Chr Mutation (hg38) CAid Gene Transcript Linkouts
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

Number of alleles fetched