ala1271Thr)
c.3256G>A (p.Ala1086Thr)
 dbSNP gnomAD v4
18g.44953073G>CCA402325067SETBP1c.3733G>C (p.Ala1245Pro)
c.3811G>C (p.Ala1271Pro)
c.3256G>C (p.Ala1086Pro)
18g.44953073G=CA2300141245SETBP1c.3733G= (p.Ala1245=)
c.3811G= (p.Ala1271=)
c.3256G= (p.Ala1086=)
18g.44953073G>TCA402325068SETBP1c.3733G>T (p.Ala1245Ser)
c.3811G>T (p.Ala1271Ser)
c.3256G>T (p.Ala1086Ser)
18g.44953074C>ACA402325069SETBP1c.3734C>A (p.Ala1245Asp)
c.3812C>A (p.Ala1271Asp)
c.3257C>A (p.Ala1086Asp)
18g.44953074C=CA2300141246SETBP1c.3734C= (p.Ala1245=)
c.3812C= (p.Ala1271=)
c.3257C= (p.Ala1086=)
18g.44953074C>GCA402325070SETBP1c.3734C>G (p.Ala1245Gly)
c.3812C>G (p.Ala1271Gly)
c.3257C>G (p.Ala1086Gly)
18g.44953074C>TCA402325071SETBP1c.3734C>T (p.Ala1245Val)
c.3812C>T (p.Ala1271Val)
c.3257C>T (p.Ala1086Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953075C>ACA503982913SETBP1c.3735C>A (p.Ala1245=)
c.3813C>A (p.Ala1271=)
c.3258C>A (p.Ala1086=)
18g.44953075C>GCA503982914SETBP1c.3735C>G (p.Ala1245=)
c.3813C>G (p.Ala1271=)
c.3258C>G (p.Ala1086=)
18g.44953075C>TCA503982915SETBP1c.3735C>T (p.Ala1245=)
c.3813C>T (p.Ala1271=)
c.3258C>T (p.Ala1086=)
18g.44953076A=CA2300141247SETBP1c.3736A= (p.Lys1246=)
c.3814A= (p.Lys1272=)
c.3259A= (p.Lys1087=)
18g.44953076A>CCA402325073SETBP1c.3736A>C (p.Lys1246Gln)
c.3814A>C (p.Lys1272Gln)
c.3259A>C (p.Lys1087Gln)
18g.44953076A>GCA8945972SETBP1c.3736A>G (p.Lys1246Glu)
c.3814A>G (p.Lys1272Glu)
c.3259A>G (p.Lys1087Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953076A>TCA402325072SETBP1c.3736A>T (p.Lys1246Ter)
c.3814A>T (p.Lys1272Ter)
c.3259A>T (p.Lys1087Ter)
18g.44953077delCA2812320165SETBP1c.3737del (p.Lys1246ArgfsTer6)
c.3815del (p.Lys1272ArgfsTer6)
c.3260del (p.Lys1087ArgfsTer6)
18g.44953077A=CA2300141248SETBP1c.3737A= (p.Lys1246=)
c.3815A= (p.Lys1272=)
c.3260A= (p.Lys1087=)
18g.44953077A>CCA402325074SETBP1c.3737A>C (p.Lys1246Thr)
c.3815A>C (p.Lys1272Thr)
c.3260A>C (p.Lys1087Thr)
18g.44953077A>GCA299699730SETBP1c.3737A>G (p.Lys1246Arg)
c.3815A>G (p.Lys1272Arg)
c.3260A>G (p.Lys1087Arg)
 dbSNP gnomAD v2 gnomAD v4
18g.44953077A>TCA402325075SETBP1c.3737A>T (p.Lys1246Met)
c.3815A>T (p.Lys1272Met)
c.3260A>T (p.Lys1087Met)
18g.44953078G>ACA503982917SETBP1c.3738G>A (p.Lys1246=)
c.3816G>A (p.Lys1272=)
c.3261G>A (p.Lys1087=)
18g.44953078G>CCA402325076SETBP1c.3738G>C (p.Lys1246Asn)
c.3816G>C (p.Lys1272Asn)
c.3261G>C (p.Lys1087Asn)
18g.44953078G>TCA402325077SETBP1c.3738G>T (p.Lys1246Asn)
c.3816G>T (p.Lys1272Asn)
c.3261G>T (p.Lys1087Asn)
18g.44953079G>ACA402325078SETBP1c.3739G>A (p.Glu1247Lys)
c.3817G>A (p.Glu1273Lys)
c.3262G>A (p.Glu1088Lys)
 COSMIC
18g.44953079G>CCA402325080SETBP1c.3739G>C (p.Glu1247Gln)
c.3817G>C (p.Glu1273Gln)
c.3262G>C (p.Glu1088Gln)
18g.44953079G>TCA402325079SETBP1c.3739G>T (p.Glu1247Ter)
c.3817G>T (p.Glu1273Ter)
c.3262G>T (p.Glu1088Ter)
18g.44953080A>CCA402325081SETBP1c.3740A>C (p.Glu1247Ala)
c.3818A>C (p.Glu1273Ala)
c.3263A>C (p.Glu1088Ala)
18g.44953080A>GCA402325082SETBP1c.3740A>G (p.Glu1247Gly)
c.3818A>G (p.Glu1273Gly)
c.3263A>G (p.Glu1088Gly)
 ClinVar dbSNP gnomAD v4
18g.44953080A>TCA402325083SETBP1c.3740A>T (p.Glu1247Val)
c.3818A>T (p.Glu1273Val)
c.3263A>T (p.Glu1088Val)
18g.44953084delCA503982921SETBP1c.3744del (p.Gly1249GlufsTer3)
c.3822del (p.Gly1275GlufsTer3)
c.3267del (p.Gly1090GlufsTer3)
 COSMIC
18g.44953081A>CCA402325084SETBP1c.3741A>C (p.Glu1247Asp)
c.3819A>C (p.Glu1273Asp)
c.3264A>C (p.Glu1088Asp)
18g.44953081A>GCA503982924SETBP1c.3741A>G (p.Glu1247=)
c.3819A>G (p.Glu1273=)
c.3264A>G (p.Glu1088=)
 gnomAD v4
18g.44953081A>TCA402325085SETBP1c.3741A>T (p.Glu1247Asp)
c.3819A>T (p.Glu1273Asp)
c.3264A>T (p.Glu1088Asp)
18g.44953082A>CCA402325086SETBP1c.3742A>C (p.Lys1248Gln)
c.3820A>C (p.Lys1274Gln)
c.3265A>C (p.Lys1089Gln)
18g.44953082A>GCA402325087SETBP1c.3742A>G (p.Lys1248Glu)
c.3820A>G (p.Lys1274Glu)
c.3265A>G (p.Lys1089Glu)
18g.44953082A>TCA402325088SETBP1c.3742A>T (p.Lys1248Ter)
c.3820A>T (p.Lys1274Ter)
c.3265A>T (p.Lys1089Ter)
18g.44953083A>CCA402325089SETBP1c.3743A>C (p.Lys1248Thr)
c.3821A>C (p.Lys1274Thr)
c.3266A>C (p.Lys1089Thr)
18g.44953083A>GCA402325090SETBP1c.3743A>G (p.Lys1248Arg)
c.3821A>G (p.Lys1274Arg)
c.3266A>G (p.Lys1089Arg)
18g.44953083A>TCA402325091SETBP1c.3743A>T (p.Lys1248Ile)
c.3821A>T (p.Lys1274Ile)
c.3266A>T (p.Lys1089Ile)
18g.44953084A=CA2300141249SETBP1c.3744A= (p.Lys1248=)
c.3822A= (p.Lys1274=)
c.3267A= (p.Lys1089=)
18g.44953084A>CCA402325093SETBP1c.3744A>C (p.Lys1248Asn)
c.3822A>C (p.Lys1274Asn)
c.3267A>C (p.Lys1089Asn)
18g.44953084A>GCA8945973SETBP1c.3744A>G (p.Lys1248=)
c.3822A>G (p.Lys1274=)
c.3267A>G (p.Lys1089=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953084A>TCA402325092SETBP1c.3744A>T (p.Lys1248Asn)
c.3822A>T (p.Lys1274Asn)
c.3267A>T (p.Lys1089Asn)
18g.44953085G>ACA402325094SETBP1c.3745G>A (p.Gly1249Arg)
c.3823G>A (p.Gly1275Arg)
c.3268G>A (p.Gly1090Arg)
18g.44953085G>CCA402325095SETBP1c.3745G>C (p.Gly1249Arg)
c.3823G>C (p.Gly1275Arg)
c.3268G>C (p.Gly1090Arg)
18g.44953085G>TCA402325096SETBP1c.3745G>T (p.Gly1249Ter)
c.3823G>T (p.Gly1275Ter)
c.3268G>T (p.Gly1090Ter)
18g.44953086G>ACA402325097SETBP1c.3746G>A (p.Gly1249Glu)
c.3824G>A (p.Gly1275Glu)
c.3269G>A (p.Gly1090Glu)
18g.44953086G>CCA402325098SETBP1c.3746G>C (p.Gly1249Ala)
c.3824G>C (p.Gly1275Ala)
c.3269G>C (p.Gly1090Ala)
18g.44953086G>TCA402325099SETBP1c.3746G>T (p.Gly1249Val)
c.3824G>T (p.Gly1275Val)
c.3269G>T (p.Gly1090Val)
18g.44953087A>CCA503982928SETBP1c.3747A>C (p.Gly1249=)
c.3825A>C (p.Gly1275=)
c.3270A>C (p.Gly1090=)
18g.44953087A>GCA503982929SETBP1c.3747A>G (p.Gly1249=)
c.3825A>G (p.Gly1275=)
c.3270A>G (p.Gly1090=)
18g.44953087A>TCA503982930SETBP1c.3747A>T (p.Gly1249=)
c.3825A>T (p.Gly1275=)
c.3270A>T (p.Gly1090=)
18g.44953088G>ACA402325100SETBP1c.3748G>A (p.Asp1250Asn)
c.3826G>A (p.Asp1276Asn)
c.3271G>A (p.Asp1091Asn)
 gnomAD v4
18g.44953088G>CCA402325101SETBP1c.3748G>C (p.Asp1250His)
c.3826G>C (p.Asp1276His)
c.3271G>C (p.Asp1091His)
 gnomAD v4 COSMIC
18g.44953088G>TCA402325102SETBP1c.3748G>T (p.Asp1250Tyr)
c.3826G>T (p.Asp1276Tyr)
c.3271G>T (p.Asp1091Tyr)
18g.44953089A>CCA402325103SETBP1c.3749A>C (p.Asp1250Ala)
c.3827A>C (p.Asp1276Ala)
c.3272A>C (p.Asp1091Ala)
18g.44953089A>GCA402325104SETBP1c.3749A>G (p.Asp1250Gly)
c.3827A>G (p.Asp1276Gly)
c.3272A>G (p.Asp1091Gly)
18g.44953089A>TCA402325105SETBP1c.3749A>T (p.Asp1250Val)
c.3827A>T (p.Asp1276Val)
c.3272A>T (p.Asp1091Val)
18g.44953090C>ACA402325106SETBP1c.3750C>A (p.Asp1250Glu)
c.3828C>A (p.Asp1276Glu)
c.3273C>A (p.Asp1091Glu)
18g.44953090C=CA2300141250SETBP1c.3750C= (p.Asp1250=)
c.3828C= (p.Asp1276=)
c.3273C= (p.Asp1091=)
18g.44953090C>GCA402325107SETBP1c.3750C>G (p.Asp1250Glu)
c.3828C>G (p.Asp1276Glu)
c.3273C>G (p.Asp1091Glu)
18g.44953090C>TCA8945974SETBP1c.3750C>T (p.Asp1250=)
c.3828C>T (p.Asp1276=)
c.3273C>T (p.Asp1091=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953091T>ACA402325108SETBP1c.3751T>A (p.Leu1251Met)
c.3829T>A (p.Leu1277Met)
c.3274T>A (p.Leu1092Met)
18g.44953091T>CCA503982934SETBP1c.3751T>C (p.Leu1251=)
c.3829T>C (p.Leu1277=)
c.3274T>C (p.Leu1092=)
18g.44953091T>GCA402325109SETBP1c.3751T>G (p.Leu1251Val)
c.3829T>G (p.Leu1277Val)
c.3274T>G (p.Leu1092Val)
 dbSNP
18g.44953091T=CA2300141251SETBP1c.3751T= (p.Leu1251=)
c.3829T= (p.Leu1277=)
c.3274T= (p.Leu1092=)
18g.44953092T>ACA402325110SETBP1c.3752T>A (p.Leu1251Ter)
c.3830T>A (p.Leu1277Ter)
c.3275T>A (p.Leu1092Ter)
18g.44953092T>CCA402325111SETBP1c.3752T>C (p.Leu1251Ser)
c.3830T>C (p.Leu1277Ser)
c.3275T>C (p.Leu1092Ser)
18g.44953092T>GCA402325112SETBP1c.3752T>G (p.Leu1251Trp)
c.3830T>G (p.Leu1277Trp)
c.3275T>G (p.Leu1092Trp)
18g.44953093G>ACA503982935SETBP1c.3753G>A (p.Leu1251=)
c.3831G>A (p.Leu1277=)
c.3276G>A (p.Leu1092=)
18g.44953093G>CCA402325113SETBP1c.3753G>C (p.Leu1251Phe)
c.3831G>C (p.Leu1277Phe)
c.3276G>C (p.Leu1092Phe)
18g.44953093G>TCA402325114SETBP1c.3753G>T (p.Leu1251Phe)
c.3831G>T (p.Leu1277Phe)
c.3276G>T (p.Leu1092Phe)
18g.44953094A>CCA402325115SETBP1c.3754A>C (p.Ser1252Arg)
c.3832A>C (p.Ser1278Arg)
c.3277A>C (p.Ser1093Arg)
18g.44953094A>GCA402325116SETBP1c.3754A>G (p.Ser1252Gly)
c.3832A>G (p.Ser1278Gly)
c.3277A>G (p.Ser1093Gly)
18g.44953094A>TCA402325117SETBP1c.3754A>T (p.Ser1252Cys)
c.3832A>T (p.Ser1278Cys)
c.3277A>T (p.Ser1093Cys)
18g.44953095G>ACA8945975SETBP1c.3755G>A (p.Ser1252Asn)
c.3833G>A (p.Ser1278Asn)
c.3278G>A (p.Ser1093Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953095G>CCA402325118SETBP1c.3755G>C (p.Ser1252Thr)
c.3833G>C (p.Ser1278Thr)
c.3278G>C (p.Ser1093Thr)
18g.44953095G=CA2300141252SETBP1c.3755G= (p.Ser1252=)
c.3833G= (p.Ser1278=)
c.3278G= (p.Ser1093=)
18g.44953095G>TCA402325119SETBP1c.3755G>T (p.Ser1252Ile)
c.3833G>T (p.Ser1278Ile)
c.3278G>T (p.Ser1093Ile)
 gnomAD v4
18g.44953096C>ACA402325120SETBP1c.3756C>A (p.Ser1252Arg)
c.3834C>A (p.Ser1278Arg)
c.3279C>A (p.Ser1093Arg)
18g.44953096C>GCA402325121SETBP1c.3756C>G (p.Ser1252Arg)
c.3834C>G (p.Ser1278Arg)
c.3279C>G (p.Ser1093Arg)
18g.44953096C>TCA503982937SETBP1c.3756C>T (p.Ser1252=)
c.3834C>T (p.Ser1278=)
c.3279C>T (p.Ser1093=)
18g.44953097A>CCA402325122SETBP1c.3757A>C (p.Ser1253Arg)
c.3835A>C (p.Ser1279Arg)
c.3280A>C (p.Ser1094Arg)
18g.44953097A>GCA402325124SETBP1c.3757A>G (p.Ser1253Gly)
c.3835A>G (p.Ser1279Gly)
c.3280A>G (p.Ser1094Gly)
18g.44953097A>TCA402325123SETBP1c.3757A>T (p.Ser1253Cys)
c.3835A>T (p.Ser1279Cys)
c.3280A>T (p.Ser1094Cys)
18g.44953098G>ACA402325125SETBP1c.3758G>A (p.Ser1253Asn)
c.3836G>A (p.Ser1279Asn)
c.3281G>A (p.Ser1094Asn)
 dbSNP gnomAD v2 gnomAD v4
18g.44953098G>CCA402325126SETBP1c.3758G>C (p.Ser1253Thr)
c.3836G>C (p.Ser1279Thr)
c.3281G>C (p.Ser1094Thr)
18g.44953098G=CA2300141253SETBP1c.3758G= (p.Ser1253=)
c.3836G= (p.Ser1279=)
c.3281G= (p.Ser1094=)
18g.44953098G>TCA402325127SETBP1c.3758G>T (p.Ser1253Ile)
c.3836G>T (p.Ser1279Ile)
c.3281G>T (p.Ser1094Ile)
18g.44953099T>ACA402325128SETBP1c.3759T>A (p.Ser1253Arg)
c.3837T>A (p.Ser1279Arg)
c.3282T>A (p.Ser1094Arg)
18g.44953099T>CCA503982941SETBP1c.3759T>C (p.Ser1253=)
c.3837T>C (p.Ser1279=)
c.3282T>C (p.Ser1094=)
18g.44953099T>GCA402325129SETBP1c.3759T>G (p.Ser1253Arg)
c.3837T>G (p.Ser1279Arg)
c.3282T>G (p.Ser1094Arg)
18g.44953100G>ACA402325130SETBP1c.3760G>A (p.Glu1254Lys)
c.3838G>A (p.Glu1280Lys)
c.3283G>A (p.Glu1095Lys)
 dbSNP gnomAD v2 gnomAD v4
18g.44953100G>CCA402325131SETBP1c.3760G>C (p.Glu1254Gln)
c.3838G>C (p.Glu1280Gln)
c.3283G>C (p.Glu1095Gln)
 dbSNP
18g.44953100G=CA2300141254SETBP1c.3760G= (p.Glu1254=)
c.3838G= (p.Glu1280=)
c.3283G= (p.Glu1095=)
18g.44953100G>TCA402325132SETBP1c.3760G>T (p.Glu1254Ter)
c.3838G>T (p.Glu1280Ter)
c.3283G>T (p.Glu1095Ter)
18g.44953101A>CCA402325133SETBP1c.3761A>C (p.Glu1254Ala)
c.3839A>C (p.Glu1280Ala)
c.3284A>C (p.Glu1095Ala)
18g.44953101A>GCA402325134SETBP1c.3761A>G (p.Glu1254Gly)
c.3839A>G (p.Glu1280Gly)
c.3284A>G (p.Glu1095Gly)
18g.44953101A>TCA402325135SETBP1c.3761A>T (p.Glu1254Val)
c.3839A>T (p.Glu1280Val)
c.3284A>T (p.Glu1095Val)
18g.44953102G>ACA503982943SETBP1c.3762G>A (p.Glu1254=)
c.3840G>A (p.Glu1280=)
c.3285G>A (p.Glu1095=)
 dbSNP gnomAD v3 gnomAD v4
18g.44953102G>CCA402325136SETBP1c.3762G>C (p.Glu1254Asp)
c.3840G>C (p.Glu1280Asp)
c.3285G>C (p.Glu1095Asp)
18g.44953102G=CA2300141255SETBP1c.3762G= (p.Glu1254=)
c.3840G= (p.Glu1280=)
c.3285G= (p.Glu1095=)
18g.44953102G>TCA402325137SETBP1c.3762G>T (p.Glu1254Asp)
c.3840G>T (p.Glu1280Asp)
c.3285G>T (p.Glu1095Asp)
 dbSNP
18g.44953103C>ACA402325140SETBP1c.3763C>A (p.Pro1255Thr)
c.3841C>A (p.Pro1281Thr)
c.3286C>A (p.Pro1096Thr)
18g.44953103C=CA2300141256SETBP1c.3763C= (p.Pro1255=)
c.3841C= (p.Pro1281=)
c.3286C= (p.Pro1096=)
18g.44953103C>GCA402325138SETBP1c.3763C>G (p.Pro1255Ala)
c.3841C>G (p.Pro1281Ala)
c.3286C>G (p.Pro1096Ala)
18g.44953103C>TCA402325139SETBP1c.3763C>T (p.Pro1255Ser)
c.3841C>T (p.Pro1281Ser)
c.3286C>T (p.Pro1096Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953104C>ACA402325141SETBP1c.3764C>A (p.Pro1255His)
c.3842C>A (p.Pro1281His)
c.3287C>A (p.Pro1096His)
 COSMIC
18g.44953104C>GCA402325142SETBP1c.3764C>G (p.Pro1255Arg)
c.3842C>G (p.Pro1281Arg)
c.3287C>G (p.Pro1096Arg)
18g.44953104C>TCA402325143SETBP1c.3764C>T (p.Pro1255Leu)
c.3842C>T (p.Pro1281Leu)
c.3287C>T (p.Pro1096Leu)
 COSMIC
18g.44953105T>ACA503982945SETBP1c.3765T>A (p.Pro1255=)
c.3843T>A (p.Pro1281=)
c.3288T>A (p.Pro1096=)
18g.44953105T>CCA503982946SETBP1c.3765T>C (p.Pro1255=)
c.3843T>C (p.Pro1281=)
c.3288T>C (p.Pro1096=)
 gnomAD v4
18g.44953105T>GCA503982948SETBP1c.3765T>G (p.Pro1255=)
c.3843T>G (p.Pro1281=)
c.3288T>G (p.Pro1096=)
18g.44953105T=CA2300141257SETBP1c.3765T= (p.Pro1255=)
c.3843T= (p.Pro1281=)
c.3288T= (p.Pro1096=)
18g.44953105dupCA2695227491SETBP1c.3765dup (p.Val1256CysfsTer28)
c.3843dup (p.Val1282CysfsTer28)
c.3288dup (p.Val1097CysfsTer28)
18g.44953106G>ACA402325144SETBP1c.3766G>A (p.Val1256Met)
c.3844G>A (p.Val1282Met)
c.3289G>A (p.Val1097Met)
 dbSNP
18g.44953106G>CCA402325145SETBP1c.3766G>C (p.Val1256Leu)
c.3844G>C (p.Val1282Leu)
c.3289G>C (p.Val1097Leu)
18g.44953106G=CA2300141258SETBP1c.3766G= (p.Val1256=)
c.3844G= (p.Val1282=)
c.3289G= (p.Val1097=)
18g.44953106G>TCA402325146SETBP1c.3766G>T (p.Val1256Leu)
c.3844G>T (p.Val1282Leu)
c.3289G>T (p.Val1097Leu)
18g.44953110_44953140dupCA1139666049SETBP1c.3770_3800dup (p.Gly1268LeufsTer26)
c.3848_3878dup (p.Gly1294LeufsTer26)
c.3293_3323dup (p.Gly1109LeufsTer26)
 ClinVar dbSNP
18g.44953107T>ACA402325147SETBP1c.3767T>A (p.Val1256Glu)
c.3845T>A (p.Val1282Glu)
c.3290T>A (p.Val1097Glu)
18g.44953107T>CCA8945976SETBP1c.3767T>C (p.Val1256Ala)
c.3845T>C (p.Val1282Ala)
c.3290T>C (p.Val1097Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953107T>GCA402325148SETBP1c.3767T>G (p.Val1256Gly)
c.3845T>G (p.Val1282Gly)
c.3290T>G (p.Val1097Gly)
18g.44953107T=CA2300141259SETBP1c.3767T= (p.Val1256=)
c.3845T= (p.Val1282=)
c.3290T= (p.Val1097=)
18g.44953108G>ACA503982949SETBP1c.3768G>A (p.Val1256=)
c.3846G>A (p.Val1282=)
c.3291G>A (p.Val1097=)
18g.44953108G>CCA503982950SETBP1c.3768G>C (p.Val1256=)
c.3846G>C (p.Val1282=)
c.3291G>C (p.Val1097=)
18g.44953108G>TCA503982951SETBP1c.3768G>T (p.Val1256=)
c.3846G>T (p.Val1282=)
c.3291G>T (p.Val1097=)
18g.44953109G>ACA402325149SETBP1c.3769G>A (p.Asp1257Asn)
c.3847G>A (p.Asp1283Asn)
c.3292G>A (p.Asp1098Asn)
18g.44953109G>CCA299699733SETBP1c.3769G>C (p.Asp1257His)
c.3847G>C (p.Asp1283His)
c.3292G>C (p.Asp1098His)
 dbSNP
18g.44953109G=CA2300141260SETBP1c.3769G= (p.Asp1257=)
c.3847G= (p.Asp1283=)
c.3292G= (p.Asp1098=)
18g.44953109G>TCA402325150SETBP1c.3769G>T (p.Asp1257Tyr)
c.3847G>T (p.Asp1283Tyr)
c.3292G>T (p.Asp1098Tyr)
 gnomAD v4
18g.44953110A=CA2300141261SETBP1c.3770A= (p.Asp1257=)
c.3848A= (p.Asp1283=)
c.3293A= (p.Asp1098=)
18g.44953110A>CCA402325152SETBP1c.3770A>C (p.Asp1257Ala)
c.3848A>C (p.Asp1283Ala)
c.3293A>C (p.Asp1098Ala)
18g.44953110A>GCA8945977SETBP1c.3770A>G (p.Asp1257Gly)
c.3848A>G (p.Asp1283Gly)
c.3293A>G (p.Asp1098Gly)
 ClinVar dbSNP ExAC gnomAD v2
18g.44953110A>TCA402325151SETBP1c.3770A>T (p.Asp1257Val)
c.3848A>T (p.Asp1283Val)
c.3293A>T (p.Asp1098Val)
18g.44953111C>ACA402325153SETBP1c.3771C>A (p.Asp1257Glu)
c.3849C>A (p.Asp1283Glu)
c.3294C>A (p.Asp1098Glu)
18g.44953111C>GCA402325154SETBP1c.3771C>G (p.Asp1257Glu)
c.3849C>G (p.Asp1283Glu)
c.3294C>G (p.Asp1098Glu)
18g.44953111C>TCA503982953SETBP1c.3771C>T (p.Asp1257=)
c.3849C>T (p.Asp1283=)
c.3294C>T (p.Asp1098=)
18g.44953112T>ACA402325155SETBP1c.3772T>A (p.Ser1258Thr)
c.3850T>A (p.Ser1284Thr)
c.3295T>A (p.Ser1099Thr)
18g.44953112T>CCA402325156SETBP1c.3772T>C (p.Ser1258Pro)
c.3850T>C (p.Ser1284Pro)
c.3295T>C (p.Ser1099Pro)
18g.44953112T>GCA402325157SETBP1c.3772T>G (p.Ser1258Ala)
c.3850T>G (p.Ser1284Ala)
c.3295T>G (p.Ser1099Ala)
18g.44953113C>ACA402325158SETBP1c.3773C>A (p.Ser1258Ter)
c.3851C>A (p.Ser1284Ter)
c.3296C>A (p.Ser1099Ter)
18g.44953113C=CA2300141262SETBP1c.3773C= (p.Ser1258=)
c.3851C= (p.Ser1284=)
c.3296C= (p.Ser1099=)
18g.44953113C>GCA402325159SETBP1c.3773C>G (p.Ser1258Ter)
c.3851C>G (p.Ser1284Ter)
c.3296C>G (p.Ser1099Ter)
18g.44953113C>TCA8945978SETBP1c.3773C>T (p.Ser1258Leu)
c.3851C>T (p.Ser1284Leu)
c.3296C>T (p.Ser1099Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953114A=CA2300141263SETBP1c.3774A= (p.Ser1258=)
c.3852A= (p.Ser1284=)
c.3297A= (p.Ser1099=)
18g.44953114A>CCA503982954SETBP1c.3774A>C (p.Ser1258=)
c.3852A>C (p.Ser1284=)
c.3297A>C (p.Ser1099=)
18g.44953114A>GCA503982955SETBP1c.3774A>G (p.Ser1258=)
c.3852A>G (p.Ser1284=)
c.3297A>G (p.Ser1099=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953114A>TCA503982956SETBP1c.3774A>T (p.Ser1258=)
c.3852A>T (p.Ser1284=)
c.3297A>T (p.Ser1099=)
 COSMIC
18g.44953115T>ACA402325162SETBP1c.3775T>A (p.Cys1259Ser)
c.3853T>A (p.Cys1285Ser)
c.3298T>A (p.Cys1100Ser)
 ClinVar dbSNP
18g.44953115T>CCA402325160SETBP1c.3775T>C (p.Cys1259Arg)
c.3853T>C (p.Cys1285Arg)
c.3298T>C (p.Cys1100Arg)
 dbSNP gnomAD v3 gnomAD v4
18g.44953115T>GCA402325161SETBP1c.3775T>G (p.Cys1259Gly)
c.3853T>G (p.Cys1285Gly)
c.3298T>G (p.Cys1100Gly)
18g.44953115T=CA2300141264SETBP1c.3775T= (p.Cys1259=)
c.3853T= (p.Cys1285=)
c.3298T= (p.Cys1100=)
18g.44953116G>ACA402325163SETBP1c.3776G>A (p.Cys1259Tyr)
c.3854G>A (p.Cys1285Tyr)
c.3299G>A (p.Cys1100Tyr)
18g.44953116G>CCA402325164SETBP1c.3776G>C (p.Cys1259Ser)
c.3854G>C (p.Cys1285Ser)
c.3299G>C (p.Cys1100Ser)
18g.44953116G=CA2300141265SETBP1c.3776G= (p.Cys1259=)
c.3854G= (p.Cys1285=)
c.3299G= (p.Cys1100=)
18g.44953116G>TCA402325165SETBP1c.3776G>T (p.Cys1259Phe)
c.3854G>T (p.Cys1285Phe)
c.3299G>T (p.Cys1100Phe)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953117C>ACA402325166SETBP1c.3777C>A (p.Cys1259Ter)
c.3855C>A (p.Cys1285Ter)
c.3300C>A (p.Cys1100Ter)
18g.44953117C>GCA402325167SETBP1c.3777C>G (p.Cys1259Trp)
c.3855C>G (p.Cys1285Trp)
c.3300C>G (p.Cys1100Trp)
18g.44953117C>TCA503982958SETBP1c.3777C>T (p.Cys1259=)
c.3855C>T (p.Cys1285=)
c.3300C>T (p.Cys1100=)
18g.44953118A>CCA402325168SETBP1c.3778A>C (p.Thr1260Pro)
c.3856A>C (p.Thr1286Pro)
c.3301A>C (p.Thr1101Pro)
18g.44953118A>GCA402325170SETBP1c.3778A>G (p.Thr1260Ala)
c.3856A>G (p.Thr1286Ala)
c.3301A>G (p.Thr1101Ala)
18g.44953118A>TCA402325169SETBP1c.3778A>T (p.Thr1260Ser)
c.3856A>T (p.Thr1286Ser)
c.3301A>T (p.Thr1101Ser)
18g.44953119C>ACA402325171SETBP1c.3779C>A (p.Thr1260Lys)
c.3857C>A (p.Thr1286Lys)
c.3302C>A (p.Thr1101Lys)
18g.44953119C=CA2300141266SETBP1c.3779C= (p.Thr1260=)
c.3857C= (p.Thr1286=)
c.3302C= (p.Thr1101=)
18g.44953119C>GCA402325172SETBP1c.3779C>G (p.Thr1260Arg)
c.3857C>G (p.Thr1286Arg)
c.3302C>G (p.Thr1101Arg)
 gnomAD v4
18g.44953119C>TCA8945979SETBP1c.3779C>T (p.Thr1260Met)
c.3857C>T (p.Thr1286Met)
c.3302C>T (p.Thr1101Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953120G>ACA8945980SETBP1c.3780G>A (p.Thr1260=)
c.3858G>A (p.Thr1286=)
c.3303G>A (p.Thr1101=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.44953120G>CCA503982959SETBP1c.3780G>C (p.Thr1260=)
c.3858G>C (p.Thr1286=)
c.3303G>C (p.Thr1101=)
18g.44953120G=CA2300141267SETBP1c.3780G= (p.Thr1260=)
c.3858G= (p.Thr1286=)
c.3303G= (p.Thr1101=)
18g.44953120G>TCA503982960SETBP1c.3780G>T (p.Thr1260=)
c.3858G>T (p.Thr1286=)
c.3303G>T (p.Thr1101=)
18g.44953121A>CCA402325173SETBP1c.3781A>C (p.Lys1261Gln)
c.3859A>C (p.Lys1287Gln)
c.3304A>C (p.Lys1102Gln)
18g.44953121A>GCA402325174SETBP1c.3781A>G (p.Lys1261Glu)
c.3859A>G (p.Lys1287Glu)
c.3304A>G (p.Lys1102Glu)
 COSMIC
18g.44953121A>TCA402325175SETBP1c.3781A>T (p.Lys1261Ter)
c.3859A>T (p.Lys1287Ter)
c.3304A>T (p.Lys1102Ter)
18g.44953122A=CA2300141268SETBP1c.3782A= (p.Lys1261=)
c.3860A= (p.Lys1287=)
c.3305A= (p.Lys1102=)
18g.44953122A>CCA402325176SETBP1c.3782A>C (p.Lys1261Thr)
c.3860A>C (p.Lys1287Thr)
c.3305A>C (p.Lys1102Thr)
18g.44953122A>GCA8945981SETBP1c.3782A>G (p.Lys1261Arg)
c.3860A>G (p.Lys1287Arg)
c.3305A>G (p.Lys1102Arg)
 dbSNP ExAC gnomAD v2
18g.44953122A>TCA402325177SETBP1c.3782A>T (p.Lys1261Ile)
c.3860A>T (p.Lys1287Ile)
c.3305A>T (p.Lys1102Ile)
 dbSNP
18g.44953123A>CCA402325178SETBP1c.3783A>C (p.Lys1261Asn)
c.3861A>C (p.Lys1287Asn)
c.3306A>C (p.Lys1102Asn)
18g.44953123A>GCA503982962SETBP1c.3783A>G (p.Lys1261=)
c.3861A>G (p.Lys1287=)
c.3306A>G (p.Lys1102=)
18g.44953123A>TCA402325179SETBP1c.3783A>T (p.Lys1261Asn)
c.3861A>T (p.Lys1287Asn)
c.3306A>T (p.Lys1102Asn)
18g.44953124A=CA2300141269SETBP1c.3784A= (p.Arg1262=)
c.3862A= (p.Arg1288=)
c.3307A= (p.Arg1103=)
18g.44953124A>CCA503982963SETBP1c.3784A>C (p.Arg1262=)
c.3862A>C (p.Arg1288=)
c.3307A>C (p.Arg1103=)
 dbSNP gnomAD v4
18g.44953124A>GCA402325180SETBP1c.3784A>G (p.Arg1262Gly)
c.3862A>G (p.Arg1288Gly)
c.3307A>G (p.Arg1103Gly)
18g.44953124A>TCA402325181SETBP1c.3784A>T (p.Arg1262Ter)
c.3862A>T (p.Arg1288Ter)
c.3307A>T (p.Arg1103Ter)
18g.44953125G>ACA402325182SETBP1c.3785G>A (p.Arg1262Lys)
c.3863G>A (p.Arg1288Lys)
c.3308G>A (p.Arg1103Lys)
18g.44953125G>CCA402325183SETBP1c.3785G>C (p.Arg1262Thr)
c.3863G>C (p.Arg1288Thr)
c.3308G>C (p.Arg1103Thr)
 COSMIC
18g.44953125G>TCA402325184SETBP1c.3785G>T (p.Arg1262Ile)
c.3863G>T (p.Arg1288Ile)
c.3308G>T (p.Arg1103Ile)
18g.44953126A>CCA402325185SETBP1c.3786A>C (p.Arg1262Ser)
c.3864A>C (p.Arg1288Ser)
c.3309A>C (p.Arg1103Ser)
18g.44953126A>GCA503982967SETBP1c.3786A>G (p.Arg1262=)
c.3864A>G (p.Arg1288=)
c.3309A>G (p.Arg1103=)
 ClinVar
18g.44953126A>TCA402325186SETBP1c.3786A>T (p.Arg1262Ser)
c.3864A>T (p.Arg1288Ser)
c.3309A>T (p.Arg1103Ser)
18g.44953127T>ACA402325187SETBP1c.3787T>A (p.Tyr1263Asn)
c.3865T>A (p.Tyr1289Asn)
c.3310T>A (p.Tyr1104Asn)
18g.44953127T>CCA402325188SETBP1c.3787T>C (p.Tyr1263His)
c.3865T>C (p.Tyr1289His)
c.3310T>C (p.Tyr1104His)
 gnomAD v4
18g.44953127T>GCA402325189SETBP1c.3787T>G (p.Tyr1263Asp)
c.3865T>G (p.Tyr1289Asp)
c.3310T>G (p.Tyr1104Asp)
18g.44953128A=CA2300141270SETBP1c.3788A= (p.Tyr1263=)
c.3866A= (p.Tyr1289=)
c.3311A= (p.Tyr1104=)
18g.44953128A>CCA402325190SETBP1c.3788A>C (p.Tyr1263Ser)
c.3866A>C (p.Tyr1289Ser)
c.3311A>C (p.Tyr1104Ser)
18g.44953128A>GCA299699782SETBP1c.3788A>G (p.Tyr1263Cys)
c.3866A>G (p.Tyr1289Cys)
c.3311A>G (p.Tyr1104Cys)
 dbSNP
18g.44953128A>TCA402325191SETBP1c.3788A>T (p.Tyr1263Phe)
c.3866A>T (p.Tyr1289Phe)
c.3311A>T (p.Tyr1104Phe)
18g.44953129C>ACA402325192SETBP1c.3789C>A (p.Tyr1263Ter)
c.3867C>A (p.Tyr1289Ter)
c.3312C>A (p.Tyr1104Ter)
 COSMIC
18g.44953129C>GCA402325193SETBP1c.3789C>G (p.Tyr1263Ter)
c.3867C>G (p.Tyr1289Ter)
c.3312C>G (p.Tyr1104Ter)
18g.44953129C>TCA503982972SETBP1c.3789C>T (p.Tyr1263=)
c.3867C>T (p.Tyr1289=)
c.3312C>T (p.Tyr1104=)
 ClinVar
18g.44953130T>ACA402325195SETBP1c.3790T>A (p.Ser1264Thr)
c.3868T>A (p.Ser1290Thr)
c.3313T>A (p.Ser1105Thr)
18g.44953130T>CCA402325194SETBP1c.3790T>C (p.Ser1264Pro)
c.3868T>C (p.Ser1290Pro)
c.3313T>C (p.Ser1105Pro)
 gnomAD v4
18g.44953130T>GCA8945982SETBP1c.3790T>G (p.Ser1264Ala)
c.3868T>G (p.Ser1290Ala)
c.3313T>G (p.Ser1105Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953130T=CA2300141271SETBP1c.3790T= (p.Ser1264=)
c.3868T= (p.Ser1290=)
c.3313T= (p.Ser1105=)
18g.44953131C>ACA402325196SETBP1c.3791C>A (p.Ser1264Tyr)
c.3869C>A (p.Ser1290Tyr)
c.3314C>A (p.Ser1105Tyr)
18g.44953131C>GCA402325197SETBP1c.3791C>G (p.Ser1264Cys)
c.3869C>G (p.Ser1290Cys)
c.3314C>G (p.Ser1105Cys)
18g.44953131C>TCA402325198SETBP1c.3791C>T (p.Ser1264Phe)
c.3869C>T (p.Ser1290Phe)
c.3314C>T (p.Ser1105Phe)
18g.44953132T>ACA503982976SETBP1c.3792T>A (p.Ser1264=)
c.3870T>A (p.Ser1290=)
c.3315T>A (p.Ser1105=)
18g.44953132T>CCA503982975SETBP1c.3792T>C (p.Ser1264=)
c.3870T>C (p.Ser1290=)
c.3315T>C (p.Ser1105=)
 gnomAD v4
18g.44953132T>GCA503982974SETBP1c.3792T>G (p.Ser1264=)
c.3870T>G (p.Ser1290=)
c.3315T>G (p.Ser1105=)
 COSMIC
18g.44953133G>ACA402325199SETBP1c.3793G>A (p.Gly1265Ser)
c.3871G>A (p.Gly1291Ser)
c.3316G>A (p.Gly1106Ser)
 dbSNP
18g.44953133G>CCA402325200SETBP1c.3793G>C (p.Gly1265Arg)
c.3871G>C (p.Gly1291Arg)
c.3316G>C (p.Gly1106Arg)
18g.44953133G=CA2300141272SETBP1c.3793G= (p.Gly1265=)
c.3871G= (p.Gly1291=)
c.3316G= (p.Gly1106=)
18g.44953133G>TCA402325201SETBP1c.3793G>T (p.Gly1265Cys)
c.3871G>T (p.Gly1291Cys)
c.3316G>T (p.Gly1106Cys)
18g.44953134G>ACA402325202SETBP1c.3794G>A (p.Gly1265Asp)
c.3872G>A (p.Gly1291Asp)
c.3317G>A (p.Gly1106Asp)
18g.44953134G>CCA402325203SETBP1c.3794G>C (p.Gly1265Ala)
c.3872G>C (p.Gly1291Ala)
c.3317G>C (p.Gly1106Ala)
18g.44953134G>TCA402325204SETBP1c.3794G>T (p.Gly1265Val)
c.3872G>T (p.Gly1291Val)
c.3317G>T (p.Gly1106Val)
18g.44953135C>ACA503982980SETBP1c.3795C>A (p.Gly1265=)
c.3873C>A (p.Gly1291=)
c.3318C>A (p.Gly1106=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953135C=CA2300141273SETBP1c.3795C= (p.Gly1265=)
c.3873C= (p.Gly1291=)
c.3318C= (p.Gly1106=)
18g.44953135C>GCA503982981SETBP1c.3795C>G (p.Gly1265=)
c.3873C>G (p.Gly1291=)
c.3318C>G (p.Gly1106=)
18g.44953135C>TCA503982982SETBP1c.3795C>T (p.Gly1265=)
c.3873C>T (p.Gly1291=)
c.3318C>T (p.Gly1106=)
18g.44953136A=CA2300141274SETBP1c.3796A= (p.Ser1266=)
c.3874A= (p.Ser1292=)
c.3319A= (p.Ser1107=)
18g.44953136A>CCA402325205SETBP1c.3796A>C (p.Ser1266Arg)
c.3874A>C (p.Ser1292Arg)
c.3319A>C (p.Ser1107Arg)
18g.44953136A>GCA402325206SETBP1c.3796A>G (p.Ser1266Gly)
c.3874A>G (p.Ser1292Gly)
c.3319A>G (p.Ser1107Gly)
18g.44953136A>TCA402325207SETBP1c.3796A>T (p.Ser1266Cys)
c.3874A>T (p.Ser1292Cys)
c.3319A>T (p.Ser1107Cys)
 ClinVar dbSNP gnomAD v4
18g.44953137G>ACA402325208SETBP1c.3797G>A (p.Ser1266Asn)
c.3875G>A (p.Ser1292Asn)
c.3320G>A (p.Ser1107Asn)
 ClinVar
18g.44953137G>CCA402325210SETBP1c.3797G>C (p.Ser1266Thr)
c.3875G>C (p.Ser1292Thr)
c.3320G>C (p.Ser1107Thr)
18g.44953137G>TCA402325209SETBP1c.3797G>T (p.Ser1266Ile)
c.3875G>T (p.Ser1292Ile)
c.3320G>T (p.Ser1107Ile)
18g.44953138T>ACA402325211SETBP1c.3798T>A (p.Ser1266Arg)
c.3876T>A (p.Ser1292Arg)
c.3321T>A (p.Ser1107Arg)
18g.44953138T>CCA503982986SETBP1c.3798T>C (p.Ser1266=)
c.3876T>C (p.Ser1292=)
c.3321T>C (p.Ser1107=)
18g.44953138T>GCA402325212SETBP1c.3798T>G (p.Ser1266Arg)
c.3876T>G (p.Ser1292Arg)
c.3321T>G (p.Ser1107Arg)
18g.44953139G>ACA402325213SETBP1c.3799G>A (p.Gly1267Ser)
c.3877G>A (p.Gly1293Ser)
c.3322G>A (p.Gly1108Ser)
 gnomAD v4
18g.44953139G>CCA402325214SETBP1c.3799G>C (p.Gly1267Arg)
c.3877G>C (p.Gly1293Arg)
c.3322G>C (p.Gly1108Arg)
18g.44953139G>TCA402325215SETBP1c.3799G>T (p.Gly1267Cys)
c.3877G>T (p.Gly1293Cys)
c.3322G>T (p.Gly1108Cys)
 ClinVar
18g.44953139_44953140insCCA2695227492SETBP1c.3799_3800insC (p.Gly1267AlafsTer17)
c.3877_3878insC (p.Gly1293AlafsTer17)
c.3322_3323insC (p.Gly1108AlafsTer17)
18g.44953140G>ACA402325216SETBP1c.3800G>A (p.Gly1267Asp)
c.3878G>A (p.Gly1293Asp)
c.3323G>A (p.Gly1108Asp)
 gnomAD v4
18g.44953140G>CCA402325217SETBP1c.3800G>C (p.Gly1267Ala)
c.3878G>C (p.Gly1293Ala)
c.3323G>C (p.Gly1108Ala)
18g.44953140G>TCA402325218SETBP1c.3800G>T (p.Gly1267Val)
c.3878G>T (p.Gly1293Val)
c.3323G>T (p.Gly1108Val)
18g.44953141C>ACA503982990SETBP1c.3801C>A (p.Gly1267=)
c.3879C>A (p.Gly1293=)
c.3324C>A (p.Gly1108=)
 dbSNP
18g.44953141C=CA2300141275SETBP1c.3801C= (p.Gly1267=)
c.3879C= (p.Gly1293=)
c.3324C= (p.Gly1108=)
18g.44953141C>GCA503982992SETBP1c.3801C>G (p.Gly1267=)
c.3879C>G (p.Gly1293=)
c.3324C>G (p.Gly1108=)
18g.44953141C>TCA8945983SETBP1c.3801C>T (p.Gly1267=)
c.3879C>T (p.Gly1293=)
c.3324C>T (p.Gly1108=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
18g.44953142G>ACA8945984SETBP1c.3802G>A (p.Gly1268Arg)
c.3880G>A (p.Gly1294Arg)
c.3325G>A (p.Gly1109Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953142G>CCA402325219SETBP1c.3802G>C (p.Gly1268Arg)
c.3880G>C (p.Gly1294Arg)
c.3325G>C (p.Gly1109Arg)
 gnomAD v4
18g.44953142G=CA2300141276SETBP1c.3802G= (p.Gly1268=)
c.3880G= (p.Gly1294=)
c.3325G= (p.Gly1109=)
18g.44953142G>TCA402325220SETBP1c.3802G>T (p.Gly1268Trp)
c.3880G>T (p.Gly1294Trp)
c.3325G>T (p.Gly1109Trp)
 ClinVar
18g.44953143G>ACA402325221SETBP1c.3803G>A (p.Gly1268Glu)
c.3881G>A (p.Gly1294Glu)
c.3326G>A (p.Gly1109Glu)
18g.44953143G>CCA402325222SETBP1c.3803G>C (p.Gly1268Ala)
c.3881G>C (p.Gly1294Ala)
c.3326G>C (p.Gly1109Ala)
18g.44953143G>TCA402325223SETBP1c.3803G>T (p.Gly1268Val)
c.3881G>T (p.Gly1294Val)
c.3326G>T (p.Gly1109Val)
18g.44953144G>ACA503982995SETBP1c.3804G>A (p.Gly1268=)
c.3882G>A (p.Gly1294=)
c.3327G>A (p.Gly1109=)
18g.44953144G>CCA503982996SETBP1c.3804G>C (p.Gly1268=)
c.3882G>C (p.Gly1294=)
c.3327G>C (p.Gly1109=)
 gnomAD v4
18g.44953144G>TCA503982998SETBP1c.3804G>T (p.Gly1268=)
c.3882G>T (p.Gly1294=)
c.3327G>T (p.Gly1109=)
18g.44953145G>ACA402325226SETBP1c.3805G>A (p.Asp1269Asn)
c.3883G>A (p.Asp1295Asn)
c.3328G>A (p.Asp1110Asn)
 dbSNP gnomAD v3 gnomAD v4
18g.44953145G>CCA402325225SETBP1c.3805G>C (p.Asp1269His)
c.3883G>C (p.Asp1295His)
c.3328G>C (p.Asp1110His)
18g.44953145G=CA2300141278SETBP1c.3805G= (p.Asp1269=)
c.3883G= (p.Asp1295=)
c.3328G= (p.Asp1110=)
18g.44953145G>TCA402325224SETBP1c.3805G>T (p.Asp1269Tyr)
c.3883G>T (p.Asp1295Tyr)
c.3328G>T (p.Asp1110Tyr)
18g.44953145_44953147delinsGATCA2300141277SETBP1c.3805_3807delinsGAT (p.Asp1269=)
c.3883_3885delinsGAT (p.Asp1295=)
c.3328_3330delinsGAT (p.Asp1110=)
18g.44953146_44953148delCA645613027SETBP1c.3806_3808del (p.Asp1269del)
c.3884_3886del (p.Asp1295del)
c.3329_3331del (p.Asp1110del)
 COSMIC
18g.44953146A=CA2300141279SETBP1c.3806A= (p.Asp1269=)
c.3884A= (p.Asp1295=)
c.3329A= (p.Asp1110=)
18g.44953146A>CCA402325227SETBP1c.3806A>C (p.Asp1269Ala)
c.3884A>C (p.Asp1295Ala)
c.3329A>C (p.Asp1110Ala)
18g.44953146A>GCA8945986SETBP1c.3806A>G (p.Asp1269Gly)
c.3884A>G (p.Asp1295Gly)
c.3329A>G (p.Asp1110Gly)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.44953146A>TCA8945987SETBP1c.3806A>T (p.Asp1269Val)
c.3884A>T (p.Asp1295Val)
c.3329A>T (p.Asp1110Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953146_44953147delCA8945985SETBP1c.3806_3807del (p.Asp1269GlyfsTer14)
c.3884_3885del (p.Asp1295GlyfsTer14)
c.3329_3330del (p.Asp1110GlyfsTer14)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953147T>ACA402325228SETBP1c.3807T>A (p.Asp1269Glu)
c.3885T>A (p.Asp1295Glu)
c.3330T>A (p.Asp1110Glu)
18g.44953147T>CCA503983002SETBP1c.3807T>C (p.Asp1269=)
c.3885T>C (p.Asp1295=)
c.3330T>C (p.Asp1110=)
18g.44953147T>GCA8945988SETBP1c.3807T>G (p.Asp1269Glu)
c.3885T>G (p.Asp1295Glu)
c.3330T>G (p.Asp1110Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953147T=CA2300141280SETBP1c.3807T= (p.Asp1269=)
c.3885T= (p.Asp1295=)
c.3330T= (p.Asp1110=)
18g.44953148G>ACA8945989SETBP1c.3808G>A (p.Gly1270Ser)
c.3886G>A (p.Gly1296Ser)
c.3331G>A (p.Gly1111Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953148G>CCA402325229SETBP1c.3808G>C (p.Gly1270Arg)
c.3886G>C (p.Gly1296Arg)
c.3331G>C (p.Gly1111Arg)
18g.44953148G=CA2300141281SETBP1c.3808G= (p.Gly1270=)
c.3886G= (p.Gly1296=)
c.3331G= (p.Gly1111=)
18g.44953148G>TCA402325230SETBP1c.3808G>T (p.Gly1270Cys)
c.3886G>T (p.Gly1296Cys)
c.3331G>T (p.Gly1111Cys)
 gnomAD v4
18g.44953149G>ACA402325231SETBP1c.3809G>A (p.Gly1270Asp)
c.3887G>A (p.Gly1296Asp)
c.3332G>A (p.Gly1111Asp)
 dbSNP gnomAD v2 gnomAD v4
18g.44953149G>CCA402325232SETBP1c.3809G>C (p.Gly1270Ala)
c.3887G>C (p.Gly1296Ala)
c.3332G>C (p.Gly1111Ala)
18g.44953149G=CA2300141282SETBP1c.3809G= (p.Gly1270=)
c.3887G= (p.Gly1296=)
c.3332G= (p.Gly1111=)
18g.44953149G>TCA402325233SETBP1c.3809G>T (p.Gly1270Val)
c.3887G>T (p.Gly1296Val)
c.3332G>T (p.Gly1111Val)
18g.44953150T>ACA503983004SETBP1c.3810T>A (p.Gly1270=)
c.3888T>A (p.Gly1296=)
c.3333T>A (p.Gly1111=)
18g.44953150T>CCA503983005SETBP1c.3810T>C (p.Gly1270=)
c.3888T>C (p.Gly1296=)
c.3333T>C (p.Gly1111=)
18g.44953150T>GCA8945990SETBP1c.3810T>G (p.Gly1270=)
c.3888T>G (p.Gly1296=)
c.3333T>G (p.Gly1111=)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953150T=CA2300141283SETBP1c.3810T= (p.Gly1270=)
c.3888T= (p.Gly1296=)
c.3333T= (p.Gly1111=)
18g.44953151G>ACA299699796SETBP1c.3811G>A (p.Gly1271Ser)
c.3889G>A (p.Gly1297Ser)
c.3334G>A (p.Gly1112Ser)
 dbSNP gnomAD v4
18g.44953151G>CCA402325235SETBP1c.3811G>C (p.Gly1271Arg)
c.3889G>C (p.Gly1297Arg)
c.3334G>C (p.Gly1112Arg)
18g.44953151G=CA2300141284SETBP1c.3811G= (p.Gly1271=)
c.3889G= (p.Gly1297=)
c.3334G= (p.Gly1112=)
18g.44953151G>TCA402325234SETBP1c.3811G>T (p.Gly1271Cys)
c.3889G>T (p.Gly1297Cys)
c.3334G>T (p.Gly1112Cys)
18g.44953152G>ACA402325236SETBP1c.3812G>A (p.Gly1271Asp)
c.3890G>A (p.Gly1297Asp)
c.3335G>A (p.Gly1112Asp)
18g.44953152G>CCA402325237SETBP1c.3812G>C (p.Gly1271Ala)
c.3890G>C (p.Gly1297Ala)
c.3335G>C (p.Gly1112Ala)
18g.44953152G>TCA402325238SETBP1c.3812G>T (p.Gly1271Val)
c.3890G>T (p.Gly1297Val)
c.3335G>T (p.Gly1112Val)
18g.44953153C>ACA503983010SETBP1c.3813C>A (p.Gly1271=)
c.3891C>A (p.Gly1297=)
c.3336C>A (p.Gly1112=)
18g.44953153C=CA2300141285SETBP1c.3813C= (p.Gly1271=)
c.3891C= (p.Gly1297=)
c.3336C= (p.Gly1112=)
18g.44953153C>GCA8945991SETBP1c.3813C>G (p.Gly1271=)
c.3891C>G (p.Gly1297=)
c.3336C>G (p.Gly1112=)
 dbSNP ExAC gnomAD v2
18g.44953153C>TCA503983011SETBP1c.3813C>T (p.Gly1271=)
c.3891C>T (p.Gly1297=)
c.3336C>T (p.Gly1112=)
18g.44953154A=CA2300141286SETBP1c.3814A= (p.Ser1272=)
c.3892A= (p.Ser1298=)
c.3337A= (p.Ser1113=)
18g.44953154A>CCA402325239SETBP1c.3814A>C (p.Ser1272Arg)
c.3892A>C (p.Ser1298Arg)
c.3337A>C (p.Ser1113Arg)
18g.44953154A>GCA402325240SETBP1c.3814A>G (p.Ser1272Gly)
c.3892A>G (p.Ser1298Gly)
c.3337A>G (p.Ser1113Gly)
 dbSNP gnomAD v2
18g.44953154A>TCA402325241SETBP1c.3814A>T (p.Ser1272Cys)
c.3892A>T (p.Ser1298Cys)
c.3337A>T (p.Ser1113Cys)
18g.44953155G>ACA402325242SETBP1c.3815G>A (p.Ser1272Asn)
c.3893G>A (p.Ser1298Asn)
c.3338G>A (p.Ser1113Asn)
 ClinVar gnomAD v4
18g.44953155G>CCA402325243SETBP1c.3815G>C (p.Ser1272Thr)
c.3893G>C (p.Ser1298Thr)
c.3338G>C (p.Ser1113Thr)
 COSMIC
18g.44953155G>TCA402325244SETBP1c.3815G>T (p.Ser1272Ile)
c.3893G>T (p.Ser1298Ile)
c.3338G>T (p.Ser1113Ile)
18g.44953156C>ACA402325245SETBP1c.3816C>A (p.Ser1272Arg)
c.3894C>A (p.Ser1298Arg)
c.3339C>A (p.Ser1113Arg)
18g.44953156C>GCA402325246SETBP1c.3816C>G (p.Ser1272Arg)
c.3894C>G (p.Ser1298Arg)
c.3339C>G (p.Ser1113Arg)
18g.44953156C>TCA503983013SETBP1c.3816C>T (p.Ser1272=)
c.3894C>T (p.Ser1298=)
c.3339C>T (p.Ser1113=)
18g.44953157A>CCA402325249SETBP1c.3817A>C (p.Thr1273Pro)
c.3895A>C (p.Thr1299Pro)
c.3340A>C (p.Thr1114Pro)
18g.44953157A>GCA402325247SETBP1c.3817A>G (p.Thr1273Ala)
c.3895A>G (p.Thr1299Ala)
c.3340A>G (p.Thr1114Ala)
18g.44953157A>TCA402325248SETBP1c.3817A>T (p.Thr1273Ser)
c.3895A>T (p.Thr1299Ser)
c.3340A>T (p.Thr1114Ser)
18g.44953158C>ACA402325250SETBP1c.3818C>A (p.Thr1273Lys)
c.3896C>A (p.Thr1299Lys)
c.3341C>A (p.Thr1114Lys)
 gnomAD v4
18g.44953158C=CA2300141287SETBP1c.3818C= (p.Thr1273=)
c.3896C= (p.Thr1299=)
c.3341C= (p.Thr1114=)
18g.44953158C>GCA402325251SETBP1c.3818C>G (p.Thr1273Arg)
c.3896C>G (p.Thr1299Arg)
c.3341C>G (p.Thr1114Arg)
 gnomAD v4
18g.44953158C>TCA299699816SETBP1c.3818C>T (p.Thr1273Met)
c.3896C>T (p.Thr1299Met)
c.3341C>T (p.Thr1114Met)
 ClinVar dbSNP gnomAD v2 gnomAD v4
18g.44953159G>ACA8945992SETBP1c.3819G>A (p.Thr1273=)
c.3897G>A (p.Thr1299=)
c.3342G>A (p.Thr1114=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953159G>CCA503983015SETBP1c.3819G>C (p.Thr1273=)
c.3897G>C (p.Thr1299=)
c.3342G>C (p.Thr1114=)
18g.44953159G=CA2300141288SETBP1c.3819G= (p.Thr1273=)
c.3897G= (p.Thr1299=)
c.3342G= (p.Thr1114=)
18g.44953159G>TCA503983016SETBP1c.3819G>T (p.Thr1273=)
c.3897G>T (p.Thr1299=)
c.3342G>T (p.Thr1114=)
18g.44953160A>CCA503983018SETBP1c.3820A>C (p.Arg1274=)
c.3898A>C (p.Arg1300=)
c.3343A>C (p.Arg1115=)
18g.44953160A>GCA402325252SETBP1c.3820A>G (p.Arg1274Gly)
c.3898A>G (p.Arg1300Gly)
c.3343A>G (p.Arg1115Gly)
18g.44953160A>TCA402325253SETBP1c.3820A>T (p.Arg1274Ter)
c.3898A>T (p.Arg1300Ter)
c.3343A>T (p.Arg1115Ter)
18g.44953161G>ACA402325254SETBP1c.3821G>A (p.Arg1274Lys)
c.3899G>A (p.Arg1300Lys)
c.3344G>A (p.Arg1115Lys)
18g.44953161G>CCA402325255SETBP1c.3821G>C (p.Arg1274Thr)
c.3899G>C (p.Arg1300Thr)
c.3344G>C (p.Arg1115Thr)
 gnomAD v4
18g.44953161G>TCA402325256SETBP1c.3821G>T (p.Arg1274Ile)
c.3899G>T (p.Arg1300Ile)
c.3344G>T (p.Arg1115Ile)
18g.44953162A=CA2300141289SETBP1c.3822A= (p.Arg1274=)
c.3900A= (p.Arg1300=)
c.3345A= (p.Arg1115=)
18g.44953162A>CCA402325257SETBP1c.3822A>C (p.Arg1274Ser)
c.3900A>C (p.Arg1300Ser)
c.3345A>C (p.Arg1115Ser)
18g.44953162A>GCA503983022SETBP1c.3822A>G (p.Arg1274=)
c.3900A>G (p.Arg1300=)
c.3345A>G (p.Arg1115=)
18g.44953162A>TCA402325258SETBP1c.3822A>T (p.Arg1274Ser)
c.3900A>T (p.Arg1300Ser)
c.3345A>T (p.Arg1115Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4
18g.44953163T>ACA402325260SETBP1c.3823T>A (p.Ser1275Thr)
c.3901T>A (p.Ser1301Thr)
c.3346T>A (p.Ser1116Thr)
18g.44953163T>CCA402325261SETBP1c.3823T>C (p.Ser1275Pro)
c.3901T>C (p.Ser1301Pro)
c.3346T>C (p.Ser1116Pro)
18g.44953163T>GCA402325259SETBP1c.3823T>G (p.Ser1275Ala)
c.3901T>G (p.Ser1301Ala)
c.3346T>G (p.Ser1116Ala)
18g.44953164C>ACA402325263SETBP1c.3824C>A (p.Ser1275Ter)
c.3902C>A (p.Ser1301Ter)
c.3347C>A (p.Ser1116Ter)
18g.44953164C=CA2300141290SETBP1c.3824C= (p.Ser1275=)
c.3902C= (p.Ser1301=)
c.3347C= (p.Ser1116=)
18g.44953164C>GCA402325262SETBP1c.3824C>G (p.Ser1275Ter)
c.3902C>G (p.Ser1301Ter)
c.3347C>G (p.Ser1116Ter)
18g.44953164C>TCA8945993SETBP1c.3824C>T (p.Ser1275Leu)
c.3902C>T (p.Ser1301Leu)
c.3347C>T (p.Ser1116Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953164_44953165delinsTGCA2573155232SETBP1c.3824_3825delinsTG (p.Ser1275Leu)
c.3902_3903delinsTG (p.Ser1301Leu)
c.3347_3348delinsTG (p.Ser1116Leu)
 ClinVar
18g.44953165A=CA2300141291SETBP1c.3825A= (p.Ser1275=)
c.3903A= (p.Ser1301=)
c.3348A= (p.Ser1116=)
18g.44953165A>CCA173396SETBP1c.3825A>C (p.Ser1275=)
c.3903A>C (p.Ser1301=)
c.3348A>C (p.Ser1116=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953165A>GCA173398SETBP1c.3825A>G (p.Ser1275=)
c.3903A>G (p.Ser1301=)
c.3348A>G (p.Ser1116=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953165A>TCA173399SETBP1c.3825A>T (p.Ser1275=)
c.3903A>T (p.Ser1301=)
c.3348A>T (p.Ser1116=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
18g.44953166G>ACA402325264SETBP1c.3826G>A (p.Glu1276Lys)
c.3904G>A (p.Glu1302Lys)
c.3349G>A (p.Glu1117Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953166G>CCA402325265SETBP1c.3826G>C (p.Glu1276Gln)
c.3904G>C (p.Glu1302Gln)
c.3349G>C (p.Glu1117Gln)
18g.44953166G=CA2300141292SETBP1c.3826G= (p.Glu1276=)
c.3904G= (p.Glu1302=)
c.3349G= (p.Glu1117=)
18g.44953166G>TCA402325266SETBP1c.3826G>T (p.Glu1276Ter)
c.3904G>T (p.Glu1302Ter)
c.3349G>T (p.Glu1117Ter)

Number of alleles fetched