Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.141895341G>ACA10532718MAGEC3n.982G>A (p.Ala328Thr)
c.-118-1090G>A (p.=)
n.222G>A
c.-306G>A (p.=)
c.-229G>A (p.=)
dbSNP ExAC gnomAD
Xg.141895341G>CCA414436292MAGEC3n.982G>C (p.Ala328Pro)
c.-118-1090G>C (p.=)
n.222G>C
c.-306G>C (p.=)
c.-229G>C (p.=)
Xg.141895341G=CA2462229765MAGEC3n.982G= (p.Ala328=)
c.-118-1090G= (p.=)
n.222G=
c.-306G= (p.=)
c.-229G= (p.=)
Xg.141895341G>TCA414436294MAGEC3n.982G>T (p.Ala328Ser)
c.-118-1090G>T (p.=)
n.222G>T
c.-306G>T (p.=)
c.-229G>T (p.=)
Xg.141895342C>ACA414436297MAGEC3n.983C>A (p.Ala328Glu)
c.-118-1089C>A (p.=)
n.223C>A
c.-305C>A (p.=)
c.-228C>A (p.=)
Xg.141895342C>GCA414436303MAGEC3n.983C>G (p.Ala328Gly)
c.-118-1089C>G (p.=)
n.223C>G
c.-305C>G (p.=)
c.-228C>G (p.=)
Xg.141895342C>TCA414436318MAGEC3n.983C>T (p.Ala328Val)
c.-118-1089C>T (p.=)
n.223C>T
c.-305C>T (p.=)
c.-228C>T (p.=)
Xg.141895343A=CA2462229766MAGEC3n.984A= (p.Ala328=)
c.-118-1088A= (p.=)
n.224A=
c.-304A= (p.=)
c.-227A= (p.=)
Xg.141895343A>CCA518858287MAGEC3n.984A>C (p.Ala328=)
c.-118-1088A>C (p.=)
n.224A>C
c.-304A>C (p.=)
c.-227A>C (p.=)
Xg.141895343A>GCA518858291MAGEC3n.984A>G (p.Ala328=)
c.-118-1088A>G (p.=)
n.224A>G
c.-304A>G (p.=)
c.-227A>G (p.=)
gnomAD
Xg.141895343A>TCA518858292MAGEC3n.984A>T (p.Ala328=)
c.-118-1088A>T (p.=)
n.224A>T
c.-304A>T (p.=)
c.-227A>T (p.=)
Xg.141895344T>ACA414436341MAGEC3n.985T>A (p.Phe329Ile)
c.-118-1087T>A (p.=)
n.225T>A
c.-303T>A (p.=)
c.-226T>A (p.=)
Xg.141895344T>CCA414436358MAGEC3n.985T>C (p.Phe329Leu)
c.-118-1087T>C (p.=)
n.225T>C
c.-303T>C (p.=)
c.-226T>C (p.=)
Xg.141895344T>GCA414436346MAGEC3n.985T>G (p.Phe329Val)
c.-118-1087T>G (p.=)
n.225T>G
c.-303T>G (p.=)
c.-226T>G (p.=)
Xg.141895347dupCA872279458MAGEC3n.988dup (p.Cys330LeufsTer?)
c.-118-1084dup (p.=)
n.228dup
c.-300dup (p.=)
c.-223dup (p.=)
dbSNP
Xg.141895345T>ACA414436363MAGEC3n.986T>A (p.Phe329Tyr)
c.-118-1086T>A (p.=)
n.226T>A
c.-302T>A (p.=)
c.-225T>A (p.=)
Xg.141895345T>CCA414436367MAGEC3n.986T>C (p.Phe329Ser)
c.-118-1086T>C (p.=)
n.226T>C
c.-302T>C (p.=)
c.-225T>C (p.=)
Xg.141895345T>GCA414436368MAGEC3n.986T>G (p.Phe329Cys)
c.-118-1086T>G (p.=)
n.226T>G
c.-302T>G (p.=)
c.-225T>G (p.=)
Xg.141895345T=CA2462229767MAGEC3n.986T= (p.Phe329=)
c.-118-1086T= (p.=)
n.226T=
c.-302T= (p.=)
c.-225T= (p.=)
Xg.141895346T>ACA414436369MAGEC3n.987T>A (p.Phe329Leu)
c.-118-1085T>A (p.=)
n.227T>A
c.-301T>A (p.=)
c.-224T>A (p.=)
Xg.141895346T>CCA518858297MAGEC3n.987T>C (p.Phe329=)
c.-118-1085T>C (p.=)
n.227T>C
c.-301T>C (p.=)
c.-224T>C (p.=)
Xg.141895346T>GCA414436372MAGEC3n.987T>G (p.Phe329Leu)
c.-118-1085T>G (p.=)
n.227T>G
c.-301T>G (p.=)
c.-224T>G (p.=)
Xg.141895347T>ACA414436381MAGEC3n.988T>A (p.Cys330Ser)
c.-118-1084T>A (p.=)
n.228T>A
c.-300T>A (p.=)
c.-223T>A (p.=)
Xg.141895347T>CCA414436384MAGEC3n.988T>C (p.Cys330Arg)
c.-118-1084T>C (p.=)
n.228T>C
c.-300T>C (p.=)
c.-223T>C (p.=)
Xg.141895347T>GCA414436388MAGEC3n.988T>G (p.Cys330Gly)
c.-118-1084T>G (p.=)
n.228T>G
c.-300T>G (p.=)
c.-223T>G (p.=)
Xg.141895348G>ACA414436395MAGEC3n.989G>A (p.Cys330Tyr)
c.-118-1083G>A (p.=)
n.229G>A
c.-299G>A (p.=)
c.-222G>A (p.=)
Xg.141895348G>CCA414436398MAGEC3n.989G>C (p.Cys330Ser)
c.-118-1083G>C (p.=)
n.229G>C
c.-299G>C (p.=)
c.-222G>C (p.=)
Xg.141895348G>TCA414436401MAGEC3n.989G>T (p.Cys330Phe)
c.-118-1083G>T (p.=)
n.229G>T
c.-299G>T (p.=)
c.-222G>T (p.=)
Xg.141895349C>ACA414436417MAGEC3n.990C>A (p.Cys330Ter)
c.-118-1082C>A (p.=)
n.230C>A
c.-298C>A (p.=)
c.-221C>A (p.=)
Xg.141895349C=CA2462229768MAGEC3n.990C= (p.Cys330=)
c.-118-1082C= (p.=)
n.230C=
c.-298C= (p.=)
c.-221C= (p.=)
Xg.141895349C>GCA414436419MAGEC3n.990C>G (p.Cys330Trp)
c.-118-1082C>G (p.=)
n.230C>G
c.-298C>G (p.=)
c.-221C>G (p.=)
Xg.141895349C>TCA518858301MAGEC3n.990C>T (p.Cys330=)
c.-118-1082C>T (p.=)
n.230C>T
c.-298C>T (p.=)
c.-221C>T (p.=)
COSMIC
Xg.141895350G>ACA414436421MAGEC3n.991G>A (p.Glu331Lys)
c.-118-1081G>A (p.=)
n.231G>A
c.-297G>A (p.=)
c.-220G>A (p.=)
COSMIC COSMIC
Xg.141895350G>CCA414436424MAGEC3n.991G>C (p.Glu331Gln)
c.-118-1081G>C (p.=)
n.231G>C
c.-297G>C (p.=)
c.-220G>C (p.=)
COSMIC COSMIC
Xg.141895350G>TCA414436426MAGEC3n.991G>T (p.Glu331Ter)
c.-118-1081G>T (p.=)
n.231G>T
c.-297G>T (p.=)
c.-220G>T (p.=)
Xg.141895350_141895351delinsGACA2462229769MAGEC3n.991_992delinsGA (p.Glu331=)
c.-118-1081_-118-1080delinsGA (p.=)
n.231_232delinsGA
c.-297_-296delinsGA (p.=)
c.-220_-219delinsGA (p.=)
Xg.141895351delCA1137911403MAGEC3n.992del (p.Glu331GlyfsTer13)
c.-118-1080del (p.=)
n.232del
c.-296del (p.=)
c.-219del (p.=)
dbSNP
Xg.141895351A=CA2462229770MAGEC3n.992A= (p.Glu331=)
c.-118-1080A= (p.=)
n.232A=
c.-296A= (p.=)
c.-219A= (p.=)
Xg.141895351A>CCA414436428MAGEC3n.992A>C (p.Glu331Ala)
c.-118-1080A>C (p.=)
n.232A>C
c.-296A>C (p.=)
c.-219A>C (p.=)
Xg.141895351A>GCA414436449MAGEC3n.992A>G (p.Glu331Gly)
c.-118-1080A>G (p.=)
n.232A>G
c.-296A>G (p.=)
c.-219A>G (p.=)
Xg.141895351A>TCA414436456MAGEC3n.992A>T (p.Glu331Val)
c.-118-1080A>T (p.=)
n.232A>T
c.-296A>T (p.=)
c.-219A>T (p.=)
Xg.141895352G>ACA518858304MAGEC3n.993G>A (p.Glu331=)
c.-118-1079G>A (p.=)
n.233G>A
c.-295G>A (p.=)
c.-218G>A (p.=)
COSMIC COSMIC
Xg.141895352G>CCA414436462MAGEC3n.993G>C (p.Glu331Asp)
c.-118-1079G>C (p.=)
n.233G>C
c.-295G>C (p.=)
c.-218G>C (p.=)
Xg.141895352G>TCA414436465MAGEC3n.993G>T (p.Glu331Asp)
c.-118-1079G>T (p.=)
n.233G>T
c.-295G>T (p.=)
c.-218G>T (p.=)
Xg.141895353G>ACA414436472MAGEC3n.994G>A (p.Glu332Lys)
c.-118-1078G>A (p.=)
n.234G>A
c.-294G>A (p.=)
c.-217G>A (p.=)
COSMIC
Xg.141895353G>CCA414436475MAGEC3n.994G>C (p.Glu332Gln)
c.-118-1078G>C (p.=)
n.234G>C
c.-294G>C (p.=)
c.-217G>C (p.=)
COSMIC COSMIC
Xg.141895353G>TCA414436477MAGEC3n.994G>T (p.Glu332Ter)
c.-118-1078G>T (p.=)
n.234G>T
c.-294G>T (p.=)
c.-217G>T (p.=)
Xg.141895354A>CCA414436478MAGEC3n.995A>C (p.Glu332Ala)
c.-118-1077A>C (p.=)
n.235A>C
c.-293A>C (p.=)
c.-216A>C (p.=)
Xg.141895354A>GCA414436479MAGEC3n.995A>G (p.Glu332Gly)
c.-118-1077A>G (p.=)
n.235A>G
c.-293A>G (p.=)
c.-216A>G (p.=)
Xg.141895354A>TCA414436480MAGEC3n.995A>T (p.Glu332Val)
c.-118-1077A>T (p.=)
n.235A>T
c.-293A>T (p.=)
c.-216A>T (p.=)

Number of alleles fetched