Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.15191670G>CCA2576658933NOTCH3c.803-13C>G (n.803-13C>G)
c.800-13C>G (n.800-13C>G)
19g.15191672T>CCA2324749789NOTCH3c.803-15A>G (n.803-15A>G)
c.800-15A>G (n.800-15A>G)
dbSNP gnomAD v4
19g.15191672T>GCA9263777NOTCH3c.803-15A>C (n.803-15A>C)
c.800-15A>C (n.800-15A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.15191672T=CA2324749788NOTCH3c.803-15A= (n.803-15A=)
c.800-15A= (n.800-15A=)
19g.15191673G>CCA2735623989NOTCH3c.803-16C>G (n.803-16C>G)
c.800-16C>G (n.800-16C>G)
dbSNP
19g.15191673G=CA2324749790NOTCH3c.803-16C= (n.803-16C=)
c.800-16C= (n.800-16C=)
19g.15191673G>TCA9263778NOTCH3c.803-16C>A (n.803-16C>A)
c.800-16C>A (n.800-16C>A)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.15191674C>ACA2735623991NOTCH3c.803-17G>T (n.803-17G>T)
c.800-17G>T (n.800-17G>T)
dbSNP
19g.15191674C=CA2324749791NOTCH3c.803-17G= (n.803-17G=)
c.800-17G= (n.800-17G=)
19g.15191674C>GCA9263779NOTCH3c.803-17G>C (n.803-17G>C)
c.800-17G>C (n.800-17G>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.15191674C>TCA2735623990NOTCH3c.803-17G>A (n.803-17G>A)
c.800-17G>A (n.800-17G>A)
dbSNP
19g.15191676G>ACA2735784736NOTCH3c.803-19C>T (n.803-19C>T)
c.800-19C>T (n.800-19C>T)
dbSNP
19g.15191677C>ACA2735671187NOTCH3c.803-20G>T (n.803-20G>T)
c.800-20G>T (n.800-20G>T)
dbSNP
19g.15191677C=CA2324749792NOTCH3c.803-20G= (n.803-20G=)
c.800-20G= (n.800-20G=)
19g.15191677C>TCA2324749793NOTCH3c.803-20G>A (n.803-20G>A)
c.800-20G>A (n.800-20G>A)
dbSNP gnomAD v4
19g.15191679G>CCA2324749795NOTCH3c.803-22C>G (n.803-22C>G)
c.800-22C>G (n.800-22C>G)
dbSNP
19g.15191679G=CA2324749794NOTCH3c.803-22C= (n.803-22C=)
c.800-22C= (n.800-22C=)
19g.15191681C>ACA2583065559NOTCH3c.803-24G>T (n.803-24G>T)
c.800-24G>T (n.800-24G>T)
dbSNP gnomAD v4
19g.15191681C=CA2324749796NOTCH3c.803-24G= (n.803-24G=)
c.800-24G= (n.800-24G=)
19g.15191681C>GCA632128087NOTCH3c.803-24G>C (n.803-24G>C)
c.800-24G>C (n.800-24G>C)
dbSNP gnomAD v2 gnomAD v4
19g.15191682C>TCA2583065560NOTCH3c.803-25G>A (n.803-25G>A)
c.800-25G>A (n.800-25G>A)
dbSNP gnomAD v4
19g.15191685C>ACA2576658934NOTCH3c.803-28G>T (n.803-28G>T)
c.800-28G>T (n.800-28G>T)
dbSNP
19g.15191686C>ACA2735784844NOTCH3c.803-29G>T (n.803-29G>T)
c.800-29G>T (n.800-29G>T)
dbSNP
19g.15191686C>TCA2735784835NOTCH3c.803-29G>A (n.803-29G>A)
c.800-29G>A (n.800-29G>A)
dbSNP
19g.15191687A=CA2324749797NOTCH3c.803-30T= (n.803-30T=)
c.800-30T= (n.800-30T=)
19g.15191687A>GCA783621397NOTCH3c.803-30T>C (n.803-30T>C)
c.800-30T>C (n.800-30T>C)
dbSNP gnomAD v3 gnomAD v4
19g.15191687A>TCA2735638868NOTCH3c.803-30T>A (n.803-30T>A)
c.800-30T>A (n.800-30T>A)
dbSNP
19g.15191688C>ACA783621398NOTCH3c.803-31G>T (n.803-31G>T)
c.800-31G>T (n.800-31G>T)
dbSNP gnomAD v3 gnomAD v4
19g.15191688C=CA2324749798NOTCH3c.803-31G= (n.803-31G=)
c.800-31G= (n.800-31G=)
19g.15191688C>TCA632128088NOTCH3c.803-31G>A (n.803-31G>A)
c.800-31G>A (n.800-31G>A)
dbSNP gnomAD v2 gnomAD v4
19g.15191689C=CA2324749799NOTCH3c.803-32G= (n.803-32G=)
c.800-32G= (n.800-32G=)
19g.15191689C>GCA9263780NOTCH3c.803-32G>C (n.803-32G>C)
c.800-32G>C (n.800-32G>C)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.15191689C>TCA2735623371NOTCH3c.803-32G>A (n.803-32G>A)
c.800-32G>A (n.800-32G>A)
dbSNP
19g.15191690T>CCA2583065561NOTCH3c.803-33A>G (n.803-33A>G)
c.800-33A>G (n.800-33A>G)
gnomAD v4
19g.15191691G>ACA9263781NOTCH3c.803-34C>T (n.803-34C>T)
c.800-34C>T (n.800-34C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.15191691G=CA2324749800NOTCH3c.803-34C= (n.803-34C=)
c.800-34C= (n.800-34C=)
19g.15191691G>TCA2813728451NOTCH3c.803-34C>A (n.803-34C>A)
c.800-34C>A (n.800-34C>A)
19g.15191694_15191695delCA2813728452NOTCH3c.803-36_803-35del (n.803-36_803-35del)
c.800-36_800-35del (n.800-36_800-35del)
19g.15191693C=CA2324749801NOTCH3c.803-36G= (n.803-36G=)
c.800-36G= (n.800-36G=)
19g.15191693C>TCA632128089NOTCH3c.803-36G>A (n.803-36G>A)
c.800-36G>A (n.800-36G>A)
dbSNP gnomAD v2 gnomAD v4
19g.15191694G>ACA9263782NOTCH3c.803-37C>T (n.803-37C>T)
c.800-37C>T (n.800-37C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.15191694G=CA2324749802NOTCH3c.803-37C= (n.803-37C=)
c.800-37C= (n.800-37C=)
19g.15191694G>TCA2576658935NOTCH3c.803-37C>A (n.803-37C>A)
c.800-37C>A (n.800-37C>A)
gnomAD v4
19g.15191695_15191696insTTGGTAGAGATAGGGTTTTGCCCA2583065562NOTCH3c.803-38_803-37insGCAAAACCCTATCTCTACCAAG (n.803-38_803-37insGCAAAACCCTATCTCTACCAAG)
c.800-38_800-37insGCAAAACCCTATCTCTACCAAG (n.800-38_800-37insGCAAAACCCTATCTCTACCAAG)
gnomAD v4
19g.15191696A=CA2324749803NOTCH3c.803-39T= (n.803-39T=)
c.800-39T= (n.800-39T=)
19g.15191696A>GCA2324749804NOTCH3c.803-39T>C (n.803-39T>C)
c.800-39T>C (n.800-39T>C)
dbSNP gnomAD v4
19g.15191697T>ACA9263783NOTCH3c.803-40A>T (n.803-40A>T)
c.800-40A>T (n.800-40A>T)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.15191697T>CCA305777408NOTCH3c.803-40A>G (n.803-40A>G)
c.800-40A>G (n.800-40A>G)
dbSNP
19g.15191697T>GCA632128090NOTCH3c.803-40A>C (n.803-40A>C)
c.800-40A>C (n.800-40A>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.15191697T=CA2324749805NOTCH3c.803-40A= (n.803-40A=)
c.800-40A= (n.800-40A=)
19g.15191698G>ACA632128091NOTCH3c.803-41C>T (n.803-41C>T)
c.800-41C>T (n.800-41C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.15191698G=CA2324749806NOTCH3c.803-41C= (n.803-41C=)
c.800-41C= (n.800-41C=)
19g.15191699_15191700insTGCCCAGGCTCA2583065563NOTCH3c.803-42_803-41insGCCTGGGCAA (n.803-42_803-41insGCCTGGGCAA)
c.800-42_800-41insGCCTGGGCAA (n.800-42_800-41insGCCTGGGCAA)
gnomAD v4
19g.15191701C>TCA2735784848NOTCH3c.803-44G>A (n.803-44G>A)
c.800-44G>A (n.800-44G>A)
dbSNP
19g.15191702A=CA2324749807NOTCH3c.802+43T= (n.802+43T=)
c.799+43T= (n.799+43T=)
19g.15191702A>CCA2324749808NOTCH3c.802+43T>G (n.802+43T>G)
c.799+43T>G (n.799+43T>G)
dbSNP
19g.15191703C>ACA783621399NOTCH3c.802+42G>T (n.802+42G>T)
c.799+42G>T (n.799+42G>T)
dbSNP
19g.15191703C=CA2324749809NOTCH3c.802+42G= (n.802+42G=)
c.799+42G= (n.799+42G=)
19g.15191703C>TCA9263784NOTCH3c.802+42G>A (n.802+42G>A)
c.799+42G>A (n.799+42G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.15191705C=CA2324749810NOTCH3c.802+40G= (n.802+40G=)
c.799+40G= (n.799+40G=)
19g.15191705C>TCA632128092NOTCH3c.802+40G>A (n.802+40G>A)
c.799+40G>A (n.799+40G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.15191706G>ACA9263785NOTCH3c.802+39C>T (n.802+39C>T)
c.799+39C>T (n.799+39C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.15191706G>CCA2735623119NOTCH3c.802+39C>G (n.802+39C>G)
c.799+39C>G (n.799+39C>G)
dbSNP
19g.15191706G=CA2324749811NOTCH3c.802+39C= (n.802+39C=)
c.799+39C= (n.799+39C=)
19g.15191707A>TCA2735784856NOTCH3c.802+38T>A (n.802+38T>A)
c.799+38T>A (n.799+38T>A)
dbSNP
19g.15191708G>CCA632128093NOTCH3c.802+37C>G (n.802+37C>G)
c.799+37C>G (n.799+37C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.15191708G=CA2324749812NOTCH3c.802+37C= (n.802+37C=)
c.799+37C= (n.799+37C=)
19g.15191708G>TCA9263786NOTCH3c.802+37C>A (n.802+37C>A)
c.799+37C>A (n.799+37C>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.15191709G>CCA2735784886NOTCH3c.802+36C>G (n.802+36C>G)
c.799+36C>G (n.799+36C>G)
dbSNP
19g.15191710C>ACA305777430NOTCH3c.802+35G>T (n.802+35G>T)
c.799+35G>T (n.799+35G>T)
dbSNP gnomAD v2 gnomAD v4
19g.15191710C=CA2324749813NOTCH3c.802+35G= (n.802+35G=)
c.799+35G= (n.799+35G=)
19g.15191710C>GCA2583065564NOTCH3c.802+35G>C (n.802+35G>C)
c.799+35G>C (n.799+35G>C)
gnomAD v4
19g.15191710C>TCA2735633881NOTCH3c.802+35G>A (n.802+35G>A)
c.799+35G>A (n.799+35G>A)
dbSNP
19g.15191711C>TCA2735784898NOTCH3c.802+34G>A (n.802+34G>A)
c.799+34G>A (n.799+34G>A)
dbSNP
19g.15191712T>GCA2583065565NOTCH3c.802+33A>C (n.802+33A>C)
c.799+33A>C (n.799+33A>C)
gnomAD v4
19g.15191713G>ACA2735784933NOTCH3c.802+32C>T (n.802+32C>T)
c.799+32C>T (n.799+32C>T)
dbSNP
19g.15191714C>ACA2583065566NOTCH3c.802+31G>T (n.802+31G>T)
c.799+31G>T (n.799+31G>T)
dbSNP gnomAD v4
19g.15191714C=CA2324749814NOTCH3c.802+31G= (n.802+31G=)
c.799+31G= (n.799+31G=)
19g.15191714C>GCA2735650051NOTCH3c.802+31G>C (n.802+31G>C)
c.799+31G>C (n.799+31G>C)
dbSNP
19g.15191714C>TCA632128094NOTCH3c.802+31G>A (n.802+31G>A)
c.799+31G>A (n.799+31G>A)
dbSNP gnomAD v2 gnomAD v4
19g.15191715C>ACA2735784945NOTCH3c.802+30G>T (n.802+30G>T)
c.799+30G>T (n.799+30G>T)
dbSNP
19g.15191717C>ACA2813728453NOTCH3c.802+28G>T (n.802+28G>T)
c.799+28G>T (n.799+28G>T)
19g.15191717C>GCA2583065567NOTCH3c.802+28G>C (n.802+28G>C)
c.799+28G>C (n.799+28G>C)
gnomAD v4
19g.15191718C>TCA2735784949NOTCH3c.802+27G>A (n.802+27G>A)
c.799+27G>A (n.799+27G>A)
dbSNP
19g.15191720C>ACA2735619896NOTCH3c.802+25G>T (n.802+25G>T)
c.799+25G>T (n.799+25G>T)
dbSNP
19g.15191720C=CA2324749815NOTCH3c.802+25G= (n.802+25G=)
c.799+25G= (n.799+25G=)
19g.15191720C>TCA9263787NOTCH3c.802+25G>A (n.802+25G>A)
c.799+25G>A (n.799+25G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.15191721G>ACA9263788NOTCH3c.802+24C>T (n.802+24C>T)
c.799+24C>T (n.799+24C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.15191721G>CCA2735622787NOTCH3c.802+24C>G (n.802+24C>G)
c.799+24C>G (n.799+24C>G)
dbSNP
19g.15191721G=CA2324749816NOTCH3c.802+24C= (n.802+24C=)
c.799+24C= (n.799+24C=)
19g.15191722C=CA2324749817NOTCH3c.802+23G= (n.802+23G=)
c.799+23G= (n.799+23G=)
19g.15191722C>TCA9263789NOTCH3c.802+23G>A (n.802+23G>A)
c.799+23G>A (n.799+23G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.15191725C>TCA2583065568NOTCH3c.802+20G>A (n.802+20G>A)
c.799+20G>A (n.799+20G>A)
dbSNP gnomAD v4
19g.15191726C=CA2324749818NOTCH3c.802+19G= (n.802+19G=)
c.799+19G= (n.799+19G=)
19g.15191726C>GCA783621400NOTCH3c.802+19G>C (n.802+19G>C)
c.799+19G>C (n.799+19G>C)
dbSNP gnomAD v3 gnomAD v4
19g.15191728C>ACA2735784950NOTCH3c.802+17G>T (n.802+17G>T)
c.799+17G>T (n.799+17G>T)
dbSNP
19g.15191731G>CCA632128095NOTCH3c.802+14C>G (n.802+14C>G)
c.799+14C>G (n.799+14C>G)
dbSNP gnomAD v2 gnomAD v4
19g.15191731G=CA2324749819NOTCH3c.802+14C= (n.802+14C=)
c.799+14C= (n.799+14C=)
19g.15191731G>TCA2576658936NOTCH3c.802+14C>A (n.802+14C>A)
c.799+14C>A (n.799+14C>A)
19g.15191732C>TCA2735784966NOTCH3c.802+13G>A (n.802+13G>A)
c.799+13G>A (n.799+13G>A)
dbSNP
19g.15191733C=CA2324749820NOTCH3c.802+12G= (n.802+12G=)
c.799+12G= (n.799+12G=)
19g.15191733C>TCA9263790NOTCH3c.802+12G>A (n.802+12G>A)
c.799+12G>A (n.799+12G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.15191734G>ACA632128096NOTCH3c.802+11C>T (n.802+11C>T)
c.799+11C>T (n.799+11C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.15191734G>CCA2735637608NOTCH3c.802+11C>G (n.802+11C>G)
c.799+11C>G (n.799+11C>G)
dbSNP
19g.15191734G=CA2324749821NOTCH3c.802+11C= (n.802+11C=)
c.799+11C= (n.799+11C=)
19g.15191734G>TCA2813728454NOTCH3c.802+11C>A (n.802+11C>A)
c.799+11C>A (n.799+11C>A)
19g.15191734_15191735delinsGCCA2324749822NOTCH3c.802+10_802+11delinsGC (n.802+10_802+11delinsGC)
c.799+10_799+11delinsGC (n.799+10_799+11delinsGC)
19g.15191735delCA2324749823NOTCH3c.802+10del (n.802+10del)
c.799+10del (n.799+10del)
dbSNP
19g.15191736A>GCA2735784970NOTCH3c.802+9T>C (n.802+9T>C)
c.799+9T>C (n.799+9T>C)
dbSNP
19g.15191736dupCA2583065570NOTCH3c.802+9dup (n.802+9dup)
c.799+9dup (n.799+9dup)
gnomAD v4
19g.15191737G>ACA2735784975NOTCH3c.802+8C>T (n.802+8C>T)
c.799+8C>T (n.799+8C>T)
dbSNP
19g.15191738T>GCA2583065571NOTCH3c.802+7A>C (n.802+7A>C)
c.799+7A>C (n.799+7A>C)
gnomAD v4
19g.15191739G>ACA2735671190NOTCH3c.802+6C>T (n.802+6C>T)
c.799+6C>T (n.799+6C>T)
dbSNP
19g.15191739G>CCA993898900NOTCH3c.802+6C>G (n.802+6C>G)
c.799+6C>G (n.799+6C>G)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.15191739G=CA2324749824NOTCH3c.802+6C= (n.802+6C=)
c.799+6C= (n.799+6C=)
19g.15191740C=CA2324749825NOTCH3c.802+5G= (n.802+5G=)
c.799+5G= (n.799+5G=)
19g.15191740C>TCA783621401NOTCH3c.802+5G>A (n.802+5G>A)
c.799+5G>A (n.799+5G>A)
dbSNP gnomAD v3 gnomAD v4
19g.15191741C=CA2324749826NOTCH3c.802+4G= (n.802+4G=)
c.799+4G= (n.799+4G=)
19g.15191741C>TCA9263791NOTCH3c.802+4G>A (n.802+4G>A)
c.799+4G>A (n.799+4G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.15191742C>ACA2735784992NOTCH3c.802+3G>T (n.802+3G>T)
c.799+3G>T (n.799+3G>T)
dbSNP
19g.15191742C>TCA2576658937NOTCH3c.802+3G>A (n.802+3G>A)
c.799+3G>A (n.799+3G>A)
gnomAD v4
19g.15191743A=CA2324749827NOTCH3c.802+2T= (n.802+2T=)
c.799+2T= (n.799+2T=)
19g.15191743A>CCA404532081NOTCH3c.802+2T>G (n.802+2T>G)
c.799+2T>G (n.799+2T>G)
dbSNP gnomAD v4
19g.15191743A>GCA404532086NOTCH3c.802+2T>C (n.802+2T>C)
c.799+2T>C (n.799+2T>C)
19g.15191743A>TCA404532089NOTCH3c.802+2T>A (n.802+2T>A)
c.799+2T>A (n.799+2T>A)
dbSNP
19g.15191744C>ACA404532092NOTCH3c.802+1G>T (n.802+1G>T)
c.799+1G>T (n.799+1G>T)
19g.15191744C>GCA404532094NOTCH3c.802+1G>C (n.802+1G>C)
c.799+1G>C (n.799+1G>C)
19g.15191744C>TCA404532099NOTCH3c.802+1G>A (n.802+1G>A)
c.799+1G>A (n.799+1G>A)
dbSNP
19g.15191745C>ACA404532104NOTCH3c.802G>T (p.Gly268Cys)
c.799G>T (p.Gly267Cys)
19g.15191745C>GCA404532105NOTCH3c.802G>C (p.Gly268Arg)
c.799G>C (p.Gly267Arg)
dbSNP
19g.15191745C>TCA404532109NOTCH3c.802G>A (p.Gly268Ser)
c.799G>A (p.Gly267Ser)
19g.15191746T>ACA506078679NOTCH3c.801A>T (p.Thr267=)
c.798A>T (p.Thr266=)
19g.15191746T>CCA506078680NOTCH3c.801A>G (p.Thr267=)
c.798A>G (p.Thr266=)
19g.15191746T>GCA506078681NOTCH3c.801A>C (p.Thr267=)
c.798A>C (p.Thr266=)
19g.15191747G>ACA9263792NOTCH3c.800C>T (p.Thr267Ile)
c.797C>T (p.Thr266Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.15191747G>CCA404532113NOTCH3c.800C>G (p.Thr267Arg)
c.797C>G (p.Thr266Arg)
19g.15191747G=CA2324749828NOTCH3c.800C= (p.Thr267=)
c.797C= (p.Thr266=)
19g.15191747G>TCA404532119NOTCH3c.800C>A (p.Thr267Lys)
c.797C>A (p.Thr266Lys)
19g.15191748T>ACA404532121NOTCH3c.799A>T (p.Thr267Ser)
c.796A>T (p.Thr266Ser)
19g.15191748T>CCA404532122NOTCH3c.799A>G (p.Thr267Ala)
c.796A>G (p.Thr266Ala)
19g.15191748T>GCA404532124NOTCH3c.799A>C (p.Thr267Pro)
c.796A>C (p.Thr266Pro)
19g.15191749C>ACA404532127NOTCH3c.798G>T (p.Trp266Cys)
c.795G>T (p.Trp265Cys)
ClinVar dbSNP gnomAD v4
19g.15191749C=CA2324749829NOTCH3c.798G= (p.Trp266=)
c.795G= (p.Trp265=)
19g.15191749C>GCA404532130NOTCH3c.798G>C (p.Trp266Cys)
c.795G>C (p.Trp265Cys)
19g.15191749C>TCA404532134NOTCH3c.798G>A (p.Trp266Ter)
c.795G>A (p.Trp265Ter)
19g.15191750C>ACA404532138NOTCH3c.797G>T (p.Trp266Leu)
c.794G>T (p.Trp265Leu)
19g.15191750C>GCA404532139NOTCH3c.797G>C (p.Trp266Ser)
c.794G>C (p.Trp265Ser)
19g.15191750C>TCA404532144NOTCH3c.797G>A (p.Trp266Ter)
c.794G>A (p.Trp265Ter)
dbSNP COSMIC COSMIC
19g.15191751A>CCA404532146NOTCH3c.796T>G (p.Trp266Gly)
c.793T>G (p.Trp265Gly)
19g.15191751A>GCA404532151NOTCH3c.796T>C (p.Trp266Arg)
c.793T>C (p.Trp265Arg)
19g.15191751A>TCA404532160NOTCH3c.796T>A (p.Trp266Arg)
c.793T>A (p.Trp265Arg)
19g.15191752C>ACA404532162NOTCH3c.795G>T (p.Glu265Asp)
c.792G>T (p.Glu264Asp)
19g.15191752C>GCA404532161NOTCH3c.795G>C (p.Glu265Asp)
c.792G>C (p.Glu264Asp)
19g.15191752C>TCA506078686NOTCH3c.795G>A (p.Glu265=)
c.792G>A (p.Glu264=)
dbSNP
19g.15191753T>ACA404532165NOTCH3c.794A>T (p.Glu265Val)
c.791A>T (p.Glu264Val)
dbSNP
19g.15191753T>CCA404532180NOTCH3c.794A>G (p.Glu265Gly)
c.791A>G (p.Glu264Gly)
19g.15191753T>GCA404532182NOTCH3c.794A>C (p.Glu265Ala)
c.791A>C (p.Glu264Ala)
19g.15191754C>ACA404532187NOTCH3c.793G>T (p.Glu265Ter)
c.790G>T (p.Glu264Ter)
19g.15191754C=CA2324749830NOTCH3c.793G= (p.Glu265=)
c.790G= (p.Glu264=)
19g.15191754C>GCA404532190NOTCH3c.793G>C (p.Glu265Gln)
c.790G>C (p.Glu264Gln)
19g.15191754C>TCA404532193NOTCH3c.793G>A (p.Glu265Lys)
c.790G>A (p.Glu264Lys)
dbSNP
19g.15191755A>CCA506078689NOTCH3c.792T>G (p.Pro264=)
c.789T>G (p.Pro263=)
19g.15191755A>GCA506078690NOTCH3c.792T>C (p.Pro264=)
c.789T>C (p.Pro263=)
19g.15191755A>TCA506078691NOTCH3c.792T>A (p.Pro264=)
c.789T>A (p.Pro263=)
19g.15191756G>ACA404532205NOTCH3c.791C>T (p.Pro264Leu)
c.788C>T (p.Pro263Leu)
dbSNP
19g.15191756G>CCA404532202NOTCH3c.791C>G (p.Pro264Arg)
c.788C>G (p.Pro263Arg)
19g.15191756G>TCA404532201NOTCH3c.791C>A (p.Pro264His)
c.788C>A (p.Pro263His)
gnomAD v4
19g.15191757G>ACA9263793NOTCH3c.790C>T (p.Pro264Ser)
c.787C>T (p.Pro263Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.15191757G>CCA404532208NOTCH3c.790C>G (p.Pro264Ala)
c.787C>G (p.Pro263Ala)
19g.15191757G=CA2324749831NOTCH3c.790C= (p.Pro264=)
c.787C= (p.Pro263=)
19g.15191757G>TCA404532209NOTCH3c.790C>A (p.Pro264Thr)
c.787C>A (p.Pro263Thr)
COSMIC COSMIC COSMIC
19g.15191758A>CCA506078693NOTCH3c.789T>G (p.Pro263=)
c.786T>G (p.Pro262=)
19g.15191758A>GCA506078694NOTCH3c.789T>C (p.Pro263=)
c.786T>C (p.Pro262=)
19g.15191758A>TCA506078695NOTCH3c.789T>A (p.Pro263=)
c.786T>A (p.Pro262=)
19g.15191759G>ACA404532212NOTCH3c.788C>T (p.Pro263Leu)
c.785C>T (p.Pro262Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.15191759G>CCA404532215NOTCH3c.788C>G (p.Pro263Arg)
c.785C>G (p.Pro262Arg)
19g.15191759G=CA2324749832NOTCH3c.788C= (p.Pro263=)
c.785C= (p.Pro262=)
19g.15191759G>TCA404532216NOTCH3c.788C>A (p.Pro263His)
c.785C>A (p.Pro262His)
19g.15191760G>ACA404532220NOTCH3c.787C>T (p.Pro263Ser)
c.784C>T (p.Pro262Ser)
19g.15191760G>CCA404532223NOTCH3c.787C>G (p.Pro263Ala)
c.784C>G (p.Pro262Ala)
dbSNP
19g.15191760G>TCA404532221NOTCH3c.787C>A (p.Pro263Thr)
c.784C>A (p.Pro262Thr)
19g.15191761G>ACA9263794NOTCH3c.786C>T (p.Cys262=)
c.783C>T (p.Cys261=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.15191761G>CCA404532227NOTCH3c.786C>G (p.Cys262Trp)
c.783C>G (p.Cys261Trp)
19g.15191761G=CA2324749833NOTCH3c.786C= (p.Cys262=)
c.783C= (p.Cys261=)
19g.15191761G>TCA404532229NOTCH3c.786C>A (p.Cys262Ter)
c.783C>A (p.Cys261Ter)
19g.15191762C>ACA404532235NOTCH3c.785G>T (p.Cys262Phe)
c.782G>T (p.Cys261Phe)
19g.15191762C>GCA404532238NOTCH3c.785G>C (p.Cys262Ser)
c.782G>C (p.Cys261Ser)
19g.15191762C>TCA404532240NOTCH3c.785G>A (p.Cys262Tyr)
c.782G>A (p.Cys261Tyr)
19g.15191763A>CCA404532241NOTCH3c.784T>G (p.Cys262Gly)
c.781T>G (p.Cys261Gly)
19g.15191763A>GCA404532242NOTCH3c.784T>C (p.Cys262Arg)
c.781T>C (p.Cys261Arg)
gnomAD v4
19g.15191763A>TCA404532243NOTCH3c.784T>A (p.Cys262Ser)
c.781T>A (p.Cys261Ser)
19g.15191764C>ACA404532247NOTCH3c.783G>T (p.Gln261His)
c.780G>T (p.Gln260His)
19g.15191764C=CA2324749834NOTCH3c.783G= (p.Gln261=)
c.780G= (p.Gln260=)
19g.15191764C>GCA404532248NOTCH3c.783G>C (p.Gln261His)
c.780G>C (p.Gln260His)
19g.15191764C>TCA506078698NOTCH3c.783G>A (p.Gln261=)
c.780G>A (p.Gln260=)
dbSNP gnomAD v2 gnomAD v4
19g.15191765T>ACA404532250NOTCH3c.782A>T (p.Gln261Leu)
c.779A>T (p.Gln260Leu)
dbSNP
19g.15191765T>CCA404532254NOTCH3c.782A>G (p.Gln261Arg)
c.779A>G (p.Gln260Arg)
19g.15191765T>GCA404532252NOTCH3c.782A>C (p.Gln261Pro)
c.779A>C (p.Gln260Pro)
19g.15191766G>ACA404532257NOTCH3c.781C>T (p.Gln261Ter)
c.778C>T (p.Gln260Ter)
19g.15191766G>CCA404532265NOTCH3c.781C>G (p.Gln261Glu)
c.778C>G (p.Gln260Glu)
19g.15191766G>TCA404532259NOTCH3c.781C>A (p.Gln261Lys)
c.778C>A (p.Gln260Lys)
dbSNP
19g.15191767delCA2735785247NOTCH3c.781del (p.Gln261SerfsTer?)
c.778del (p.Gln260SerfsTer?)
dbSNP
19g.15191767G>ACA506078702NOTCH3c.780C>T (p.Cys260=)
c.777C>T (p.Cys259=)
dbSNP
19g.15191767G>CCA404532268NOTCH3c.780C>G (p.Cys260Trp)
c.777C>G (p.Cys259Trp)
dbSNP
19g.15191767G>TCA404532270NOTCH3c.780C>A (p.Cys260Ter)
c.777C>A (p.Cys259Ter)
19g.15191768C>ACA404532276NOTCH3c.779G>T (p.Cys260Phe)
c.776G>T (p.Cys259Phe)
ClinVar dbSNP
19g.15191768C=CA2324749835NOTCH3c.779G= (p.Cys260=)
c.776G= (p.Cys259=)
19g.15191768C>GCA404532280NOTCH3c.779G>C (p.Cys260Ser)
c.776G>C (p.Cys259Ser)
19g.15191768C>TCA404532284NOTCH3c.779G>A (p.Cys260Tyr)
c.776G>A (p.Cys259Tyr)
dbSNP
19g.15191769A>CCA404532286NOTCH3c.778T>G (p.Cys260Gly)
c.775T>G (p.Cys259Gly)
19g.15191769A>GCA404532287NOTCH3c.778T>C (p.Cys260Arg)
c.775T>C (p.Cys259Arg)
19g.15191769A>TCA404532292NOTCH3c.778T>A (p.Cys260Ser)
c.775T>A (p.Cys259Ser)
19g.15191770G>ACA506078707NOTCH3c.777C>T (p.Asn259=)
c.774C>T (p.Asn258=)
dbSNP gnomAD v4
19g.15191770G>CCA404532295NOTCH3c.777C>G (p.Asn259Lys)
c.774C>G (p.Asn258Lys)
gnomAD v4
19g.15191770G>TCA404532297NOTCH3c.777C>A (p.Asn259Lys)
c.774C>A (p.Asn258Lys)

Number of alleles fetched