Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.51138827T>ACA395880357SALL1c.3395A>T (p.Lys1132Met)
c.3104A>T (p.Lys1035Met)
c.77-1275A>T (n.77-1275A>T)
 dbSNP
16g.51138827T>CCA8052935SALL1c.3395A>G (p.Lys1132Arg)
c.3104A>G (p.Lys1035Arg)
c.77-1275A>G (n.77-1275A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.51138827T>GCA395880355SALL1c.3395A>C (p.Lys1132Thr)
c.3104A>C (p.Lys1035Thr)
c.77-1275A>C (n.77-1275A>C)
16g.51138827T=CA2222016832SALL1c.3395A= (p.Lys1132=)
c.3104A= (p.Lys1035=)
c.77-1275A= (n.77-1275A=)
16g.51138828T>ACA395880359SALL1c.3394A>T (p.Lys1132Ter)
c.3103A>T (p.Lys1035Ter)
c.77-1276A>T (n.77-1276A>T)
16g.51138828T>CCA395880361SALL1c.3394A>G (p.Lys1132Glu)
c.3103A>G (p.Lys1035Glu)
c.77-1276A>G (n.77-1276A>G)
16g.51138828T>GCA395880363SALL1c.3394A>C (p.Lys1132Gln)
c.3103A>C (p.Lys1035Gln)
c.77-1276A>C (n.77-1276A>C)
16g.51138829G>ACA495779753SALL1c.3393C>T (p.Pro1131=)
c.3102C>T (p.Pro1034=)
c.77-1277C>T (n.77-1277C>T)
16g.51138829G>CCA495779754SALL1c.3393C>G (p.Pro1131=)
c.3102C>G (p.Pro1034=)
c.77-1277C>G (n.77-1277C>G)
16g.51138829G=CA2222016837SALL1c.3393C= (p.Pro1131=)
c.3102C= (p.Pro1034=)
c.77-1277C= (n.77-1277C=)
16g.51138829G>TCA8052936SALL1c.3393C>A (p.Pro1131=)
c.3102C>A (p.Pro1034=)
c.77-1277C>A (n.77-1277C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51138830G>ACA395880367SALL1c.3392C>T (p.Pro1131Leu)
c.3101C>T (p.Pro1034Leu)
c.77-1278C>T (n.77-1278C>T)
16g.51138830G>CCA395880369SALL1c.3392C>G (p.Pro1131Arg)
c.3101C>G (p.Pro1034Arg)
c.77-1278C>G (n.77-1278C>G)
16g.51138830G>TCA395880370SALL1c.3392C>A (p.Pro1131His)
c.3101C>A (p.Pro1034His)
c.77-1278C>A (n.77-1278C>A)
16g.51138831G>ACA395880373SALL1c.3391C>T (p.Pro1131Ser)
c.3100C>T (p.Pro1034Ser)
c.77-1279C>T (n.77-1279C>T)
16g.51138831G>CCA395880375SALL1c.3391C>G (p.Pro1131Ala)
c.3100C>G (p.Pro1034Ala)
c.77-1279C>G (n.77-1279C>G)
16g.51138831G>TCA395880377SALL1c.3391C>A (p.Pro1131Thr)
c.3100C>A (p.Pro1034Thr)
c.77-1279C>A (n.77-1279C>A)
16g.51138832A=CA2222016839SALL1c.3390T= (p.Thr1130=)
c.3099T= (p.Thr1033=)
c.77-1280T= (n.77-1280T=)
16g.51138832A>CCA495779756SALL1c.3390T>G (p.Thr1130=)
c.3099T>G (p.Thr1033=)
c.77-1280T>G (n.77-1280T>G)
16g.51138832A>GCA281300585SALL1c.3390T>C (p.Thr1130=)
c.3099T>C (p.Thr1033=)
c.77-1280T>C (n.77-1280T>C)
 dbSNP
16g.51138832A>TCA495779757SALL1c.3390T>A (p.Thr1130=)
c.3099T>A (p.Thr1033=)
c.77-1280T>A (n.77-1280T>A)
 gnomAD v4
16g.51138833G>ACA395880379SALL1c.3389C>T (p.Thr1130Ile)
c.3098C>T (p.Thr1033Ile)
c.77-1281C>T (n.77-1281C>T)
16g.51138833G>CCA395880381SALL1c.3389C>G (p.Thr1130Ser)
c.3098C>G (p.Thr1033Ser)
c.77-1281C>G (n.77-1281C>G)
16g.51138833G>TCA395880384SALL1c.3389C>A (p.Thr1130Asn)
c.3098C>A (p.Thr1033Asn)
c.77-1281C>A (n.77-1281C>A)
16g.51138834T>ACA395880390SALL1c.3388A>T (p.Thr1130Ser)
c.3097A>T (p.Thr1033Ser)
c.77-1282A>T (n.77-1282A>T)
16g.51138834T>CCA395880388SALL1c.3388A>G (p.Thr1130Ala)
c.3097A>G (p.Thr1033Ala)
c.77-1282A>G (n.77-1282A>G)
 dbSNP gnomAD v4
16g.51138834T>GCA395880386SALL1c.3388A>C (p.Thr1130Pro)
c.3097A>C (p.Thr1033Pro)
c.77-1282A>C (n.77-1282A>C)
16g.51138834T=CA2222016853SALL1c.3388A= (p.Thr1130=)
c.3097A= (p.Thr1033=)
c.77-1282A= (n.77-1282A=)
16g.51138835T>ACA395880392SALL1c.3387A>T (p.Arg1129Ser)
c.3096A>T (p.Arg1032Ser)
c.77-1283A>T (n.77-1283A>T)
 dbSNP gnomAD v2 gnomAD v4
16g.51138835T>CCA495779758SALL1c.3387A>G (p.Arg1129=)
c.3096A>G (p.Arg1032=)
c.77-1283A>G (n.77-1283A>G)
16g.51138835T>GCA395880394SALL1c.3387A>C (p.Arg1129Ser)
c.3096A>C (p.Arg1032Ser)
c.77-1283A>C (n.77-1283A>C)
16g.51138835T=CA2222016856SALL1c.3387A= (p.Arg1129=)
c.3096A= (p.Arg1032=)
c.77-1283A= (n.77-1283A=)
16g.51138836C>ACA395880396SALL1c.3386G>T (p.Arg1129Ile)
c.3095G>T (p.Arg1032Ile)
c.77-1284G>T (n.77-1284G>T)
16g.51138836C>GCA395880399SALL1c.3386G>C (p.Arg1129Thr)
c.3095G>C (p.Arg1032Thr)
c.77-1284G>C (n.77-1284G>C)
16g.51138836C>TCA395880401SALL1c.3386G>A (p.Arg1129Lys)
c.3095G>A (p.Arg1032Lys)
c.77-1284G>A (n.77-1284G>A)
16g.51138837T>ACA395880403SALL1c.3385A>T (p.Arg1129Ter)
c.3094A>T (p.Arg1032Ter)
c.77-1285A>T (n.77-1285A>T)
16g.51138837T>CCA395880405SALL1c.3385A>G (p.Arg1129Gly)
c.3094A>G (p.Arg1032Gly)
c.77-1285A>G (n.77-1285A>G)
16g.51138837T>GCA495779760SALL1c.3385A>C (p.Arg1129=)
c.3094A>C (p.Arg1032=)
c.77-1285A>C (n.77-1285A>C)
16g.51138838C>ACA395880407SALL1c.3384G>T (p.Arg1128Ser)
c.3093G>T (p.Arg1031Ser)
c.77-1286G>T (n.77-1286G>T)
16g.51138838C=CA2222016860SALL1c.3384G= (p.Arg1128=)
c.3093G= (p.Arg1031=)
c.77-1286G= (n.77-1286G=)
16g.51138838C>GCA395880409SALL1c.3384G>C (p.Arg1128Ser)
c.3093G>C (p.Arg1031Ser)
c.77-1286G>C (n.77-1286G>C)
16g.51138838C>TCA495779761SALL1c.3384G>A (p.Arg1128=)
c.3093G>A (p.Arg1031=)
c.77-1286G>A (n.77-1286G>A)
 dbSNP gnomAD v2 gnomAD v4
16g.51138839C>ACA395880411SALL1c.3383G>T (p.Arg1128Met)
c.3092G>T (p.Arg1031Met)
c.77-1287G>T (n.77-1287G>T)
16g.51138839C=CA2222016864SALL1c.3383G= (p.Arg1128=)
c.3092G= (p.Arg1031=)
c.77-1287G= (n.77-1287G=)
16g.51138839C>GCA395880413SALL1c.3383G>C (p.Arg1128Thr)
c.3092G>C (p.Arg1031Thr)
c.77-1287G>C (n.77-1287G>C)
 dbSNP gnomAD v3 gnomAD v4
16g.51138839C>TCA395880414SALL1c.3383G>A (p.Arg1128Lys)
c.3092G>A (p.Arg1031Lys)
c.77-1287G>A (n.77-1287G>A)
16g.51138840T>ACA395880416SALL1c.3382A>T (p.Arg1128Trp)
c.3091A>T (p.Arg1031Trp)
c.77-1288A>T (n.77-1288A>T)
 gnomAD v4
16g.51138840T>CCA395880418SALL1c.3382A>G (p.Arg1128Gly)
c.3091A>G (p.Arg1031Gly)
c.77-1288A>G (n.77-1288A>G)
16g.51138840T>GCA495779763SALL1c.3382A>C (p.Arg1128=)
c.3091A>C (p.Arg1031=)
c.77-1288A>C (n.77-1288A>C)
16g.51138841G>ACA495779764SALL1c.3381C>T (p.Pro1127=)
c.3090C>T (p.Pro1030=)
c.77-1289C>T (n.77-1289C>T)
16g.51138841G>CCA495779765SALL1c.3381C>G (p.Pro1127=)
c.3090C>G (p.Pro1030=)
c.77-1289C>G (n.77-1289C>G)
16g.51138841G>TCA495779766SALL1c.3381C>A (p.Pro1127=)
c.3090C>A (p.Pro1030=)
c.77-1289C>A (n.77-1289C>A)
16g.51138843delCA2573054235SALL1c.3381del (p.Arg1128GlyfsTer?)
c.3090del (p.Arg1031GlyfsTer?)
c.77-1289del (n.77-1289del)
 ClinVar dbSNP
16g.51138842G>ACA8052937SALL1c.3380C>T (p.Pro1127Leu)
c.3089C>T (p.Pro1030Leu)
c.77-1290C>T (n.77-1290C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.51138842G>CCA395880422SALL1c.3380C>G (p.Pro1127Arg)
c.3089C>G (p.Pro1030Arg)
c.77-1290C>G (n.77-1290C>G)
16g.51138842G=CA2222016869SALL1c.3380C= (p.Pro1127=)
c.3089C= (p.Pro1030=)
c.77-1290C= (n.77-1290C=)
16g.51138842G>TCA395880420SALL1c.3380C>A (p.Pro1127His)
c.3089C>A (p.Pro1030His)
c.77-1290C>A (n.77-1290C>A)
16g.51138843G>ACA395880424SALL1c.3379C>T (p.Pro1127Ser)
c.3088C>T (p.Pro1030Ser)
c.77-1291C>T (n.77-1291C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.51138843G>CCA395880426SALL1c.3379C>G (p.Pro1127Ala)
c.3088C>G (p.Pro1030Ala)
c.77-1291C>G (n.77-1291C>G)
16g.51138843G=CA2222016870SALL1c.3379C= (p.Pro1127=)
c.3088C= (p.Pro1030=)
c.77-1291C= (n.77-1291C=)
16g.51138843G>TCA395880428SALL1c.3379C>A (p.Pro1127Thr)
c.3088C>A (p.Pro1030Thr)
c.77-1291C>A (n.77-1291C>A)
16g.51138844C>ACA495779767SALL1c.3378G>T (p.Leu1126=)
c.3087G>T (p.Leu1029=)
c.77-1292G>T (n.77-1292G>T)
 gnomAD v4
16g.51138844C>GCA495779769SALL1c.3378G>C (p.Leu1126=)
c.3087G>C (p.Leu1029=)
c.77-1292G>C (n.77-1292G>C)
16g.51138844C>TCA495779768SALL1c.3378G>A (p.Leu1126=)
c.3087G>A (p.Leu1029=)
c.77-1292G>A (n.77-1292G>A)
16g.51138845A=CA2222016872SALL1c.3377T= (p.Leu1126=)
c.3086T= (p.Leu1029=)
c.77-1293T= (n.77-1293T=)
16g.51138845A>CCA395880430SALL1c.3377T>G (p.Leu1126Arg)
c.3086T>G (p.Leu1029Arg)
c.77-1293T>G (n.77-1293T>G)
16g.51138845A>GCA395880432SALL1c.3377T>C (p.Leu1126Pro)
c.3086T>C (p.Leu1029Pro)
c.77-1293T>C (n.77-1293T>C)
16g.51138845A>TCA8052938SALL1c.3377T>A (p.Leu1126Gln)
c.3086T>A (p.Leu1029Gln)
c.77-1293T>A (n.77-1293T>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138846G>ACA495779773SALL1c.3376C>T (p.Leu1126=)
c.3085C>T (p.Leu1029=)
c.77-1294C>T (n.77-1294C>T)
 dbSNP
16g.51138846G>CCA395880435SALL1c.3376C>G (p.Leu1126Val)
c.3085C>G (p.Leu1029Val)
c.77-1294C>G (n.77-1294C>G)
16g.51138846G=CA2222016876SALL1c.3376C= (p.Leu1126=)
c.3085C= (p.Leu1029=)
c.77-1294C= (n.77-1294C=)
16g.51138846G>TCA395880438SALL1c.3376C>A (p.Leu1126Met)
c.3085C>A (p.Leu1029Met)
c.77-1294C>A (n.77-1294C>A)
16g.51138847A>CCA495779774SALL1c.3375T>G (p.Ala1125=)
c.3084T>G (p.Ala1028=)
c.77-1295T>G (n.77-1295T>G)
16g.51138847A>GCA495779775SALL1c.3375T>C (p.Ala1125=)
c.3084T>C (p.Ala1028=)
c.77-1295T>C (n.77-1295T>C)
16g.51138847A>TCA495779776SALL1c.3375T>A (p.Ala1125=)
c.3084T>A (p.Ala1028=)
c.77-1295T>A (n.77-1295T>A)
16g.51138848G>ACA395880440SALL1c.3374C>T (p.Ala1125Val)
c.3083C>T (p.Ala1028Val)
c.77-1296C>T (n.77-1296C>T)
 dbSNP
16g.51138848G>CCA395880442SALL1c.3374C>G (p.Ala1125Gly)
c.3083C>G (p.Ala1028Gly)
c.77-1296C>G (n.77-1296C>G)
16g.51138848G=CA2222016879SALL1c.3374C= (p.Ala1125=)
c.3083C= (p.Ala1028=)
c.77-1296C= (n.77-1296C=)
16g.51138848G>TCA395880443SALL1c.3374C>A (p.Ala1125Asp)
c.3083C>A (p.Ala1028Asp)
c.77-1296C>A (n.77-1296C>A)
16g.51138849C>ACA8052939SALL1c.3373G>T (p.Ala1125Ser)
c.3082G>T (p.Ala1028Ser)
c.77-1297G>T (n.77-1297G>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138849C=CA2222016883SALL1c.3373G= (p.Ala1125=)
c.3082G= (p.Ala1028=)
c.77-1297G= (n.77-1297G=)
16g.51138849C>GCA395880449SALL1c.3373G>C (p.Ala1125Pro)
c.3082G>C (p.Ala1028Pro)
c.77-1297G>C (n.77-1297G>C)
16g.51138849C>TCA395880447SALL1c.3373G>A (p.Ala1125Thr)
c.3082G>A (p.Ala1028Thr)
c.77-1297G>A (n.77-1297G>A)
16g.51138850A=CA2222016888SALL1c.3372T= (p.Pro1124=)
c.3081T= (p.Pro1027=)
c.77-1298T= (n.77-1298T=)
16g.51138850A>CCA495779780SALL1c.3372T>G (p.Pro1124=)
c.3081T>G (p.Pro1027=)
c.77-1298T>G (n.77-1298T>G)
16g.51138850A>GCA495779781SALL1c.3372T>C (p.Pro1124=)
c.3081T>C (p.Pro1027=)
c.77-1298T>C (n.77-1298T>C)
16g.51138850A>TCA495779782SALL1c.3372T>A (p.Pro1124=)
c.3081T>A (p.Pro1027=)
c.77-1298T>A (n.77-1298T>A)
 dbSNP
16g.51138851G>ACA395880452SALL1c.3371C>T (p.Pro1124Leu)
c.3080C>T (p.Pro1027Leu)
c.77-1299C>T (n.77-1299C>T)
16g.51138851G>CCA395880457SALL1c.3371C>G (p.Pro1124Arg)
c.3080C>G (p.Pro1027Arg)
c.77-1299C>G (n.77-1299C>G)
 dbSNP
16g.51138851G>TCA395880454SALL1c.3371C>A (p.Pro1124His)
c.3080C>A (p.Pro1027His)
c.77-1299C>A (n.77-1299C>A)
16g.51138852G>ACA395880459SALL1c.3370C>T (p.Pro1124Ser)
c.3079C>T (p.Pro1027Ser)
c.77-1300C>T (n.77-1300C>T)
16g.51138852G>CCA395880461SALL1c.3370C>G (p.Pro1124Ala)
c.3079C>G (p.Pro1027Ala)
c.77-1300C>G (n.77-1300C>G)
16g.51138852G>TCA395880463SALL1c.3370C>A (p.Pro1124Thr)
c.3079C>A (p.Pro1027Thr)
c.77-1300C>A (n.77-1300C>A)
16g.51138853G>ACA8052940SALL1c.3369C>T (p.Leu1123=)
c.3078C>T (p.Leu1026=)
c.77-1301C>T (n.77-1301C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.51138853G>CCA495779783SALL1c.3369C>G (p.Leu1123=)
c.3078C>G (p.Leu1026=)
c.77-1301C>G (n.77-1301C>G)
 gnomAD v4
16g.51138853G=CA2222016891SALL1c.3369C= (p.Leu1123=)
c.3078C= (p.Leu1026=)
c.77-1301C= (n.77-1301C=)
16g.51138853G>TCA495779784SALL1c.3369C>A (p.Leu1123=)
c.3078C>A (p.Leu1026=)
c.77-1301C>A (n.77-1301C>A)
16g.51138854A>CCA395880465SALL1c.3368T>G (p.Leu1123Arg)
c.3077T>G (p.Leu1026Arg)
c.77-1302T>G (n.77-1302T>G)
16g.51138854A>GCA395880467SALL1c.3368T>C (p.Leu1123Pro)
c.3077T>C (p.Leu1026Pro)
c.77-1302T>C (n.77-1302T>C)
16g.51138854A>TCA395880468SALL1c.3368T>A (p.Leu1123His)
c.3077T>A (p.Leu1026His)
c.77-1302T>A (n.77-1302T>A)
16g.51138855G>ACA395880470SALL1c.3367C>T (p.Leu1123Phe)
c.3076C>T (p.Leu1026Phe)
c.77-1303C>T (n.77-1303C>T)
16g.51138855G>CCA395880472SALL1c.3367C>G (p.Leu1123Val)
c.3076C>G (p.Leu1026Val)
c.77-1303C>G (n.77-1303C>G)
 gnomAD v4
16g.51138855G>TCA395880473SALL1c.3367C>A (p.Leu1123Ile)
c.3076C>A (p.Leu1026Ile)
c.77-1303C>A (n.77-1303C>A)
16g.51138856C>ACA495779788SALL1c.3366G>T (p.Leu1122=)
c.3075G>T (p.Leu1025=)
c.77-1304G>T (n.77-1304G>T)
 gnomAD v4
16g.51138856C>GCA495779789SALL1c.3366G>C (p.Leu1122=)
c.3075G>C (p.Leu1025=)
c.77-1304G>C (n.77-1304G>C)
16g.51138856C>TCA495779790SALL1c.3366G>A (p.Leu1122=)
c.3075G>A (p.Leu1025=)
c.77-1304G>A (n.77-1304G>A)
16g.51138857A=CA2222016895SALL1c.3365T= (p.Leu1122=)
c.3074T= (p.Leu1025=)
c.77-1305T= (n.77-1305T=)
16g.51138857A>CCA395880480SALL1c.3365T>G (p.Leu1122Arg)
c.3074T>G (p.Leu1025Arg)
c.77-1305T>G (n.77-1305T>G)
16g.51138857A>GCA8052941SALL1c.3365T>C (p.Leu1122Pro)
c.3074T>C (p.Leu1025Pro)
c.77-1305T>C (n.77-1305T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
16g.51138857A>TCA395880476SALL1c.3365T>A (p.Leu1122Gln)
c.3074T>A (p.Leu1025Gln)
c.77-1305T>A (n.77-1305T>A)
16g.51138858G>ACA495779791SALL1c.3364C>T (p.Leu1122=)
c.3073C>T (p.Leu1025=)
c.77-1306C>T (n.77-1306C>T)
16g.51138858G>CCA395880481SALL1c.3364C>G (p.Leu1122Val)
c.3073C>G (p.Leu1025Val)
c.77-1306C>G (n.77-1306C>G)
 gnomAD v4
16g.51138858G>TCA395880482SALL1c.3364C>A (p.Leu1122Met)
c.3073C>A (p.Leu1025Met)
c.77-1306C>A (n.77-1306C>A)
16g.51138859A=CA2222016901SALL1c.3363T= (p.Val1121=)
c.3072T= (p.Val1024=)
c.77-1307T= (n.77-1307T=)
16g.51138859A>CCA495779793SALL1c.3363T>G (p.Val1121=)
c.3072T>G (p.Val1024=)
c.77-1307T>G (n.77-1307T>G)
16g.51138859A>GCA495779794SALL1c.3363T>C (p.Val1121=)
c.3072T>C (p.Val1024=)
c.77-1307T>C (n.77-1307T>C)
 dbSNP
16g.51138859A>TCA495779796SALL1c.3363T>A (p.Val1121=)
c.3072T>A (p.Val1024=)
c.77-1307T>A (n.77-1307T>A)
16g.51138860A=CA2222016904SALL1c.3362T= (p.Val1121=)
c.3071T= (p.Val1024=)
c.77-1308T= (n.77-1308T=)
16g.51138860A>CCA395880486SALL1c.3362T>G (p.Val1121Gly)
c.3071T>G (p.Val1024Gly)
c.77-1308T>G (n.77-1308T>G)
16g.51138860A>GCA8052942SALL1c.3362T>C (p.Val1121Ala)
c.3071T>C (p.Val1024Ala)
c.77-1308T>C (n.77-1308T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51138860A>TCA395880489SALL1c.3362T>A (p.Val1121Asp)
c.3071T>A (p.Val1024Asp)
c.77-1308T>A (n.77-1308T>A)
16g.51138861C>ACA395880491SALL1c.3361G>T (p.Val1121Phe)
c.3070G>T (p.Val1024Phe)
c.77-1309G>T (n.77-1309G>T)
 gnomAD v4
16g.51138861C>GCA395880492SALL1c.3361G>C (p.Val1121Leu)
c.3070G>C (p.Val1024Leu)
c.77-1309G>C (n.77-1309G>C)
16g.51138861C>TCA395880495SALL1c.3361G>A (p.Val1121Ile)
c.3070G>A (p.Val1024Ile)
c.77-1309G>A (n.77-1309G>A)
16g.51138862T>ACA495779798SALL1c.3360A>T (p.Pro1120=)
c.3069A>T (p.Pro1023=)
c.77-1310A>T (n.77-1310A>T)
16g.51138862T>CCA495779799SALL1c.3360A>G (p.Pro1120=)
c.3069A>G (p.Pro1023=)
c.77-1310A>G (n.77-1310A>G)
 gnomAD v4
16g.51138862T>GCA495779800SALL1c.3360A>C (p.Pro1120=)
c.3069A>C (p.Pro1023=)
c.77-1310A>C (n.77-1310A>C)
16g.51138863G>ACA395880497SALL1c.3359C>T (p.Pro1120Leu)
c.3068C>T (p.Pro1023Leu)
c.77-1311C>T (n.77-1311C>T)
 gnomAD v4
16g.51138863G>CCA395880499SALL1c.3359C>G (p.Pro1120Arg)
c.3068C>G (p.Pro1023Arg)
c.77-1311C>G (n.77-1311C>G)
16g.51138863G>TCA395880501SALL1c.3359C>A (p.Pro1120Gln)
c.3068C>A (p.Pro1023Gln)
c.77-1311C>A (n.77-1311C>A)
16g.51138864G>ACA395880505SALL1c.3358C>T (p.Pro1120Ser)
c.3067C>T (p.Pro1023Ser)
c.77-1312C>T (n.77-1312C>T)
16g.51138864G>CCA395880507SALL1c.3358C>G (p.Pro1120Ala)
c.3067C>G (p.Pro1023Ala)
c.77-1312C>G (n.77-1312C>G)
16g.51138864G>TCA395880503SALL1c.3358C>A (p.Pro1120Thr)
c.3067C>A (p.Pro1023Thr)
c.77-1312C>A (n.77-1312C>A)
16g.51138865G>ACA495779803SALL1c.3357C>T (p.Ser1119=)
c.3066C>T (p.Ser1022=)
c.77-1313C>T (n.77-1313C>T)
 dbSNP gnomAD v2 gnomAD v4
16g.51138865G>CCA495779805SALL1c.3357C>G (p.Ser1119=)
c.3066C>G (p.Ser1022=)
c.77-1313C>G (n.77-1313C>G)
16g.51138865G=CA2222016906SALL1c.3357C= (p.Ser1119=)
c.3066C= (p.Ser1022=)
c.77-1313C= (n.77-1313C=)
16g.51138865G>TCA495779806SALL1c.3357C>A (p.Ser1119=)
c.3066C>A (p.Ser1022=)
c.77-1313C>A (n.77-1313C>A)
16g.51138866G>ACA281300599SALL1c.3356C>T (p.Ser1119Phe)
c.3065C>T (p.Ser1022Phe)
c.77-1314C>T (n.77-1314C>T)
 dbSNP
16g.51138866G>CCA395880513SALL1c.3356C>G (p.Ser1119Cys)
c.3065C>G (p.Ser1022Cys)
c.77-1314C>G (n.77-1314C>G)
16g.51138866G=CA2222016910SALL1c.3356C= (p.Ser1119=)
c.3065C= (p.Ser1022=)
c.77-1314C= (n.77-1314C=)
16g.51138866G>TCA395880516SALL1c.3356C>A (p.Ser1119Tyr)
c.3065C>A (p.Ser1022Tyr)
c.77-1314C>A (n.77-1314C>A)
 gnomAD v4
16g.51138867A=CA2222016913SALL1c.3355T= (p.Ser1119=)
c.3064T= (p.Ser1022=)
c.77-1315T= (n.77-1315T=)
16g.51138867A>CCA395880518SALL1c.3355T>G (p.Ser1119Ala)
c.3064T>G (p.Ser1022Ala)
c.77-1315T>G (n.77-1315T>G)
 gnomAD v4
16g.51138867A>GCA8052943SALL1c.3355T>C (p.Ser1119Pro)
c.3064T>C (p.Ser1022Pro)
c.77-1315T>C (n.77-1315T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51138867A>TCA395880520SALL1c.3355T>A (p.Ser1119Thr)
c.3064T>A (p.Ser1022Thr)
c.77-1315T>A (n.77-1315T>A)
16g.51138868T>ACA495779807SALL1c.3354A>T (p.Thr1118=)
c.3063A>T (p.Thr1021=)
c.77-1316A>T (n.77-1316A>T)
 gnomAD v4
16g.51138868T>CCA495779808SALL1c.3354A>G (p.Thr1118=)
c.3063A>G (p.Thr1021=)
c.77-1316A>G (n.77-1316A>G)
 gnomAD v4
16g.51138868T>GCA495779809SALL1c.3354A>C (p.Thr1118=)
c.3063A>C (p.Thr1021=)
c.77-1316A>C (n.77-1316A>C)
16g.51138869G>ACA395880537SALL1c.3353C>T (p.Thr1118Ile)
c.3062C>T (p.Thr1021Ile)
c.77-1317C>T (n.77-1317C>T)
16g.51138869G>CCA395880540SALL1c.3353C>G (p.Thr1118Arg)
c.3062C>G (p.Thr1021Arg)
c.77-1317C>G (n.77-1317C>G)
16g.51138869G>TCA395880543SALL1c.3353C>A (p.Thr1118Lys)
c.3062C>A (p.Thr1021Lys)
c.77-1317C>A (n.77-1317C>A)
16g.51138870T>ACA395880546SALL1c.3352A>T (p.Thr1118Ser)
c.3061A>T (p.Thr1021Ser)
c.77-1318A>T (n.77-1318A>T)
16g.51138870T>CCA395880559SALL1c.3352A>G (p.Thr1118Ala)
c.3061A>G (p.Thr1021Ala)
c.77-1318A>G (n.77-1318A>G)
 dbSNP
16g.51138870T>GCA395880563SALL1c.3352A>C (p.Thr1118Pro)
c.3061A>C (p.Thr1021Pro)
c.77-1318A>C (n.77-1318A>C)
16g.51138870T=CA2222016918SALL1c.3352A= (p.Thr1118=)
c.3061A= (p.Thr1021=)
c.77-1318A= (n.77-1318A=)
16g.51138871G>ACA495779813SALL1c.3351C>T (p.Ala1117=)
c.3060C>T (p.Ala1020=)
c.77-1319C>T (n.77-1319C>T)
 dbSNP
16g.51138871G>CCA495779812SALL1c.3351C>G (p.Ala1117=)
c.3060C>G (p.Ala1020=)
c.77-1319C>G (n.77-1319C>G)
16g.51138871G=CA2222016925SALL1c.3351C= (p.Ala1117=)
c.3060C= (p.Ala1020=)
c.77-1319C= (n.77-1319C=)
16g.51138871G>TCA495779811SALL1c.3351C>A (p.Ala1117=)
c.3060C>A (p.Ala1020=)
c.77-1319C>A (n.77-1319C>A)
16g.51138871_51138873dupCA2553379064SALL1c.3349_3351dup (p.Ala1117_Thr1118insAla)
c.3058_3060dup (p.Ala1020_Thr1021insAla)
c.77-1321_77-1319dup (n.77-1321_77-1319dup)
16g.51138872G>ACA395880570SALL1c.3350C>T (p.Ala1117Val)
c.3059C>T (p.Ala1020Val)
c.77-1320C>T (n.77-1320C>T)
16g.51138872G>CCA395880566SALL1c.3350C>G (p.Ala1117Gly)
c.3059C>G (p.Ala1020Gly)
c.77-1320C>G (n.77-1320C>G)
16g.51138872G>TCA395880568SALL1c.3350C>A (p.Ala1117Asp)
c.3059C>A (p.Ala1020Asp)
c.77-1320C>A (n.77-1320C>A)
16g.51138873C>ACA395880573SALL1c.3349G>T (p.Ala1117Ser)
c.3058G>T (p.Ala1020Ser)
c.77-1321G>T (n.77-1321G>T)
16g.51138873C=CA2222016927SALL1c.3349G= (p.Ala1117=)
c.3058G= (p.Ala1020=)
c.77-1321G= (n.77-1321G=)
16g.51138873C>GCA395880576SALL1c.3349G>C (p.Ala1117Pro)
c.3058G>C (p.Ala1020Pro)
c.77-1321G>C (n.77-1321G>C)
16g.51138873C>TCA395880580SALL1c.3349G>A (p.Ala1117Thr)
c.3058G>A (p.Ala1020Thr)
c.77-1321G>A (n.77-1321G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.51138874A>CCA495779815SALL1c.3348T>G (p.Ser1116=)
c.3057T>G (p.Ser1019=)
c.77-1322T>G (n.77-1322T>G)
16g.51138874A>GCA495779816SALL1c.3348T>C (p.Ser1116=)
c.3057T>C (p.Ser1019=)
c.77-1322T>C (n.77-1322T>C)
16g.51138874A>TCA495779817SALL1c.3348T>A (p.Ser1116=)
c.3057T>A (p.Ser1019=)
c.77-1322T>A (n.77-1322T>A)
16g.51138875G>ACA8052944SALL1c.3347C>T (p.Ser1116Phe)
c.3056C>T (p.Ser1019Phe)
c.77-1323C>T (n.77-1323C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138875G>CCA395880583SALL1c.3347C>G (p.Ser1116Cys)
c.3056C>G (p.Ser1019Cys)
c.77-1323C>G (n.77-1323C>G)
16g.51138875G=CA2222016931SALL1c.3347C= (p.Ser1116=)
c.3056C= (p.Ser1019=)
c.77-1323C= (n.77-1323C=)
16g.51138875G>TCA395880585SALL1c.3347C>A (p.Ser1116Tyr)
c.3056C>A (p.Ser1019Tyr)
c.77-1323C>A (n.77-1323C>A)
16g.51138876A>CCA395880588SALL1c.3346T>G (p.Ser1116Ala)
c.3055T>G (p.Ser1019Ala)
c.77-1324T>G (n.77-1324T>G)
16g.51138876A>GCA395880590SALL1c.3346T>C (p.Ser1116Pro)
c.3055T>C (p.Ser1019Pro)
c.77-1324T>C (n.77-1324T>C)
16g.51138876A>TCA395880593SALL1c.3346T>A (p.Ser1116Thr)
c.3055T>A (p.Ser1019Thr)
c.77-1324T>A (n.77-1324T>A)
16g.51138877G>ACA495779819SALL1c.3345C>T (p.Ser1115=)
c.3054C>T (p.Ser1018=)
c.77-1325C>T (n.77-1325C>T)
16g.51138877G>CCA495779821SALL1c.3345C>G (p.Ser1115=)
c.3054C>G (p.Ser1018=)
c.77-1325C>G (n.77-1325C>G)
 gnomAD v4
16g.51138877G>TCA495779820SALL1c.3345C>A (p.Ser1115=)
c.3054C>A (p.Ser1018=)
c.77-1325C>A (n.77-1325C>A)
16g.51138878G>ACA395880595SALL1c.3344C>T (p.Ser1115Phe)
c.3053C>T (p.Ser1018Phe)
c.77-1326C>T (n.77-1326C>T)
16g.51138878G>CCA395880597SALL1c.3344C>G (p.Ser1115Cys)
c.3053C>G (p.Ser1018Cys)
c.77-1326C>G (n.77-1326C>G)
16g.51138878G>TCA395880598SALL1c.3344C>A (p.Ser1115Tyr)
c.3053C>A (p.Ser1018Tyr)
c.77-1326C>A (n.77-1326C>A)
16g.51138879A>CCA395880608SALL1c.3343T>G (p.Ser1115Ala)
c.3052T>G (p.Ser1018Ala)
c.77-1327T>G (n.77-1327T>G)
16g.51138879A>GCA395880605SALL1c.3343T>C (p.Ser1115Pro)
c.3052T>C (p.Ser1018Pro)
c.77-1327T>C (n.77-1327T>C)
 gnomAD v4
16g.51138879A>TCA395880602SALL1c.3343T>A (p.Ser1115Thr)
c.3052T>A (p.Ser1018Thr)
c.77-1327T>A (n.77-1327T>A)
16g.51138880A>CCA495779824SALL1c.3342T>G (p.Ser1114=)
c.3051T>G (p.Ser1017=)
c.77-1328T>G (n.77-1328T>G)
 COSMIC
16g.51138880A>GCA495779826SALL1c.3342T>C (p.Ser1114=)
c.3051T>C (p.Ser1017=)
c.77-1328T>C (n.77-1328T>C)
16g.51138880A>TCA495779827SALL1c.3342T>A (p.Ser1114=)
c.3051T>A (p.Ser1017=)
c.77-1328T>A (n.77-1328T>A)
16g.51138881G>ACA395880611SALL1c.3341C>T (p.Ser1114Phe)
c.3050C>T (p.Ser1017Phe)
c.77-1329C>T (n.77-1329C>T)
16g.51138881G>CCA395880616SALL1c.3341C>G (p.Ser1114Cys)
c.3050C>G (p.Ser1017Cys)
c.77-1329C>G (n.77-1329C>G)
16g.51138881G>TCA395880614SALL1c.3341C>A (p.Ser1114Tyr)
c.3050C>A (p.Ser1017Tyr)
c.77-1329C>A (n.77-1329C>A)
 gnomAD v4
16g.51138882A>CCA395880618SALL1c.3340T>G (p.Ser1114Ala)
c.3049T>G (p.Ser1017Ala)
c.77-1330T>G (n.77-1330T>G)
16g.51138882A>GCA395880621SALL1c.3340T>C (p.Ser1114Pro)
c.3049T>C (p.Ser1017Pro)
c.77-1330T>C (n.77-1330T>C)
16g.51138882A>TCA395880620SALL1c.3340T>A (p.Ser1114Thr)
c.3049T>A (p.Ser1017Thr)
c.77-1330T>A (n.77-1330T>A)
16g.51138883C>ACA495779828SALL1c.3339G>T (p.Leu1113=)
c.3048G>T (p.Leu1016=)
c.77-1331G>T (n.77-1331G>T)
16g.51138883C>GCA495779829SALL1c.3339G>C (p.Leu1113=)
c.3048G>C (p.Leu1016=)
c.77-1331G>C (n.77-1331G>C)
16g.51138883C>TCA495779830SALL1c.3339G>A (p.Leu1113=)
c.3048G>A (p.Leu1016=)
c.77-1331G>A (n.77-1331G>A)
16g.51138884A=CA2222016934SALL1c.3338T= (p.Leu1113=)
c.3047T= (p.Leu1016=)
c.77-1332T= (n.77-1332T=)
16g.51138884A>CCA395880624SALL1c.3338T>G (p.Leu1113Arg)
c.3047T>G (p.Leu1016Arg)
c.77-1332T>G (n.77-1332T>G)
16g.51138884A>GCA395880626SALL1c.3338T>C (p.Leu1113Pro)
c.3047T>C (p.Leu1016Pro)
c.77-1332T>C (n.77-1332T>C)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.51138884A>TCA395880628SALL1c.3338T>A (p.Leu1113Gln)
c.3047T>A (p.Leu1016Gln)
c.77-1332T>A (n.77-1332T>A)
 dbSNP gnomAD v2 gnomAD v4
16g.51138885G>ACA495779834SALL1c.3337C>T (p.Leu1113=)
c.3046C>T (p.Leu1016=)
c.77-1333C>T (n.77-1333C>T)
16g.51138885G>CCA395880630SALL1c.3337C>G (p.Leu1113Val)
c.3046C>G (p.Leu1016Val)
c.77-1333C>G (n.77-1333C>G)
 gnomAD v4
16g.51138885G>TCA395880631SALL1c.3337C>A (p.Leu1113Met)
c.3046C>A (p.Leu1016Met)
c.77-1333C>A (n.77-1333C>A)
16g.51138886delCA2695223339SALL1c.3336del (p.Leu1113CysfsTer?)
c.3045del (p.Leu1016CysfsTer?)
c.77-1334del (n.77-1334del)
16g.51138886A>CCA495779836SALL1c.3336T>G (p.Pro1112=)
c.3045T>G (p.Pro1015=)
c.77-1334T>G (n.77-1334T>G)
16g.51138886A>GCA495779837SALL1c.3336T>C (p.Pro1112=)
c.3045T>C (p.Pro1015=)
c.77-1334T>C (n.77-1334T>C)
16g.51138886A>TCA495779835SALL1c.3336T>A (p.Pro1112=)
c.3045T>A (p.Pro1015=)
c.77-1334T>A (n.77-1334T>A)
16g.51138887G>ACA8052945SALL1c.3335C>T (p.Pro1112Leu)
c.3044C>T (p.Pro1015Leu)
c.77-1335C>T (n.77-1335C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138887G>CCA395880637SALL1c.3335C>G (p.Pro1112Arg)
c.3044C>G (p.Pro1015Arg)
c.77-1335C>G (n.77-1335C>G)
16g.51138887G=CA2222016939SALL1c.3335C= (p.Pro1112=)
c.3044C= (p.Pro1015=)
c.77-1335C= (n.77-1335C=)
16g.51138887G>TCA395880639SALL1c.3335C>A (p.Pro1112His)
c.3044C>A (p.Pro1015His)
c.77-1335C>A (n.77-1335C>A)
16g.51138888delCA495779838SALL1c.3335del (p.Pro1112LeufsTer?)
c.3044del (p.Pro1015LeufsTer?)
c.77-1335del (n.77-1335del)
 COSMIC
16g.51138888G>ACA395880643SALL1c.3334C>T (p.Pro1112Ser)
c.3043C>T (p.Pro1015Ser)
c.77-1336C>T (n.77-1336C>T)
16g.51138888G>CCA395880646SALL1c.3334C>G (p.Pro1112Ala)
c.3043C>G (p.Pro1015Ala)
c.77-1336C>G (n.77-1336C>G)
16g.51138888G>TCA395880649SALL1c.3334C>A (p.Pro1112Thr)
c.3043C>A (p.Pro1015Thr)
c.77-1336C>A (n.77-1336C>A)
16g.51138889C>ACA495779841SALL1c.3333G>T (p.Gly1111=)
c.3042G>T (p.Gly1014=)
c.77-1337G>T (n.77-1337G>T)
16g.51138889C=CA2222016949SALL1c.3333G= (p.Gly1111=)
c.3042G= (p.Gly1014=)
c.77-1337G= (n.77-1337G=)
16g.51138889C>GCA8052946SALL1c.3333G>C (p.Gly1111=)
c.3042G>C (p.Gly1014=)
c.77-1337G>C (n.77-1337G>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138889C>TCA8052947SALL1c.3333G>A (p.Gly1111=)
c.3042G>A (p.Gly1014=)
c.77-1337G>A (n.77-1337G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51138890C>ACA395880657SALL1c.3332G>T (p.Gly1111Val)
c.3041G>T (p.Gly1014Val)
c.77-1338G>T (n.77-1338G>T)
16g.51138890C>GCA395880659SALL1c.3332G>C (p.Gly1111Ala)
c.3041G>C (p.Gly1014Ala)
c.77-1338G>C (n.77-1338G>C)
16g.51138890C>TCA395880661SALL1c.3332G>A (p.Gly1111Glu)
c.3041G>A (p.Gly1014Glu)
c.77-1338G>A (n.77-1338G>A)
 gnomAD v4
16g.51138891C>ACA395880663SALL1c.3331G>T (p.Gly1111Trp)
c.3040G>T (p.Gly1014Trp)
c.77-1339G>T (n.77-1339G>T)
16g.51138891C>GCA395880664SALL1c.3331G>C (p.Gly1111Arg)
c.3040G>C (p.Gly1014Arg)
c.77-1339G>C (n.77-1339G>C)
16g.51138891C>TCA395880666SALL1c.3331G>A (p.Gly1111Arg)
c.3040G>A (p.Gly1014Arg)
c.77-1339G>A (n.77-1339G>A)
16g.51138892A=CA2222016952SALL1c.3330T= (p.Ser1110=)
c.3039T= (p.Ser1013=)
c.77-1340T= (n.77-1340T=)
16g.51138892A>CCA495779843SALL1c.3330T>G (p.Ser1110=)
c.3039T>G (p.Ser1013=)
c.77-1340T>G (n.77-1340T>G)
16g.51138892A>GCA8052948SALL1c.3330T>C (p.Ser1110=)
c.3039T>C (p.Ser1013=)
c.77-1340T>C (n.77-1340T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138892A>TCA495779844SALL1c.3330T>A (p.Ser1110=)
c.3039T>A (p.Ser1013=)
c.77-1340T>A (n.77-1340T>A)
16g.51138893G>ACA395880670SALL1c.3329C>T (p.Ser1110Phe)
c.3038C>T (p.Ser1013Phe)
c.77-1341C>T (n.77-1341C>T)
16g.51138893G>CCA395880672SALL1c.3329C>G (p.Ser1110Cys)
c.3038C>G (p.Ser1013Cys)
c.77-1341C>G (n.77-1341C>G)
16g.51138893G>TCA395880675SALL1c.3329C>A (p.Ser1110Tyr)
c.3038C>A (p.Ser1013Tyr)
c.77-1341C>A (n.77-1341C>A)
16g.51138894A=CA2222016957SALL1c.3328T= (p.Ser1110=)
c.3037T= (p.Ser1013=)
c.77-1342T= (n.77-1342T=)
16g.51138894A>CCA395880688SALL1c.3328T>G (p.Ser1110Ala)
c.3037T>G (p.Ser1013Ala)
c.77-1342T>G (n.77-1342T>G)
16g.51138894A>GCA281300611SALL1c.3328T>C (p.Ser1110Pro)
c.3037T>C (p.Ser1013Pro)
c.77-1342T>C (n.77-1342T>C)
 dbSNP
16g.51138894A>TCA395880685SALL1c.3328T>A (p.Ser1110Thr)
c.3037T>A (p.Ser1013Thr)
c.77-1342T>A (n.77-1342T>A)
16g.51138895C>ACA495779846SALL1c.3327G>T (p.Pro1109=)
c.3036G>T (p.Pro1012=)
c.77-1343G>T (n.77-1343G>T)
 gnomAD v4
16g.51138895C=CA2222016962SALL1c.3327G= (p.Pro1109=)
c.3036G= (p.Pro1012=)
c.77-1343G= (n.77-1343G=)
16g.51138895C>GCA495779847SALL1c.3327G>C (p.Pro1109=)
c.3036G>C (p.Pro1012=)
c.77-1343G>C (n.77-1343G>C)
16g.51138895C>TCA8052949SALL1c.3327G>A (p.Pro1109=)
c.3036G>A (p.Pro1012=)
c.77-1343G>A (n.77-1343G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138896G>ACA8052950SALL1c.3326C>T (p.Pro1109Leu)
c.3035C>T (p.Pro1012Leu)
c.77-1344C>T (n.77-1344C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.51138896G>CCA395880696SALL1c.3326C>G (p.Pro1109Arg)
c.3035C>G (p.Pro1012Arg)
c.77-1344C>G (n.77-1344C>G)
16g.51138896G=CA2222016969SALL1c.3326C= (p.Pro1109=)
c.3035C= (p.Pro1012=)
c.77-1344C= (n.77-1344C=)
16g.51138896G>TCA395880698SALL1c.3326C>A (p.Pro1109Gln)
c.3035C>A (p.Pro1012Gln)
c.77-1344C>A (n.77-1344C>A)
16g.51138897G>ACA395880706SALL1c.3325C>T (p.Pro1109Ser)
c.3034C>T (p.Pro1012Ser)
c.77-1345C>T (n.77-1345C>T)
 gnomAD v4 COSMIC
16g.51138897G>CCA395880703SALL1c.3325C>G (p.Pro1109Ala)
c.3034C>G (p.Pro1012Ala)
c.77-1345C>G (n.77-1345C>G)
16g.51138897G>TCA395880700SALL1c.3325C>A (p.Pro1109Thr)
c.3034C>A (p.Pro1012Thr)
c.77-1345C>A (n.77-1345C>A)
16g.51138898G>ACA495779849SALL1c.3324C>T (p.Val1108=)
c.3033C>T (p.Val1011=)
c.77-1346C>T (n.77-1346C>T)
16g.51138898G>CCA495779851SALL1c.3324C>G (p.Val1108=)
c.3033C>G (p.Val1011=)
c.77-1346C>G (n.77-1346C>G)
 dbSNP
16g.51138898G>TCA495779852SALL1c.3324C>A (p.Val1108=)
c.3033C>A (p.Val1011=)
c.77-1346C>A (n.77-1346C>A)
16g.51138899A>CCA395880709SALL1c.3323T>G (p.Val1108Gly)
c.3032T>G (p.Val1011Gly)
c.77-1347T>G (n.77-1347T>G)
16g.51138899A>GCA395880711SALL1c.3323T>C (p.Val1108Ala)
c.3032T>C (p.Val1011Ala)
c.77-1347T>C (n.77-1347T>C)
16g.51138899A>TCA395880712SALL1c.3323T>A (p.Val1108Asp)
c.3032T>A (p.Val1011Asp)
c.77-1347T>A (n.77-1347T>A)
16g.51138900C>ACA8052953SALL1c.3322G>T (p.Val1108Phe)
c.3031G>T (p.Val1011Phe)
c.77-1348G>T (n.77-1348G>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.51138900C=CA2222016976SALL1c.3322G= (p.Val1108=)
c.3031G= (p.Val1011=)
c.77-1348G= (n.77-1348G=)
16g.51138900C>GCA8052951SALL1c.3322G>C (p.Val1108Leu)
c.3031G>C (p.Val1011Leu)
c.77-1348G>C (n.77-1348G>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138900C>TCA8052952SALL1c.3322G>A (p.Val1108Ile)
c.3031G>A (p.Val1011Ile)
c.77-1348G>A (n.77-1348G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.51138901G>ACA8052954SALL1c.3321C>T (p.His1107=)
c.3030C>T (p.His1010=)
c.77-1349C>T (n.77-1349C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138901G>CCA395880722SALL1c.3321C>G (p.His1107Gln)
c.3030C>G (p.His1010Gln)
c.77-1349C>G (n.77-1349C>G)
 COSMIC
16g.51138901G=CA2222016988SALL1c.3321C= (p.His1107=)
c.3030C= (p.His1010=)
c.77-1349C= (n.77-1349C=)
16g.51138901G>TCA281300662SALL1c.3321C>A (p.His1107Gln)
c.3030C>A (p.His1010Gln)
c.77-1349C>A (n.77-1349C>A)
 dbSNP gnomAD v3 gnomAD v4
16g.51138902T>ACA395880726SALL1c.3320A>T (p.His1107Leu)
c.3029A>T (p.His1010Leu)
c.77-1350A>T (n.77-1350A>T)
16g.51138902T>CCA395880729SALL1c.3320A>G (p.His1107Arg)
c.3029A>G (p.His1010Arg)
c.77-1350A>G (n.77-1350A>G)
16g.51138902T>GCA395880731SALL1c.3320A>C (p.His1107Pro)
c.3029A>C (p.His1010Pro)
c.77-1350A>C (n.77-1350A>C)
 dbSNP gnomAD v2 gnomAD v4
16g.51138902T=CA2222016995SALL1c.3320A= (p.His1107=)
c.3029A= (p.His1010=)
c.77-1350A= (n.77-1350A=)
16g.51138903G>ACA395880734SALL1c.3319C>T (p.His1107Tyr)
c.3028C>T (p.His1010Tyr)
c.77-1351C>T (n.77-1351C>T)
16g.51138903G>CCA395880744SALL1c.3319C>G (p.His1107Asp)
c.3028C>G (p.His1010Asp)
c.77-1351C>G (n.77-1351C>G)
16g.51138903G>TCA395880747SALL1c.3319C>A (p.His1107Asn)
c.3028C>A (p.His1010Asn)
c.77-1351C>A (n.77-1351C>A)
16g.51138904A>CCA395880748SALL1c.3318T>G (p.Ser1106Arg)
c.3027T>G (p.Ser1009Arg)
c.77-1352T>G (n.77-1352T>G)
16g.51138904A>GCA495779856SALL1c.3318T>C (p.Ser1106=)
c.3027T>C (p.Ser1009=)
c.77-1352T>C (n.77-1352T>C)
16g.51138904A>TCA395880750SALL1c.3318T>A (p.Ser1106Arg)
c.3027T>A (p.Ser1009Arg)
c.77-1352T>A (n.77-1352T>A)
16g.51138905C>ACA395880752SALL1c.3317G>T (p.Ser1106Ile)
c.3026G>T (p.Ser1009Ile)
c.77-1353G>T (n.77-1353G>T)
16g.51138905C=CA2222016999SALL1c.3317G= (p.Ser1106=)
c.3026G= (p.Ser1009=)
c.77-1353G= (n.77-1353G=)
16g.51138905C>GCA395880753SALL1c.3317G>C (p.Ser1106Thr)
c.3026G>C (p.Ser1009Thr)
c.77-1353G>C (n.77-1353G>C)
16g.51138905C>TCA395880754SALL1c.3317G>A (p.Ser1106Asn)
c.3026G>A (p.Ser1009Asn)
c.77-1353G>A (n.77-1353G>A)
 dbSNP
16g.51138906T>ACA395880756SALL1c.3316A>T (p.Ser1106Cys)
c.3025A>T (p.Ser1009Cys)
c.77-1354A>T (n.77-1354A>T)
16g.51138906T>CCA395880758SALL1c.3316A>G (p.Ser1106Gly)
c.3025A>G (p.Ser1009Gly)
c.77-1354A>G (n.77-1354A>G)
16g.51138906T>GCA395880755SALL1c.3316A>C (p.Ser1106Arg)
c.3025A>C (p.Ser1009Arg)
c.77-1354A>C (n.77-1354A>C)
16g.51138907G>ACA495779858SALL1c.3315C>T (p.Thr1105=)
c.3024C>T (p.Thr1008=)
c.77-1355C>T (n.77-1355C>T)
 gnomAD v4
16g.51138907G>CCA495779860SALL1c.3315C>G (p.Thr1105=)
c.3024C>G (p.Thr1008=)
c.77-1355C>G (n.77-1355C>G)
16g.51138907G>TCA495779859SALL1c.3315C>A (p.Thr1105=)
c.3024C>A (p.Thr1008=)
c.77-1355C>A (n.77-1355C>A)
16g.51138908G>ACA395880759SALL1c.3314C>T (p.Thr1105Ile)
c.3023C>T (p.Thr1008Ile)
c.77-1356C>T (n.77-1356C>T)
 gnomAD v4
16g.51138908G>CCA395880761SALL1c.3314C>G (p.Thr1105Ser)
c.3023C>G (p.Thr1008Ser)
c.77-1356C>G (n.77-1356C>G)
16g.51138908G>TCA395880763SALL1c.3314C>A (p.Thr1105Asn)
c.3023C>A (p.Thr1008Asn)
c.77-1356C>A (n.77-1356C>A)
16g.51138909T>ACA395880765SALL1c.3313A>T (p.Thr1105Ser)
c.3022A>T (p.Thr1008Ser)
c.77-1357A>T (n.77-1357A>T)
16g.51138909T>CCA395880767SALL1c.3313A>G (p.Thr1105Ala)
c.3022A>G (p.Thr1008Ala)
c.77-1357A>G (n.77-1357A>G)
16g.51138909T>GCA395880770SALL1c.3313A>C (p.Thr1105Pro)
c.3022A>C (p.Thr1008Pro)
c.77-1357A>C (n.77-1357A>C)
 dbSNP
16g.51138909T=CA2222017008SALL1c.3313A= (p.Thr1105=)
c.3022A= (p.Thr1008=)
c.77-1357A= (n.77-1357A=)
16g.51138910G>ACA495779861SALL1c.3312C>T (p.Pro1104=)
c.3021C>T (p.Pro1007=)
c.77-1358C>T (n.77-1358C>T)
16g.51138910G>CCA495779862SALL1c.3312C>G (p.Pro1104=)
c.3021C>G (p.Pro1007=)
c.77-1358C>G (n.77-1358C>G)
16g.51138910G=CA2222017013SALL1c.3312C= (p.Pro1104=)
c.3021C= (p.Pro1007=)
c.77-1358C= (n.77-1358C=)
16g.51138910G>TCA8052955SALL1c.3312C>A (p.Pro1104=)
c.3021C>A (p.Pro1007=)
c.77-1358C>A (n.77-1358C>A)
 dbSNP ExAC gnomAD v4
16g.51138911G>ACA395880775SALL1c.3311C>T (p.Pro1104Leu)
c.3020C>T (p.Pro1007Leu)
c.77-1359C>T (n.77-1359C>T)
16g.51138911G>CCA395880779SALL1c.3311C>G (p.Pro1104Arg)
c.3020C>G (p.Pro1007Arg)
c.77-1359C>G (n.77-1359C>G)
16g.51138911G>TCA395880777SALL1c.3311C>A (p.Pro1104His)
c.3020C>A (p.Pro1007His)
c.77-1359C>A (n.77-1359C>A)
16g.51138912G>ACA395880783SALL1c.3310C>T (p.Pro1104Ser)
c.3019C>T (p.Pro1007Ser)
c.77-1360C>T (n.77-1360C>T)
 gnomAD v4
16g.51138912G>CCA8052956SALL1c.3310C>G (p.Pro1104Ala)
c.3019C>G (p.Pro1007Ala)
c.77-1360C>G (n.77-1360C>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138912G=CA2222017019SALL1c.3310C= (p.Pro1104=)
c.3019C= (p.Pro1007=)
c.77-1360C= (n.77-1360C=)
16g.51138912G>TCA395880787SALL1c.3310C>A (p.Pro1104Thr)
c.3019C>A (p.Pro1007Thr)
c.77-1360C>A (n.77-1360C>A)
16g.51138913G>ACA495779866SALL1c.3309C>T (p.Thr1103=)
c.3018C>T (p.Thr1006=)
c.77-1361C>T (n.77-1361C>T)
 dbSNP gnomAD v3 gnomAD v4
16g.51138913G>CCA495779867SALL1c.3309C>G (p.Thr1103=)
c.3018C>G (p.Thr1006=)
c.77-1361C>G (n.77-1361C>G)
16g.51138913G=CA2222017026SALL1c.3309C= (p.Thr1103=)
c.3018C= (p.Thr1006=)
c.77-1361C= (n.77-1361C=)
16g.51138913G>TCA8052957SALL1c.3309C>A (p.Thr1103=)
c.3018C>A (p.Thr1006=)
c.77-1361C>A (n.77-1361C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51138914G>ACA395880795SALL1c.3308C>T (p.Thr1103Ile)
c.3017C>T (p.Thr1006Ile)
c.77-1362C>T (n.77-1362C>T)
16g.51138914G>CCA395880791SALL1c.3308C>G (p.Thr1103Ser)
c.3017C>G (p.Thr1006Ser)
c.77-1362C>G (n.77-1362C>G)
16g.51138914G>TCA395880794SALL1c.3308C>A (p.Thr1103Asn)
c.3017C>A (p.Thr1006Asn)
c.77-1362C>A (n.77-1362C>A)
 gnomAD v4
16g.51138915T>ACA395880798SALL1c.3307A>T (p.Thr1103Ser)
c.3016A>T (p.Thr1006Ser)
c.77-1363A>T (n.77-1363A>T)
16g.51138915T>CCA395880801SALL1c.3307A>G (p.Thr1103Ala)
c.3016A>G (p.Thr1006Ala)
c.77-1363A>G (n.77-1363A>G)
16g.51138915T>GCA395880804SALL1c.3307A>C (p.Thr1103Pro)
c.3016A>C (p.Thr1006Pro)
c.77-1363A>C (n.77-1363A>C)
 dbSNP
16g.51138915T=CA2222017035SALL1c.3307A= (p.Thr1103=)
c.3016A= (p.Thr1006=)
c.77-1363A= (n.77-1363A=)
16g.51138916G>ACA495779870SALL1c.3306C>T (p.Asp1102=)
c.3015C>T (p.Asp1005=)
c.77-1364C>T (n.77-1364C>T)
16g.51138916G>CCA395880807SALL1c.3306C>G (p.Asp1102Glu)
c.3015C>G (p.Asp1005Glu)
c.77-1364C>G (n.77-1364C>G)
16g.51138916G>TCA395880810SALL1c.3306C>A (p.Asp1102Glu)
c.3015C>A (p.Asp1005Glu)
c.77-1364C>A (n.77-1364C>A)
 gnomAD v4
16g.51138917T>ACA395880813SALL1c.3305A>T (p.Asp1102Val)
c.3014A>T (p.Asp1005Val)
c.77-1365A>T (n.77-1365A>T)
16g.51138917T>CCA10605926SALL1c.3305A>G (p.Asp1102Gly)
c.3014A>G (p.Asp1005Gly)
c.77-1365A>G (n.77-1365A>G)
 ClinVar dbSNP
16g.51138917T>GCA395880817SALL1c.3305A>C (p.Asp1102Ala)
c.3014A>C (p.Asp1005Ala)
c.77-1365A>C (n.77-1365A>C)
16g.51138917T=CA2222017040SALL1c.3305A= (p.Asp1102=)
c.3014A= (p.Asp1005=)
c.77-1365A= (n.77-1365A=)
16g.51138918C>ACA395880820SALL1c.3304G>T (p.Asp1102Tyr)
c.3013G>T (p.Asp1005Tyr)
c.77-1366G>T (n.77-1366G>T)
16g.51138918C>GCA395880823SALL1c.3304G>C (p.Asp1102His)
c.3013G>C (p.Asp1005His)
c.77-1366G>C (n.77-1366G>C)
16g.51138918C>TCA395880825SALL1c.3304G>A (p.Asp1102Asn)
c.3013G>A (p.Asp1005Asn)
c.77-1366G>A (n.77-1366G>A)
16g.51138919C>ACA395880828SALL1c.3303G>T (p.Lys1101Asn)
c.3012G>T (p.Lys1004Asn)
c.77-1367G>T (n.77-1367G>T)
16g.51138919C>GCA395880830SALL1c.3303G>C (p.Lys1101Asn)
c.3012G>C (p.Lys1004Asn)
c.77-1367G>C (n.77-1367G>C)
16g.51138919C>TCA495779876SALL1c.3303G>A (p.Lys1101=)
c.3012G>A (p.Lys1004=)
c.77-1367G>A (n.77-1367G>A)
16g.51138920T>ACA395880834SALL1c.3302A>T (p.Lys1101Met)
c.3011A>T (p.Lys1004Met)
c.77-1368A>T (n.77-1368A>T)
16g.51138920T>CCA281300686SALL1c.3302A>G (p.Lys1101Arg)
c.3011A>G (p.Lys1004Arg)
c.77-1368A>G (n.77-1368A>G)
 dbSNP
16g.51138920T>GCA395880839SALL1c.3302A>C (p.Lys1101Thr)
c.3011A>C (p.Lys1004Thr)
c.77-1368A>C (n.77-1368A>C)
16g.51138920T=CA2222017048SALL1c.3302A= (p.Lys1101=)
c.3011A= (p.Lys1004=)
c.77-1368A= (n.77-1368A=)
16g.51138921T>ACA395880842SALL1c.3301A>T (p.Lys1101Ter)
c.3010A>T (p.Lys1004Ter)
c.77-1369A>T (n.77-1369A>T)
16g.51138921T>CCA395880844SALL1c.3301A>G (p.Lys1101Glu)
c.3010A>G (p.Lys1004Glu)
c.77-1369A>G (n.77-1369A>G)
 dbSNP gnomAD v2 gnomAD v4
16g.51138921T>GCA395880846SALL1c.3301A>C (p.Lys1101Gln)
c.3010A>C (p.Lys1004Gln)
c.77-1369A>C (n.77-1369A>C)
16g.51138921T=CA2222017051SALL1c.3301A= (p.Lys1101=)
c.3010A= (p.Lys1004=)
c.77-1369A= (n.77-1369A=)
16g.51138922A>CCA395880849SALL1c.3300T>G (p.Ser1100Arg)
c.3009T>G (p.Ser1003Arg)
c.77-1370T>G (n.77-1370T>G)
16g.51138922A>GCA495779879SALL1c.3300T>C (p.Ser1100=)
c.3009T>C (p.Ser1003=)
c.77-1370T>C (n.77-1370T>C)
16g.51138922A>TCA395880851SALL1c.3300T>A (p.Ser1100Arg)
c.3009T>A (p.Ser1003Arg)
c.77-1370T>A (n.77-1370T>A)
16g.51138923C>ACA395880855SALL1c.3299G>T (p.Ser1100Ile)
c.3008G>T (p.Ser1003Ile)
c.77-1371G>T (n.77-1371G>T)
 COSMIC
16g.51138923C>GCA395880857SALL1c.3299G>C (p.Ser1100Thr)
c.3008G>C (p.Ser1003Thr)
c.77-1371G>C (n.77-1371G>C)
16g.51138923C>TCA395880860SALL1c.3299G>A (p.Ser1100Asn)
c.3008G>A (p.Ser1003Asn)
c.77-1371G>A (n.77-1371G>A)
 dbSNP
16g.51138924T>ACA395880863SALL1c.3298A>T (p.Ser1100Cys)
c.3007A>T (p.Ser1003Cys)
c.77-1372A>T (n.77-1372A>T)
 dbSNP
16g.51138924T>CCA395880866SALL1c.3298A>G (p.Ser1100Gly)
c.3007A>G (p.Ser1003Gly)
c.77-1372A>G (n.77-1372A>G)
16g.51138924T>GCA395880868SALL1c.3298A>C (p.Ser1100Arg)
c.3007A>C (p.Ser1003Arg)
c.77-1372A>C (n.77-1372A>C)
16g.51138924T=CA2222017055SALL1c.3298A= (p.Ser1100=)
c.3007A= (p.Ser1003=)
c.77-1372A= (n.77-1372A=)
16g.51138925G>ACA495779883SALL1c.3297C>T (p.Asp1099=)
c.3006C>T (p.Asp1002=)
c.77-1373C>T (n.77-1373C>T)
 dbSNP gnomAD v4
16g.51138925G>CCA8052958SALL1c.3297C>G (p.Asp1099Glu)
c.3006C>G (p.Asp1002Glu)
c.77-1373C>G (n.77-1373C>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51138925G=CA2222017056SALL1c.3297C= (p.Asp1099=)
c.3006C= (p.Asp1002=)
c.77-1373C= (n.77-1373C=)
16g.51138925G>TCA395880874SALL1c.3297C>A (p.Asp1099Glu)
c.3006C>A (p.Asp1002Glu)
c.77-1373C>A (n.77-1373C>A)
16g.51138926T>ACA395880880SALL1c.3296A>T (p.Asp1099Val)
c.3005A>T (p.Asp1002Val)
c.77-1374A>T (n.77-1374A>T)
16g.51138926T>CCA395880875SALL1c.3296A>G (p.Asp1099Gly)
c.3005A>G (p.Asp1002Gly)
c.77-1374A>G (n.77-1374A>G)
16g.51138926T>GCA395880878SALL1c.3296A>C (p.Asp1099Ala)
c.3005A>C (p.Asp1002Ala)
c.77-1374A>C (n.77-1374A>C)
16g.51138927C>ACA395880882SALL1c.3295G>T (p.Asp1099Tyr)
c.3004G>T (p.Asp1002Tyr)
c.77-1375G>T (n.77-1375G>T)
 gnomAD v4
16g.51138927C>GCA395880884SALL1c.3295G>C (p.Asp1099His)
c.3004G>C (p.Asp1002His)
c.77-1375G>C (n.77-1375G>C)
16g.51138927C>TCA395880887SALL1c.3295G>A (p.Asp1099Asn)
c.3004G>A (p.Asp1002Asn)
c.77-1375G>A (n.77-1375G>A)
 gnomAD v4

Number of alleles fetched