Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154966555T>ACA414916572F8c.1142A>T (p.Asp381Val)
c.*1018A>T (n.*1018A>T)
c.1037A>T (p.Asp346Val)
Xg.154966555T>CCA414916574F8c.1142A>G (p.Asp381Gly)
c.*1018A>G (n.*1018A>G)
c.1037A>G (p.Asp346Gly)
Xg.154966555T>GCA414916582F8c.1142A>C (p.Asp381Ala)
c.*1018A>C (n.*1018A>C)
c.1037A>C (p.Asp346Ala)
Xg.154966556C>ACA414916587F8c.1141G>T (p.Asp381Tyr)
c.*1017G>T (n.*1017G>T)
c.1036G>T (p.Asp346Tyr)
Xg.154966556C>GCA414916592F8c.1141G>C (p.Asp381His)
c.*1017G>C (n.*1017G>C)
c.1036G>C (p.Asp346His)
Xg.154966556C>TCA414916589F8c.1141G>A (p.Asp381Asn)
c.*1017G>A (n.*1017G>A)
c.1036G>A (p.Asp346Asn)
COSMIC COSMIC
Xg.154966557A=CA2466848127F8c.1140T= (p.Asp380=)
c.*1016T= (n.*1016T=)
c.1035T= (p.Asp345=)
Xg.154966557A>CCA414916595F8c.1140T>G (p.Asp380Glu)
c.*1016T>G (n.*1016T>G)
c.1035T>G (p.Asp345Glu)
Xg.154966557A>GCA519365243F8c.1140T>C (p.Asp380=)
c.*1016T>C (n.*1016T>C)
c.1035T>C (p.Asp345=)
dbSNP
Xg.154966557A>TCA414916598F8c.1140T>A (p.Asp380Glu)
c.*1016T>A (n.*1016T>A)
c.1035T>A (p.Asp345Glu)
Xg.154966558T>ACA414916601F8c.1139A>T (p.Asp380Val)
c.*1015A>T (n.*1015A>T)
c.1034A>T (p.Asp345Val)
Xg.154966558T>CCA10568496F8c.1139A>G (p.Asp380Gly)
c.*1015A>G (n.*1015A>G)
c.1034A>G (p.Asp345Gly)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154966558T>GCA414916606F8c.1139A>C (p.Asp380Ala)
c.*1015A>C (n.*1015A>C)
c.1034A>C (p.Asp345Ala)
Xg.154966558T=CA2466848128F8c.1139A= (p.Asp380=)
c.*1015A= (n.*1015A=)
c.1034A= (p.Asp345=)
Xg.154966559C>ACA414916609F8c.1138G>T (p.Asp380Tyr)
c.*1014G>T (n.*1014G>T)
c.1033G>T (p.Asp345Tyr)
Xg.154966559C=CA2466848129F8c.1138G= (p.Asp380=)
c.*1014G= (n.*1014G=)
c.1033G= (p.Asp345=)
Xg.154966559C>GCA414916615F8c.1138G>C (p.Asp380His)
c.*1014G>C (n.*1014G>C)
c.1033G>C (p.Asp345His)
Xg.154966559C>TCA10568497F8c.1138G>A (p.Asp380Asn)
c.*1014G>A (n.*1014G>A)
c.1033G>A (p.Asp345Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154966561_154966572delCA2695237371F8c.1127_1138del (p.Val376_Phe379del)
c.*1003_*1014del (n.*1003_*1014del)
c.1022_1033del (p.Val341_Phe344del)
Xg.154966560A=CA2466848130F8c.1137T= (p.Phe379=)
c.*1013T= (n.*1013T=)
c.1032T= (p.Phe344=)
Xg.154966560A>CCA414916618F8c.1137T>G (p.Phe379Leu)
c.*1013T>G (n.*1013T>G)
c.1032T>G (p.Phe344Leu)
Xg.154966560A>GCA519365361F8c.1137T>C (p.Phe379=)
c.*1013T>C (n.*1013T>C)
c.1032T>C (p.Phe344=)
dbSNP gnomAD v2 gnomAD v4
Xg.154966560A>TCA414916620F8c.1137T>A (p.Phe379Leu)
c.*1013T>A (n.*1013T>A)
c.1032T>A (p.Phe344Leu)
Xg.154966561A>CCA414916624F8c.1136T>G (p.Phe379Cys)
c.*1012T>G (n.*1012T>G)
c.1031T>G (p.Phe344Cys)
gnomAD v4
Xg.154966561A>GCA414916629F8c.1136T>C (p.Phe379Ser)
c.*1012T>C (n.*1012T>C)
c.1031T>C (p.Phe344Ser)
Xg.154966561A>TCA414916626F8c.1136T>A (p.Phe379Tyr)
c.*1012T>A (n.*1012T>A)
c.1031T>A (p.Phe344Tyr)
Xg.154966562A>CCA414916631F8c.1135T>G (p.Phe379Val)
c.*1011T>G (n.*1011T>G)
c.1030T>G (p.Phe344Val)
Xg.154966562A>GCA414916634F8c.1135T>C (p.Phe379Leu)
c.*1011T>C (n.*1011T>C)
c.1030T>C (p.Phe344Leu)
Xg.154966562A>TCA414916635F8c.1135T>A (p.Phe379Ile)
c.*1011T>A (n.*1011T>A)
c.1030T>A (p.Phe344Ile)
Xg.154966562_154966563delinsACCA2466848131F8c.1134_1135delinsGT (p.Arg378=)
c.*1010_*1011delinsGT (n.*1010_*1011delinsGT)
c.1029_1030delinsGT (p.Arg343=)
Xg.154966563C>ACA10568499F8c.1134G>T (p.Arg378Ser)
c.*1010G>T (n.*1010G>T)
c.1029G>T (p.Arg343Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154966563C=CA2466848132F8c.1134G= (p.Arg378=)
c.*1010G= (n.*1010G=)
c.1029G= (p.Arg343=)
Xg.154966563C>GCA414916636F8c.1134G>C (p.Arg378Ser)
c.*1010G>C (n.*1010G>C)
c.1029G>C (p.Arg343Ser)
Xg.154966563C>TCA10568498F8c.1134G>A (p.Arg378=)
c.*1010G>A (n.*1010G>A)
c.1029G>A (p.Arg343=)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154966564delCA873344580F8c.1134del (p.Arg378SerfsTer?)
c.*1010del (n.*1010del)
c.1029del (p.Arg343SerfsTer?)
dbSNP
Xg.154966564C>ACA414916639F8c.1133G>T (p.Arg378Met)
c.*1009G>T (n.*1009G>T)
c.1028G>T (p.Arg343Met)
Xg.154966564C>GCA414916642F8c.1133G>C (p.Arg378Thr)
c.*1009G>C (n.*1009G>C)
c.1028G>C (p.Arg343Thr)
Xg.154966564C>TCA414916646F8c.1133G>A (p.Arg378Lys)
c.*1009G>A (n.*1009G>A)
c.1028G>A (p.Arg343Lys)
gnomAD v4
Xg.154966565T>ACA414916649F8c.1132A>T (p.Arg378Trp)
c.*1008A>T (n.*1008A>T)
c.1027A>T (p.Arg343Trp)
gnomAD v4
Xg.154966565T>CCA414916651F8c.1132A>G (p.Arg378Gly)
c.*1008A>G (n.*1008A>G)
c.1027A>G (p.Arg343Gly)
Xg.154966565T>GCA519365392F8c.1132A>C (p.Arg378=)
c.*1008A>C (n.*1008A>C)
c.1027A>C (p.Arg343=)
Xg.154966566G>ACA519365396F8c.1131C>T (p.Val377=)
c.*1007C>T (n.*1007C>T)
c.1026C>T (p.Val342=)
Xg.154966566G>CCA519365399F8c.1131C>G (p.Val377=)
c.*1007C>G (n.*1007C>G)
c.1026C>G (p.Val342=)
dbSNP
Xg.154966566G=CA2466848133F8c.1131C= (p.Val377=)
c.*1007C= (n.*1007C=)
c.1026C= (p.Val342=)
Xg.154966566G>TCA519365402F8c.1131C>A (p.Val377=)
c.*1007C>A (n.*1007C>A)
c.1026C>A (p.Val342=)
Xg.154966567A>CCA414916654F8c.1130T>G (p.Val377Gly)
c.*1006T>G (n.*1006T>G)
c.1025T>G (p.Val342Gly)
Xg.154966567A>GCA414916660F8c.1130T>C (p.Val377Ala)
c.*1006T>C (n.*1006T>C)
c.1025T>C (p.Val342Ala)
Xg.154966567A>TCA414916657F8c.1130T>A (p.Val377Asp)
c.*1006T>A (n.*1006T>A)
c.1025T>A (p.Val342Asp)
Xg.154966568C>ACA414916662F8c.1129G>T (p.Val377Phe)
c.*1005G>T (n.*1005G>T)
c.1024G>T (p.Val342Phe)
Xg.154966568C>GCA414916665F8c.1129G>C (p.Val377Leu)
c.*1005G>C (n.*1005G>C)
c.1024G>C (p.Val342Leu)

Number of alleles fetched