Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.51784289_51784291delCA2577428493SALL4c.3139_3141del (p.Glu1047del)
c.808_810del (p.Glu270del)
c.1828_1830del (p.Glu610del)
c.2833_2835del (p.Glu945del)
c.3013_3015del (p.Glu1005del)
20g.51784288C>ACA409005592SALL4c.3139G>T (p.Glu1047Ter)
c.808G>T (p.Glu270Ter)
c.1828G>T (p.Glu610Ter)
c.2833G>T (p.Glu945Ter)
c.3013G>T (p.Glu1005Ter)
COSMIC
20g.51784288C>GCA409005591SALL4c.3139G>C (p.Glu1047Gln)
c.808G>C (p.Glu270Gln)
c.1828G>C (p.Glu610Gln)
c.2833G>C (p.Glu945Gln)
c.3013G>C (p.Glu1005Gln)
20g.51784288C>TCA409005590SALL4c.3139G>A (p.Glu1047Lys)
c.808G>A (p.Glu270Lys)
c.1828G>A (p.Glu610Lys)
c.2833G>A (p.Glu945Lys)
c.3013G>A (p.Glu1005Lys)
20g.51784289T>ACA409005593SALL4c.3138A>T (p.Glu1046Asp)
c.807A>T (p.Glu269Asp)
c.1827A>T (p.Glu609Asp)
c.2832A>T (p.Glu944Asp)
c.3012A>T (p.Glu1004Asp)
20g.51784289T>CCA511025509SALL4c.3138A>G (p.Glu1046=)
c.807A>G (p.Glu269=)
c.1827A>G (p.Glu609=)
c.2832A>G (p.Glu944=)
c.3012A>G (p.Glu1004=)
20g.51784289T>GCA409005594SALL4c.3138A>C (p.Glu1046Asp)
c.807A>C (p.Glu269Asp)
c.1827A>C (p.Glu609Asp)
c.2832A>C (p.Glu944Asp)
c.3012A>C (p.Glu1004Asp)
20g.51784290T>ACA409005595SALL4c.3137A>T (p.Glu1046Val)
c.806A>T (p.Glu269Val)
c.1826A>T (p.Glu609Val)
c.2831A>T (p.Glu944Val)
c.3011A>T (p.Glu1004Val)
20g.51784290T>CCA409005596SALL4c.3137A>G (p.Glu1046Gly)
c.806A>G (p.Glu269Gly)
c.1826A>G (p.Glu609Gly)
c.2831A>G (p.Glu944Gly)
c.3011A>G (p.Glu1004Gly)
20g.51784290T>GCA409005598SALL4c.3137A>C (p.Glu1046Ala)
c.806A>C (p.Glu269Ala)
c.1826A>C (p.Glu609Ala)
c.2831A>C (p.Glu944Ala)
c.3011A>C (p.Glu1004Ala)
20g.51784291C>ACA409005599SALL4c.3136G>T (p.Glu1046Ter)
c.805G>T (p.Glu269Ter)
c.1825G>T (p.Glu609Ter)
c.2830G>T (p.Glu944Ter)
c.3010G>T (p.Glu1004Ter)
20g.51784291C>GCA409005600SALL4c.3136G>C (p.Glu1046Gln)
c.805G>C (p.Glu269Gln)
c.1825G>C (p.Glu609Gln)
c.2830G>C (p.Glu944Gln)
c.3010G>C (p.Glu1004Gln)
20g.51784291C>TCA409005601SALL4c.3136G>A (p.Glu1046Lys)
c.805G>A (p.Glu269Lys)
c.1825G>A (p.Glu609Lys)
c.2830G>A (p.Glu944Lys)
c.3010G>A (p.Glu1004Lys)
20g.51784292C>ACA511025514SALL4c.3135G>T (p.Leu1045=)
c.804G>T (p.Leu268=)
c.1824G>T (p.Leu608=)
c.2829G>T (p.Leu943=)
c.3009G>T (p.Leu1003=)
20g.51784292C=CA2369155198SALL4c.3135G= (p.Leu1045=)
c.804G= (p.Leu268=)
c.1824G= (p.Leu608=)
c.2829G= (p.Leu943=)
c.3009G= (p.Leu1003=)
20g.51784292C>GCA511025515SALL4c.3135G>C (p.Leu1045=)
c.804G>C (p.Leu268=)
c.1824G>C (p.Leu608=)
c.2829G>C (p.Leu943=)
c.3009G>C (p.Leu1003=)
20g.51784292C>TCA9911914SALL4c.3135G>A (p.Leu1045=)
c.804G>A (p.Leu268=)
c.1824G>A (p.Leu608=)
c.2829G>A (p.Leu943=)
c.3009G>A (p.Leu1003=)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784293A=CA2369155199SALL4c.3134T= (p.Leu1045=)
c.803T= (p.Leu268=)
c.1823T= (p.Leu608=)
c.2828T= (p.Leu943=)
c.3008T= (p.Leu1003=)
20g.51784293A>CCA409005602SALL4c.3134T>G (p.Leu1045Arg)
c.803T>G (p.Leu268Arg)
c.1823T>G (p.Leu608Arg)
c.2828T>G (p.Leu943Arg)
c.3008T>G (p.Leu1003Arg)
20g.51784293A>GCA409005603SALL4c.3134T>C (p.Leu1045Pro)
c.803T>C (p.Leu268Pro)
c.1823T>C (p.Leu608Pro)
c.2828T>C (p.Leu943Pro)
c.3008T>C (p.Leu1003Pro)
dbSNP gnomAD v2 gnomAD v4
20g.51784293A>TCA409005604SALL4c.3134T>A (p.Leu1045Gln)
c.803T>A (p.Leu268Gln)
c.1823T>A (p.Leu608Gln)
c.2828T>A (p.Leu943Gln)
c.3008T>A (p.Leu1003Gln)
20g.51784294G>ACA511025519SALL4c.3133C>T (p.Leu1045=)
c.802C>T (p.Leu268=)
c.1822C>T (p.Leu608=)
c.2827C>T (p.Leu943=)
c.3007C>T (p.Leu1003=)
dbSNP
20g.51784294G>CCA409005606SALL4c.3133C>G (p.Leu1045Val)
c.802C>G (p.Leu268Val)
c.1822C>G (p.Leu608Val)
c.2827C>G (p.Leu943Val)
c.3007C>G (p.Leu1003Val)
20g.51784294G=CA2369155200SALL4c.3133C= (p.Leu1045=)
c.802C= (p.Leu268=)
c.1822C= (p.Leu608=)
c.2827C= (p.Leu943=)
c.3007C= (p.Leu1003=)
20g.51784294G>TCA409005605SALL4c.3133C>A (p.Leu1045Met)
c.802C>A (p.Leu268Met)
c.1822C>A (p.Leu608Met)
c.2827C>A (p.Leu943Met)
c.3007C>A (p.Leu1003Met)
dbSNP gnomAD v3 gnomAD v4
20g.51784295G>ACA511025523SALL4c.3132C>T (p.Phe1044=)
c.801C>T (p.Phe267=)
c.1821C>T (p.Phe607=)
c.2826C>T (p.Phe942=)
c.3006C>T (p.Phe1002=)
20g.51784295G>CCA409005607SALL4c.3132C>G (p.Phe1044Leu)
c.801C>G (p.Phe267Leu)
c.1821C>G (p.Phe607Leu)
c.2826C>G (p.Phe942Leu)
c.3006C>G (p.Phe1002Leu)
20g.51784295G=CA2369155201SALL4c.3132C= (p.Phe1044=)
c.801C= (p.Phe267=)
c.1821C= (p.Phe607=)
c.2826C= (p.Phe942=)
c.3006C= (p.Phe1002=)
20g.51784295G>TCA409005608SALL4c.3132C>A (p.Phe1044Leu)
c.801C>A (p.Phe267Leu)
c.1821C>A (p.Phe607Leu)
c.2826C>A (p.Phe942Leu)
c.3006C>A (p.Phe1002Leu)
dbSNP gnomAD v3 gnomAD v4
20g.51784296A=CA2369155202SALL4c.3131T= (p.Phe1044=)
c.800T= (p.Phe267=)
c.1820T= (p.Phe607=)
c.2825T= (p.Phe942=)
c.3005T= (p.Phe1002=)
20g.51784296A>CCA409005609SALL4c.3131T>G (p.Phe1044Cys)
c.800T>G (p.Phe267Cys)
c.1820T>G (p.Phe607Cys)
c.2825T>G (p.Phe942Cys)
c.3005T>G (p.Phe1002Cys)
20g.51784296A>GCA409005610SALL4c.3131T>C (p.Phe1044Ser)
c.800T>C (p.Phe267Ser)
c.1820T>C (p.Phe607Ser)
c.2825T>C (p.Phe942Ser)
c.3005T>C (p.Phe1002Ser)
gnomAD v4
20g.51784296A>TCA409005611SALL4c.3131T>A (p.Phe1044Tyr)
c.800T>A (p.Phe267Tyr)
c.1820T>A (p.Phe607Tyr)
c.2825T>A (p.Phe942Tyr)
c.3005T>A (p.Phe1002Tyr)
dbSNP
20g.51784297A=CA2369155203SALL4c.3130T= (p.Phe1044=)
c.799T= (p.Phe267=)
c.1819T= (p.Phe607=)
c.2824T= (p.Phe942=)
c.3004T= (p.Phe1002=)
20g.51784297A>CCA409005612SALL4c.3130T>G (p.Phe1044Val)
c.799T>G (p.Phe267Val)
c.1819T>G (p.Phe607Val)
c.2824T>G (p.Phe942Val)
c.3004T>G (p.Phe1002Val)
dbSNP gnomAD v4
20g.51784297A>GCA409005613SALL4c.3130T>C (p.Phe1044Leu)
c.799T>C (p.Phe267Leu)
c.1819T>C (p.Phe607Leu)
c.2824T>C (p.Phe942Leu)
c.3004T>C (p.Phe1002Leu)
dbSNP
20g.51784297A>TCA409005614SALL4c.3130T>A (p.Phe1044Ile)
c.799T>A (p.Phe267Ile)
c.1819T>A (p.Phe607Ile)
c.2824T>A (p.Phe942Ile)
c.3004T>A (p.Phe1002Ile)
dbSNP gnomAD v4
20g.51784298G>ACA511025532SALL4c.3129C>T (p.His1043=)
c.798C>T (p.His266=)
c.1818C>T (p.His606=)
c.2823C>T (p.His941=)
c.3003C>T (p.His1001=)
20g.51784298G>CCA409005615SALL4c.3129C>G (p.His1043Gln)
c.798C>G (p.His266Gln)
c.1818C>G (p.His606Gln)
c.2823C>G (p.His941Gln)
c.3003C>G (p.His1001Gln)
20g.51784298G=CA2369155204SALL4c.3129C= (p.His1043=)
c.798C= (p.His266=)
c.1818C= (p.His606=)
c.2823C= (p.His941=)
c.3003C= (p.His1001=)
20g.51784298G>TCA409005616SALL4c.3129C>A (p.His1043Gln)
c.798C>A (p.His266Gln)
c.1818C>A (p.His606Gln)
c.2823C>A (p.His941Gln)
c.3003C>A (p.His1001Gln)
dbSNP gnomAD v2 gnomAD v4
20g.51784299T>ACA409005617SALL4c.3128A>T (p.His1043Leu)
c.797A>T (p.His266Leu)
c.1817A>T (p.His606Leu)
c.2822A>T (p.His941Leu)
c.3002A>T (p.His1001Leu)
dbSNP gnomAD v3 gnomAD v4
20g.51784299T>CCA409005618SALL4c.3128A>G (p.His1043Arg)
c.797A>G (p.His266Arg)
c.1817A>G (p.His606Arg)
c.2822A>G (p.His941Arg)
c.3002A>G (p.His1001Arg)
20g.51784299T>GCA9911915SALL4c.3128A>C (p.His1043Pro)
c.797A>C (p.His266Pro)
c.1817A>C (p.His606Pro)
c.2822A>C (p.His941Pro)
c.3002A>C (p.His1001Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784299T=CA2369155205SALL4c.3128A= (p.His1043=)
c.797A= (p.His266=)
c.1817A= (p.His606=)
c.2822A= (p.His941=)
c.3002A= (p.His1001=)
20g.51784300G>ACA409005621SALL4c.3127C>T (p.His1043Tyr)
c.796C>T (p.His266Tyr)
c.1816C>T (p.His606Tyr)
c.2821C>T (p.His941Tyr)
c.3001C>T (p.His1001Tyr)
20g.51784300G>CCA409005619SALL4c.3127C>G (p.His1043Asp)
c.796C>G (p.His266Asp)
c.1816C>G (p.His606Asp)
c.2821C>G (p.His941Asp)
c.3001C>G (p.His1001Asp)
20g.51784300G>TCA409005620SALL4c.3127C>A (p.His1043Asn)
c.796C>A (p.His266Asn)
c.1816C>A (p.His606Asn)
c.2821C>A (p.His941Asn)
c.3001C>A (p.His1001Asn)
20g.51784301A>CCA511025544SALL4c.3126T>G (p.Pro1042=)
c.795T>G (p.Pro265=)
c.1815T>G (p.Pro605=)
c.2820T>G (p.Pro940=)
c.3000T>G (p.Pro1000=)
20g.51784301A>GCA511025542SALL4c.3126T>C (p.Pro1042=)
c.795T>C (p.Pro265=)
c.1815T>C (p.Pro605=)
c.2820T>C (p.Pro940=)
c.3000T>C (p.Pro1000=)
20g.51784301A>TCA511025540SALL4c.3126T>A (p.Pro1042=)
c.795T>A (p.Pro265=)
c.1815T>A (p.Pro605=)
c.2820T>A (p.Pro940=)
c.3000T>A (p.Pro1000=)
20g.51784302G>ACA409005622SALL4c.3125C>T (p.Pro1042Leu)
c.794C>T (p.Pro265Leu)
c.1814C>T (p.Pro605Leu)
c.2819C>T (p.Pro940Leu)
c.2999C>T (p.Pro1000Leu)
20g.51784302G>CCA409005623SALL4c.3125C>G (p.Pro1042Arg)
c.794C>G (p.Pro265Arg)
c.1814C>G (p.Pro605Arg)
c.2819C>G (p.Pro940Arg)
c.2999C>G (p.Pro1000Arg)
20g.51784302G>TCA409005624SALL4c.3125C>A (p.Pro1042His)
c.794C>A (p.Pro265His)
c.1814C>A (p.Pro605His)
c.2819C>A (p.Pro940His)
c.2999C>A (p.Pro1000His)
20g.51784303G>ACA409005625SALL4c.3124C>T (p.Pro1042Ser)
c.793C>T (p.Pro265Ser)
c.1813C>T (p.Pro605Ser)
c.2818C>T (p.Pro940Ser)
c.2998C>T (p.Pro1000Ser)
COSMIC
20g.51784303G>CCA409005626SALL4c.3124C>G (p.Pro1042Ala)
c.793C>G (p.Pro265Ala)
c.1813C>G (p.Pro605Ala)
c.2818C>G (p.Pro940Ala)
c.2998C>G (p.Pro1000Ala)
20g.51784303G>TCA409005627SALL4c.3124C>A (p.Pro1042Thr)
c.793C>A (p.Pro265Thr)
c.1813C>A (p.Pro605Thr)
c.2818C>A (p.Pro940Thr)
c.2998C>A (p.Pro1000Thr)
20g.51784304A>CCA409005628SALL4c.3123T>G (p.Phe1041Leu)
c.792T>G (p.Phe264Leu)
c.1812T>G (p.Phe604Leu)
c.2817T>G (p.Phe939Leu)
c.2997T>G (p.Phe999Leu)
20g.51784304A>GCA511025551SALL4c.3123T>C (p.Phe1041=)
c.792T>C (p.Phe264=)
c.1812T>C (p.Phe604=)
c.2817T>C (p.Phe939=)
c.2997T>C (p.Phe999=)
20g.51784304A>TCA409005629SALL4c.3123T>A (p.Phe1041Leu)
c.792T>A (p.Phe264Leu)
c.1812T>A (p.Phe604Leu)
c.2817T>A (p.Phe939Leu)
c.2997T>A (p.Phe999Leu)
20g.51784304_51785229delinsCTAAGGCAGGAGAATCACTTGAACCCAGAATCA645610833SALL4c.2743-545_3123delinsATTCTGGGTTCAAGTGATTCTCCTGCCTTAG
c.412-545_792delinsATTCTGGGTTCAAGTGATTCTCCTGCCTTAG
c.1432-545_1812delinsATTCTGGGTTCAAGTGATTCTCCTGCCTTAG
c.2437-545_2817delinsATTCTGGGTTCAAGTGATTCTCCTGCCTTAG
c.2617-545_2997delinsATTCTGGGTTCAAGTGATTCTCCTGCCTTAG
COSMIC
20g.51784305A>CCA409005630SALL4c.3122T>G (p.Phe1041Cys)
c.791T>G (p.Phe264Cys)
c.1811T>G (p.Phe604Cys)
c.2816T>G (p.Phe939Cys)
c.2996T>G (p.Phe999Cys)
20g.51784305A>GCA409005631SALL4c.3122T>C (p.Phe1041Ser)
c.791T>C (p.Phe264Ser)
c.1811T>C (p.Phe604Ser)
c.2816T>C (p.Phe939Ser)
c.2996T>C (p.Phe999Ser)
20g.51784305A>TCA409005632SALL4c.3122T>A (p.Phe1041Tyr)
c.791T>A (p.Phe264Tyr)
c.1811T>A (p.Phe604Tyr)
c.2816T>A (p.Phe939Tyr)
c.2996T>A (p.Phe999Tyr)
20g.51784306A=CA2369155206SALL4c.3121T= (p.Phe1041=)
c.790T= (p.Phe264=)
c.1810T= (p.Phe604=)
c.2815T= (p.Phe939=)
c.2995T= (p.Phe999=)
20g.51784306A>CCA409005635SALL4c.3121T>G (p.Phe1041Val)
c.790T>G (p.Phe264Val)
c.1810T>G (p.Phe604Val)
c.2815T>G (p.Phe939Val)
c.2995T>G (p.Phe999Val)
20g.51784306A>GCA409005634SALL4c.3121T>C (p.Phe1041Leu)
c.790T>C (p.Phe264Leu)
c.1810T>C (p.Phe604Leu)
c.2815T>C (p.Phe939Leu)
c.2995T>C (p.Phe999Leu)
20g.51784306A>TCA409005633SALL4c.3121T>A (p.Phe1041Ile)
c.790T>A (p.Phe264Ile)
c.1810T>A (p.Phe604Ile)
c.2815T>A (p.Phe939Ile)
c.2995T>A (p.Phe999Ile)
dbSNP
20g.51784307C>ACA409005636SALL4c.3120G>T (p.Gln1040His)
c.789G>T (p.Gln263His)
c.1809G>T (p.Gln603His)
c.2814G>T (p.Gln938His)
c.2994G>T (p.Gln998His)
20g.51784307C=CA2369155207SALL4c.3120G= (p.Gln1040=)
c.789G= (p.Gln263=)
c.1809G= (p.Gln603=)
c.2814G= (p.Gln938=)
c.2994G= (p.Gln998=)
20g.51784307C>GCA409005637SALL4c.3120G>C (p.Gln1040His)
c.789G>C (p.Gln263His)
c.1809G>C (p.Gln603His)
c.2814G>C (p.Gln938His)
c.2994G>C (p.Gln998His)
dbSNP gnomAD v4
20g.51784307C>TCA511025556SALL4c.3120G>A (p.Gln1040=)
c.789G>A (p.Gln263=)
c.1809G>A (p.Gln603=)
c.2814G>A (p.Gln938=)
c.2994G>A (p.Gln998=)
20g.51784308T>ACA409005638SALL4c.3119A>T (p.Gln1040Leu)
c.788A>T (p.Gln263Leu)
c.1808A>T (p.Gln603Leu)
c.2813A>T (p.Gln938Leu)
c.2993A>T (p.Gln998Leu)
20g.51784308T>CCA409005639SALL4c.3119A>G (p.Gln1040Arg)
c.788A>G (p.Gln263Arg)
c.1808A>G (p.Gln603Arg)
c.2813A>G (p.Gln938Arg)
c.2993A>G (p.Gln998Arg)
20g.51784308T>GCA315365628SALL4c.3119A>C (p.Gln1040Pro)
c.788A>C (p.Gln263Pro)
c.1808A>C (p.Gln603Pro)
c.2813A>C (p.Gln938Pro)
c.2993A>C (p.Gln998Pro)
dbSNP
20g.51784308T=CA2369155208SALL4c.3119A= (p.Gln1040=)
c.788A= (p.Gln263=)
c.1808A= (p.Gln603=)
c.2813A= (p.Gln938=)
c.2993A= (p.Gln998=)
20g.51784309G>ACA409005640SALL4c.3118C>T (p.Gln1040Ter)
c.787C>T (p.Gln263Ter)
c.1807C>T (p.Gln603Ter)
c.2812C>T (p.Gln938Ter)
c.2992C>T (p.Gln998Ter)
20g.51784309G>CCA409005641SALL4c.3118C>G (p.Gln1040Glu)
c.787C>G (p.Gln263Glu)
c.1807C>G (p.Gln603Glu)
c.2812C>G (p.Gln938Glu)
c.2992C>G (p.Gln998Glu)
20g.51784309G>TCA409005642SALL4c.3118C>A (p.Gln1040Lys)
c.787C>A (p.Gln263Lys)
c.1807C>A (p.Gln603Lys)
c.2812C>A (p.Gln938Lys)
c.2992C>A (p.Gln998Lys)
20g.51784310G>ACA511025562SALL4c.3117C>T (p.His1039=)
c.786C>T (p.His262=)
c.1806C>T (p.His602=)
c.2811C>T (p.His937=)
c.2991C>T (p.His997=)
gnomAD v4
20g.51784310G>CCA409005643SALL4c.3117C>G (p.His1039Gln)
c.786C>G (p.His262Gln)
c.1806C>G (p.His602Gln)
c.2811C>G (p.His937Gln)
c.2991C>G (p.His997Gln)
20g.51784310G>TCA409005644SALL4c.3117C>A (p.His1039Gln)
c.786C>A (p.His262Gln)
c.1806C>A (p.His602Gln)
c.2811C>A (p.His937Gln)
c.2991C>A (p.His997Gln)
20g.51784311T>ACA409005645SALL4c.3116A>T (p.His1039Leu)
c.785A>T (p.His262Leu)
c.1805A>T (p.His602Leu)
c.2810A>T (p.His937Leu)
c.2990A>T (p.His997Leu)
20g.51784311T>CCA409005646SALL4c.3116A>G (p.His1039Arg)
c.785A>G (p.His262Arg)
c.1805A>G (p.His602Arg)
c.2810A>G (p.His937Arg)
c.2990A>G (p.His997Arg)
20g.51784311T>GCA409005647SALL4c.3116A>C (p.His1039Pro)
c.785A>C (p.His262Pro)
c.1805A>C (p.His602Pro)
c.2810A>C (p.His937Pro)
c.2990A>C (p.His997Pro)
20g.51784312G>ACA409005650SALL4c.3115C>T (p.His1039Tyr)
c.784C>T (p.His262Tyr)
c.1804C>T (p.His602Tyr)
c.2809C>T (p.His937Tyr)
c.2989C>T (p.His997Tyr)
gnomAD v4
20g.51784312G>CCA409005648SALL4c.3115C>G (p.His1039Asp)
c.784C>G (p.His262Asp)
c.1804C>G (p.His602Asp)
c.2809C>G (p.His937Asp)
c.2989C>G (p.His997Asp)
20g.51784312G>TCA409005649SALL4c.3115C>A (p.His1039Asn)
c.784C>A (p.His262Asn)
c.1804C>A (p.His602Asn)
c.2809C>A (p.His937Asn)
c.2989C>A (p.His997Asn)
20g.51784313T>ACA409005651SALL4c.3114A>T (p.Lys1038Asn)
c.783A>T (p.Lys261Asn)
c.1803A>T (p.Lys601Asn)
c.2808A>T (p.Lys936Asn)
c.2988A>T (p.Lys996Asn)
20g.51784313T>CCA511025569SALL4c.3114A>G (p.Lys1038=)
c.783A>G (p.Lys261=)
c.1803A>G (p.Lys601=)
c.2808A>G (p.Lys936=)
c.2988A>G (p.Lys996=)
dbSNP
20g.51784313T>GCA409005652SALL4c.3114A>C (p.Lys1038Asn)
c.783A>C (p.Lys261Asn)
c.1803A>C (p.Lys601Asn)
c.2808A>C (p.Lys936Asn)
c.2988A>C (p.Lys996Asn)
20g.51784313T=CA2369155209SALL4c.3114A= (p.Lys1038=)
c.783A= (p.Lys261=)
c.1803A= (p.Lys601=)
c.2808A= (p.Lys936=)
c.2988A= (p.Lys996=)
20g.51784314T>ACA409005653SALL4c.3113A>T (p.Lys1038Ile)
c.782A>T (p.Lys261Ile)
c.1802A>T (p.Lys601Ile)
c.2807A>T (p.Lys936Ile)
c.2987A>T (p.Lys996Ile)
20g.51784314T>CCA409005654SALL4c.3113A>G (p.Lys1038Arg)
c.782A>G (p.Lys261Arg)
c.1802A>G (p.Lys601Arg)
c.2807A>G (p.Lys936Arg)
c.2987A>G (p.Lys996Arg)
gnomAD v4
20g.51784314T>GCA409005655SALL4c.3113A>C (p.Lys1038Thr)
c.782A>C (p.Lys261Thr)
c.1802A>C (p.Lys601Thr)
c.2807A>C (p.Lys936Thr)
c.2987A>C (p.Lys996Thr)
20g.51784315T>ACA409005656SALL4c.3112A>T (p.Lys1038Ter)
c.781A>T (p.Lys261Ter)
c.1801A>T (p.Lys601Ter)
c.2806A>T (p.Lys936Ter)
c.2986A>T (p.Lys996Ter)
20g.51784315T>CCA409005657SALL4c.3112A>G (p.Lys1038Glu)
c.781A>G (p.Lys261Glu)
c.1801A>G (p.Lys601Glu)
c.2806A>G (p.Lys936Glu)
c.2986A>G (p.Lys996Glu)
20g.51784315T>GCA409005658SALL4c.3112A>C (p.Lys1038Gln)
c.781A>C (p.Lys261Gln)
c.1801A>C (p.Lys601Gln)
c.2806A>C (p.Lys936Gln)
c.2986A>C (p.Lys996Gln)
gnomAD v4
20g.51784316G>ACA511025574SALL4c.3111C>T (p.Pro1037=)
c.780C>T (p.Pro260=)
c.1800C>T (p.Pro600=)
c.2805C>T (p.Pro935=)
c.2985C>T (p.Pro995=)
dbSNP
20g.51784316G>CCA511025576SALL4c.3111C>G (p.Pro1037=)
c.780C>G (p.Pro260=)
c.1800C>G (p.Pro600=)
c.2805C>G (p.Pro935=)
c.2985C>G (p.Pro995=)
20g.51784316G=CA2369155210SALL4c.3111C= (p.Pro1037=)
c.780C= (p.Pro260=)
c.1800C= (p.Pro600=)
c.2805C= (p.Pro935=)
c.2985C= (p.Pro995=)
20g.51784316G>TCA511025578SALL4c.3111C>A (p.Pro1037=)
c.780C>A (p.Pro260=)
c.1800C>A (p.Pro600=)
c.2805C>A (p.Pro935=)
c.2985C>A (p.Pro995=)
20g.51784317G>ACA409005659SALL4c.3110C>T (p.Pro1037Leu)
c.779C>T (p.Pro260Leu)
c.1799C>T (p.Pro600Leu)
c.2804C>T (p.Pro935Leu)
c.2984C>T (p.Pro995Leu)
COSMIC
20g.51784317G>CCA409005660SALL4c.3110C>G (p.Pro1037Arg)
c.779C>G (p.Pro260Arg)
c.1799C>G (p.Pro600Arg)
c.2804C>G (p.Pro935Arg)
c.2984C>G (p.Pro995Arg)
gnomAD v4
20g.51784317G>TCA409005661SALL4c.3110C>A (p.Pro1037His)
c.779C>A (p.Pro260His)
c.1799C>A (p.Pro600His)
c.2804C>A (p.Pro935His)
c.2984C>A (p.Pro995His)
20g.51784318G>ACA315365632SALL4c.3109C>T (p.Pro1037Ser)
c.778C>T (p.Pro260Ser)
c.1798C>T (p.Pro600Ser)
c.2803C>T (p.Pro935Ser)
c.2983C>T (p.Pro995Ser)
dbSNP
20g.51784318G>CCA409005663SALL4c.3109C>G (p.Pro1037Ala)
c.778C>G (p.Pro260Ala)
c.1798C>G (p.Pro600Ala)
c.2803C>G (p.Pro935Ala)
c.2983C>G (p.Pro995Ala)
20g.51784318G=CA2369155211SALL4c.3109C= (p.Pro1037=)
c.778C= (p.Pro260=)
c.1798C= (p.Pro600=)
c.2803C= (p.Pro935=)
c.2983C= (p.Pro995=)
20g.51784318G>TCA409005662SALL4c.3109C>A (p.Pro1037Thr)
c.778C>A (p.Pro260Thr)
c.1798C>A (p.Pro600Thr)
c.2803C>A (p.Pro935Thr)
c.2983C>A (p.Pro995Thr)
gnomAD v4
20g.51784319A>CCA511025587SALL4c.3108T>G (p.Val1036=)
c.777T>G (p.Val259=)
c.1797T>G (p.Val599=)
c.2802T>G (p.Val934=)
c.2982T>G (p.Val994=)
20g.51784319A>GCA511025589SALL4c.3108T>C (p.Val1036=)
c.777T>C (p.Val259=)
c.1797T>C (p.Val599=)
c.2802T>C (p.Val934=)
c.2982T>C (p.Val994=)
20g.51784319A>TCA511025588SALL4c.3108T>A (p.Val1036=)
c.777T>A (p.Val259=)
c.1797T>A (p.Val599=)
c.2802T>A (p.Val934=)
c.2982T>A (p.Val994=)
20g.51784320A>CCA409005664SALL4c.3107T>G (p.Val1036Gly)
c.776T>G (p.Val259Gly)
c.1796T>G (p.Val599Gly)
c.2801T>G (p.Val934Gly)
c.2981T>G (p.Val994Gly)
20g.51784320A>GCA409005665SALL4c.3107T>C (p.Val1036Ala)
c.776T>C (p.Val259Ala)
c.1796T>C (p.Val599Ala)
c.2801T>C (p.Val934Ala)
c.2981T>C (p.Val994Ala)
20g.51784320A>TCA409005666SALL4c.3107T>A (p.Val1036Asp)
c.776T>A (p.Val259Asp)
c.1796T>A (p.Val599Asp)
c.2801T>A (p.Val934Asp)
c.2981T>A (p.Val994Asp)
20g.51784321C>ACA409005667SALL4c.3106G>T (p.Val1036Phe)
c.775G>T (p.Val259Phe)
c.1795G>T (p.Val599Phe)
c.2800G>T (p.Val934Phe)
c.2980G>T (p.Val994Phe)
20g.51784321C=CA2369155212SALL4c.3106G= (p.Val1036=)
c.775G= (p.Val259=)
c.1795G= (p.Val599=)
c.2800G= (p.Val934=)
c.2980G= (p.Val994=)
20g.51784321C>GCA409005668SALL4c.3106G>C (p.Val1036Leu)
c.775G>C (p.Val259Leu)
c.1795G>C (p.Val599Leu)
c.2800G>C (p.Val934Leu)
c.2980G>C (p.Val994Leu)
20g.51784321C>TCA9911916SALL4c.3106G>A (p.Val1036Ile)
c.775G>A (p.Val259Ile)
c.1795G>A (p.Val599Ile)
c.2800G>A (p.Val934Ile)
c.2980G>A (p.Val994Ile)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.51784322G>ACA9911917SALL4c.3105C>T (p.Gly1035=)
c.774C>T (p.Gly258=)
c.1794C>T (p.Gly598=)
c.2799C>T (p.Gly933=)
c.2979C>T (p.Gly993=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.51784322G>CCA9911918SALL4c.3105C>G (p.Gly1035=)
c.774C>G (p.Gly258=)
c.1794C>G (p.Gly598=)
c.2799C>G (p.Gly933=)
c.2979C>G (p.Gly993=)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
20g.51784322G=CA2369155213SALL4c.3105C= (p.Gly1035=)
c.774C= (p.Gly258=)
c.1794C= (p.Gly598=)
c.2799C= (p.Gly933=)
c.2979C= (p.Gly993=)
20g.51784322G>TCA511025598SALL4c.3105C>A (p.Gly1035=)
c.774C>A (p.Gly258=)
c.1794C>A (p.Gly598=)
c.2799C>A (p.Gly933=)
c.2979C>A (p.Gly993=)
20g.51784323C>ACA409005669SALL4c.3104G>T (p.Gly1035Val)
c.773G>T (p.Gly258Val)
c.1793G>T (p.Gly598Val)
c.2798G>T (p.Gly933Val)
c.2978G>T (p.Gly993Val)
20g.51784323C=CA2369155214SALL4c.3104G= (p.Gly1035=)
c.773G= (p.Gly258=)
c.1793G= (p.Gly598=)
c.2798G= (p.Gly933=)
c.2978G= (p.Gly993=)
20g.51784323C>GCA409005670SALL4c.3104G>C (p.Gly1035Ala)
c.773G>C (p.Gly258Ala)
c.1793G>C (p.Gly598Ala)
c.2798G>C (p.Gly933Ala)
c.2978G>C (p.Gly993Ala)
20g.51784323C>TCA409005671SALL4c.3104G>A (p.Gly1035Asp)
c.773G>A (p.Gly258Asp)
c.1793G>A (p.Gly598Asp)
c.2798G>A (p.Gly933Asp)
c.2978G>A (p.Gly993Asp)
dbSNP gnomAD v3 gnomAD v4
20g.51784324C>ACA409005672SALL4c.3103G>T (p.Gly1035Cys)
c.772G>T (p.Gly258Cys)
c.1792G>T (p.Gly598Cys)
c.2797G>T (p.Gly933Cys)
c.2977G>T (p.Gly993Cys)
gnomAD v4
20g.51784324C=CA2369155215SALL4c.3103G= (p.Gly1035=)
c.772G= (p.Gly258=)
c.1792G= (p.Gly598=)
c.2797G= (p.Gly933=)
c.2977G= (p.Gly993=)
20g.51784324C>GCA409005673SALL4c.3103G>C (p.Gly1035Arg)
c.772G>C (p.Gly258Arg)
c.1792G>C (p.Gly598Arg)
c.2797G>C (p.Gly933Arg)
c.2977G>C (p.Gly993Arg)
gnomAD v4
20g.51784324C>TCA9911919SALL4c.3103G>A (p.Gly1035Ser)
c.772G>A (p.Gly258Ser)
c.1792G>A (p.Gly598Ser)
c.2797G>A (p.Gly933Ser)
c.2977G>A (p.Gly993Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.51784325G>ACA9911920SALL4c.3102C>T (p.Asp1034=)
c.771C>T (p.Asp257=)
c.1791C>T (p.Asp597=)
c.2796C>T (p.Asp932=)
c.2976C>T (p.Asp992=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.51784325G>CCA409005675SALL4c.3102C>G (p.Asp1034Glu)
c.771C>G (p.Asp257Glu)
c.1791C>G (p.Asp597Glu)
c.2796C>G (p.Asp932Glu)
c.2976C>G (p.Asp992Glu)
dbSNP
20g.51784325G=CA2369155216SALL4c.3102C= (p.Asp1034=)
c.771C= (p.Asp257=)
c.1791C= (p.Asp597=)
c.2796C= (p.Asp932=)
c.2976C= (p.Asp992=)
20g.51784325G>TCA409005674SALL4c.3102C>A (p.Asp1034Glu)
c.771C>A (p.Asp257Glu)
c.1791C>A (p.Asp597Glu)
c.2796C>A (p.Asp932Glu)
c.2976C>A (p.Asp992Glu)
20g.51784326T>ACA409005676SALL4c.3101A>T (p.Asp1034Val)
c.770A>T (p.Asp257Val)
c.1790A>T (p.Asp597Val)
c.2795A>T (p.Asp932Val)
c.2975A>T (p.Asp992Val)
20g.51784326T>CCA409005677SALL4c.3101A>G (p.Asp1034Gly)
c.770A>G (p.Asp257Gly)
c.1790A>G (p.Asp597Gly)
c.2795A>G (p.Asp932Gly)
c.2975A>G (p.Asp992Gly)
20g.51784326T>GCA409005678SALL4c.3101A>C (p.Asp1034Ala)
c.770A>C (p.Asp257Ala)
c.1790A>C (p.Asp597Ala)
c.2795A>C (p.Asp932Ala)
c.2975A>C (p.Asp992Ala)
20g.51784327C>ACA409005679SALL4c.3100G>T (p.Asp1034Tyr)
c.769G>T (p.Asp257Tyr)
c.1789G>T (p.Asp597Tyr)
c.2794G>T (p.Asp932Tyr)
c.2974G>T (p.Asp992Tyr)
20g.51784327C=CA2369155217SALL4c.3100G= (p.Asp1034=)
c.769G= (p.Asp257=)
c.1789G= (p.Asp597=)
c.2794G= (p.Asp932=)
c.2974G= (p.Asp992=)
20g.51784327C>GCA409005680SALL4c.3100G>C (p.Asp1034His)
c.769G>C (p.Asp257His)
c.1789G>C (p.Asp597His)
c.2794G>C (p.Asp932His)
c.2974G>C (p.Asp992His)
20g.51784327C>TCA409005681SALL4c.3100G>A (p.Asp1034Asn)
c.769G>A (p.Asp257Asn)
c.1789G>A (p.Asp597Asn)
c.2794G>A (p.Asp932Asn)
c.2974G>A (p.Asp992Asn)
20g.51784328A>CCA511025610SALL4c.3099T>G (p.Thr1033=)
c.768T>G (p.Thr256=)
c.1788T>G (p.Thr596=)
c.2793T>G (p.Thr931=)
c.2973T>G (p.Thr991=)
20g.51784328A>GCA511025611SALL4c.3099T>C (p.Thr1033=)
c.768T>C (p.Thr256=)
c.1788T>C (p.Thr596=)
c.2793T>C (p.Thr931=)
c.2973T>C (p.Thr991=)
20g.51784328A>TCA511025612SALL4c.3099T>A (p.Thr1033=)
c.768T>A (p.Thr256=)
c.1788T>A (p.Thr596=)
c.2793T>A (p.Thr931=)
c.2973T>A (p.Thr991=)
20g.51784328dupCA2369155218SALL4c.3099dup (p.Asp1034Ter)
c.768dup (p.Asp257Ter)
c.1788dup (p.Asp597Ter)
c.2793dup (p.Asp932Ter)
c.2973dup (p.Asp992Ter)
dbSNP
20g.51784329G>ACA315365687SALL4c.3098C>T (p.Thr1033Ile)
c.767C>T (p.Thr256Ile)
c.1787C>T (p.Thr596Ile)
c.2792C>T (p.Thr931Ile)
c.2972C>T (p.Thr991Ile)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.51784329G>CCA409005682SALL4c.3098C>G (p.Thr1033Ser)
c.767C>G (p.Thr256Ser)
c.1787C>G (p.Thr596Ser)
c.2792C>G (p.Thr931Ser)
c.2972C>G (p.Thr991Ser)
20g.51784329G=CA2369155219SALL4c.3098C= (p.Thr1033=)
c.767C= (p.Thr256=)
c.1787C= (p.Thr596=)
c.2792C= (p.Thr931=)
c.2972C= (p.Thr991=)
20g.51784329G>TCA409005683SALL4c.3098C>A (p.Thr1033Asn)
c.767C>A (p.Thr256Asn)
c.1787C>A (p.Thr596Asn)
c.2792C>A (p.Thr931Asn)
c.2972C>A (p.Thr991Asn)
20g.51784330T>ACA409005684SALL4c.3097A>T (p.Thr1033Ser)
c.766A>T (p.Thr256Ser)
c.1786A>T (p.Thr596Ser)
c.2791A>T (p.Thr931Ser)
c.2971A>T (p.Thr991Ser)
20g.51784330T>CCA315365693SALL4c.3097A>G (p.Thr1033Ala)
c.766A>G (p.Thr256Ala)
c.1786A>G (p.Thr596Ala)
c.2791A>G (p.Thr931Ala)
c.2971A>G (p.Thr991Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.51784330T>GCA409005685SALL4c.3097A>C (p.Thr1033Pro)
c.766A>C (p.Thr256Pro)
c.1786A>C (p.Thr596Pro)
c.2791A>C (p.Thr931Pro)
c.2971A>C (p.Thr991Pro)
20g.51784330T=CA2369155220SALL4c.3097A= (p.Thr1033=)
c.766A= (p.Thr256=)
c.1786A= (p.Thr596=)
c.2791A= (p.Thr931=)
c.2971A= (p.Thr991=)
20g.51784331A=CA2369155221SALL4c.3096T= (p.Ala1032=)
c.765T= (p.Ala255=)
c.1785T= (p.Ala595=)
c.2790T= (p.Ala930=)
c.2970T= (p.Ala990=)
20g.51784331A>CCA511025616SALL4c.3096T>G (p.Ala1032=)
c.765T>G (p.Ala255=)
c.1785T>G (p.Ala595=)
c.2790T>G (p.Ala930=)
c.2970T>G (p.Ala990=)
20g.51784331A>GCA9911921SALL4c.3096T>C (p.Ala1032=)
c.765T>C (p.Ala255=)
c.1785T>C (p.Ala595=)
c.2790T>C (p.Ala930=)
c.2970T>C (p.Ala990=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.51784331A>TCA511025617SALL4c.3096T>A (p.Ala1032=)
c.765T>A (p.Ala255=)
c.1785T>A (p.Ala595=)
c.2790T>A (p.Ala930=)
c.2970T>A (p.Ala990=)
20g.51784332G>ACA409005687SALL4c.3095C>T (p.Ala1032Val)
c.764C>T (p.Ala255Val)
c.1784C>T (p.Ala595Val)
c.2789C>T (p.Ala930Val)
c.2969C>T (p.Ala990Val)
dbSNP gnomAD v2 gnomAD v4
20g.51784332G>CCA409005686SALL4c.3095C>G (p.Ala1032Gly)
c.764C>G (p.Ala255Gly)
c.1784C>G (p.Ala595Gly)
c.2789C>G (p.Ala930Gly)
c.2969C>G (p.Ala990Gly)
20g.51784332G=CA2369155222SALL4c.3095C= (p.Ala1032=)
c.764C= (p.Ala255=)
c.1784C= (p.Ala595=)
c.2789C= (p.Ala930=)
c.2969C= (p.Ala990=)
20g.51784332G>TCA409005688SALL4c.3095C>A (p.Ala1032Asp)
c.764C>A (p.Ala255Asp)
c.1784C>A (p.Ala595Asp)
c.2789C>A (p.Ala930Asp)
c.2969C>A (p.Ala990Asp)
20g.51784333C>ACA409005689SALL4c.3094G>T (p.Ala1032Ser)
c.763G>T (p.Ala255Ser)
c.1783G>T (p.Ala595Ser)
c.2788G>T (p.Ala930Ser)
c.2968G>T (p.Ala990Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.51784333C=CA2369155223SALL4c.3094G= (p.Ala1032=)
c.763G= (p.Ala255=)
c.1783G= (p.Ala595=)
c.2788G= (p.Ala930=)
c.2968G= (p.Ala990=)
20g.51784333C>GCA409005691SALL4c.3094G>C (p.Ala1032Pro)
c.763G>C (p.Ala255Pro)
c.1783G>C (p.Ala595Pro)
c.2788G>C (p.Ala930Pro)
c.2968G>C (p.Ala990Pro)
20g.51784333C>TCA409005690SALL4c.3094G>A (p.Ala1032Thr)
c.763G>A (p.Ala255Thr)
c.1783G>A (p.Ala595Thr)
c.2788G>A (p.Ala930Thr)
c.2968G>A (p.Ala990Thr)
gnomAD v4
20g.51784334A=CA2369155224SALL4c.3093T= (p.Ser1031=)
c.762T= (p.Ser254=)
c.1782T= (p.Ser594=)
c.2787T= (p.Ser929=)
c.2967T= (p.Ser989=)
20g.51784334A>CCA409005692SALL4c.3093T>G (p.Ser1031Arg)
c.762T>G (p.Ser254Arg)
c.1782T>G (p.Ser594Arg)
c.2787T>G (p.Ser929Arg)
c.2967T>G (p.Ser989Arg)
dbSNP gnomAD v4
20g.51784334A>GCA511025621SALL4c.3093T>C (p.Ser1031=)
c.762T>C (p.Ser254=)
c.1782T>C (p.Ser594=)
c.2787T>C (p.Ser929=)
c.2967T>C (p.Ser989=)
dbSNP gnomAD v2 gnomAD v4
20g.51784334A>TCA409005693SALL4c.3093T>A (p.Ser1031Arg)
c.762T>A (p.Ser254Arg)
c.1782T>A (p.Ser594Arg)
c.2787T>A (p.Ser929Arg)
c.2967T>A (p.Ser989Arg)
gnomAD v4
20g.51784335C>ACA409005694SALL4c.3092G>T (p.Ser1031Ile)
c.761G>T (p.Ser254Ile)
c.1781G>T (p.Ser594Ile)
c.2786G>T (p.Ser929Ile)
c.2966G>T (p.Ser989Ile)
20g.51784335C>GCA409005695SALL4c.3092G>C (p.Ser1031Thr)
c.761G>C (p.Ser254Thr)
c.1781G>C (p.Ser594Thr)
c.2786G>C (p.Ser929Thr)
c.2966G>C (p.Ser989Thr)
20g.51784335C>TCA409005696SALL4c.3092G>A (p.Ser1031Asn)
c.761G>A (p.Ser254Asn)
c.1781G>A (p.Ser594Asn)
c.2786G>A (p.Ser929Asn)
c.2966G>A (p.Ser989Asn)
20g.51784336T>ACA409005697SALL4c.3091A>T (p.Ser1031Cys)
c.760A>T (p.Ser254Cys)
c.1780A>T (p.Ser594Cys)
c.2785A>T (p.Ser929Cys)
c.2965A>T (p.Ser989Cys)
20g.51784336T>CCA409005698SALL4c.3091A>G (p.Ser1031Gly)
c.760A>G (p.Ser254Gly)
c.1780A>G (p.Ser594Gly)
c.2785A>G (p.Ser929Gly)
c.2965A>G (p.Ser989Gly)
gnomAD v4
20g.51784336T>GCA409005699SALL4c.3091A>C (p.Ser1031Arg)
c.760A>C (p.Ser254Arg)
c.1780A>C (p.Ser594Arg)
c.2785A>C (p.Ser929Arg)
c.2965A>C (p.Ser989Arg)
20g.51784337T>ACA511025624SALL4c.3090A>T (p.Pro1030=)
c.759A>T (p.Pro253=)
c.1779A>T (p.Pro593=)
c.2784A>T (p.Pro928=)
c.2964A>T (p.Pro988=)
20g.51784337T>CCA511025625SALL4c.3090A>G (p.Pro1030=)
c.759A>G (p.Pro253=)
c.1779A>G (p.Pro593=)
c.2784A>G (p.Pro928=)
c.2964A>G (p.Pro988=)
20g.51784337T>GCA511025626SALL4c.3090A>C (p.Pro1030=)
c.759A>C (p.Pro253=)
c.1779A>C (p.Pro593=)
c.2784A>C (p.Pro928=)
c.2964A>C (p.Pro988=)
20g.51784338G>ACA409005700SALL4c.3089C>T (p.Pro1030Leu)
c.758C>T (p.Pro253Leu)
c.1778C>T (p.Pro593Leu)
c.2783C>T (p.Pro928Leu)
c.2963C>T (p.Pro988Leu)
20g.51784338G>CCA409005701SALL4c.3089C>G (p.Pro1030Arg)
c.758C>G (p.Pro253Arg)
c.1778C>G (p.Pro593Arg)
c.2783C>G (p.Pro928Arg)
c.2963C>G (p.Pro988Arg)
20g.51784338G>TCA409005702SALL4c.3089C>A (p.Pro1030Gln)
c.758C>A (p.Pro253Gln)
c.1778C>A (p.Pro593Gln)
c.2783C>A (p.Pro928Gln)
c.2963C>A (p.Pro988Gln)
20g.51784339dupCA2653358750SALL4c.3089dup (p.Ser1031LysfsTer4)
c.758dup (p.Ser254LysfsTer4)
c.1778dup (p.Ser594LysfsTer4)
c.2783dup (p.Ser929LysfsTer4)
c.2963dup (p.Ser989LysfsTer4)
gnomAD v4
20g.51784339G>ACA409005705SALL4c.3088C>T (p.Pro1030Ser)
c.757C>T (p.Pro253Ser)
c.1777C>T (p.Pro593Ser)
c.2782C>T (p.Pro928Ser)
c.2962C>T (p.Pro988Ser)
20g.51784339G>CCA409005703SALL4c.3088C>G (p.Pro1030Ala)
c.757C>G (p.Pro253Ala)
c.1777C>G (p.Pro593Ala)
c.2782C>G (p.Pro928Ala)
c.2962C>G (p.Pro988Ala)
20g.51784339G>TCA409005704SALL4c.3088C>A (p.Pro1030Thr)
c.757C>A (p.Pro253Thr)
c.1777C>A (p.Pro593Thr)
c.2782C>A (p.Pro928Thr)
c.2962C>A (p.Pro988Thr)
20g.51784340T>ACA409005706SALL4c.3087A>T (p.Lys1029Asn)
c.756A>T (p.Lys252Asn)
c.1776A>T (p.Lys592Asn)
c.2781A>T (p.Lys927Asn)
c.2961A>T (p.Lys987Asn)
20g.51784340T>CCA511025628SALL4c.3087A>G (p.Lys1029=)
c.756A>G (p.Lys252=)
c.1776A>G (p.Lys592=)
c.2781A>G (p.Lys927=)
c.2961A>G (p.Lys987=)
20g.51784340T>GCA9911922SALL4c.3087A>C (p.Lys1029Asn)
c.756A>C (p.Lys252Asn)
c.1776A>C (p.Lys592Asn)
c.2781A>C (p.Lys927Asn)
c.2961A>C (p.Lys987Asn)
dbSNP ExAC gnomAD v2
20g.51784340T=CA2369155225SALL4c.3087A= (p.Lys1029=)
c.756A= (p.Lys252=)
c.1776A= (p.Lys592=)
c.2781A= (p.Lys927=)
c.2961A= (p.Lys987=)
20g.51784341T>ACA409005707SALL4c.3086A>T (p.Lys1029Ile)
c.755A>T (p.Lys252Ile)
c.1775A>T (p.Lys592Ile)
c.2780A>T (p.Lys927Ile)
c.2960A>T (p.Lys987Ile)
20g.51784341T>CCA409005708SALL4c.3086A>G (p.Lys1029Arg)
c.755A>G (p.Lys252Arg)
c.1775A>G (p.Lys592Arg)
c.2780A>G (p.Lys927Arg)
c.2960A>G (p.Lys987Arg)
20g.51784341T>GCA409005709SALL4c.3086A>C (p.Lys1029Thr)
c.755A>C (p.Lys252Thr)
c.1775A>C (p.Lys592Thr)
c.2780A>C (p.Lys927Thr)
c.2960A>C (p.Lys987Thr)
20g.51784342T>ACA409005710SALL4c.3085A>T (p.Lys1029Ter)
c.754A>T (p.Lys252Ter)
c.1774A>T (p.Lys592Ter)
c.2779A>T (p.Lys927Ter)
c.2959A>T (p.Lys987Ter)
20g.51784342T>CCA409005711SALL4c.3085A>G (p.Lys1029Glu)
c.754A>G (p.Lys252Glu)
c.1774A>G (p.Lys592Glu)
c.2779A>G (p.Lys927Glu)
c.2959A>G (p.Lys987Glu)
gnomAD v4
20g.51784342T>GCA409005712SALL4c.3085A>C (p.Lys1029Gln)
c.754A>C (p.Lys252Gln)
c.1774A>C (p.Lys592Gln)
c.2779A>C (p.Lys927Gln)
c.2959A>C (p.Lys987Gln)
20g.51784343T>ACA409005713SALL4c.3084A>T (p.Glu1028Asp)
c.753A>T (p.Glu251Asp)
c.1773A>T (p.Glu591Asp)
c.2778A>T (p.Glu926Asp)
c.2958A>T (p.Glu986Asp)
20g.51784343T>CCA511025630SALL4c.3084A>G (p.Glu1028=)
c.753A>G (p.Glu251=)
c.1773A>G (p.Glu591=)
c.2778A>G (p.Glu926=)
c.2958A>G (p.Glu986=)
gnomAD v4
20g.51784343T>GCA409005714SALL4c.3084A>C (p.Glu1028Asp)
c.753A>C (p.Glu251Asp)
c.1773A>C (p.Glu591Asp)
c.2778A>C (p.Glu926Asp)
c.2958A>C (p.Glu986Asp)
20g.51784344T>ACA409005716SALL4c.3083A>T (p.Glu1028Val)
c.752A>T (p.Glu251Val)
c.1772A>T (p.Glu591Val)
c.2777A>T (p.Glu926Val)
c.2957A>T (p.Glu986Val)
20g.51784344T>CCA315365717SALL4c.3083A>G (p.Glu1028Gly)
c.752A>G (p.Glu251Gly)
c.1772A>G (p.Glu591Gly)
c.2777A>G (p.Glu926Gly)
c.2957A>G (p.Glu986Gly)
dbSNP gnomAD v4
20g.51784344T>GCA409005715SALL4c.3083A>C (p.Glu1028Ala)
c.752A>C (p.Glu251Ala)
c.1772A>C (p.Glu591Ala)
c.2777A>C (p.Glu926Ala)
c.2957A>C (p.Glu986Ala)
20g.51784344T=CA2369155226SALL4c.3083A= (p.Glu1028=)
c.752A= (p.Glu251=)
c.1772A= (p.Glu591=)
c.2777A= (p.Glu926=)
c.2957A= (p.Glu986=)
20g.51784345C>ACA409005717SALL4c.3082G>T (p.Glu1028Ter)
c.751G>T (p.Glu251Ter)
c.1771G>T (p.Glu591Ter)
c.2776G>T (p.Glu926Ter)
c.2956G>T (p.Glu986Ter)
COSMIC
20g.51784345C=CA2369155227SALL4c.3082G= (p.Glu1028=)
c.751G= (p.Glu251=)
c.1771G= (p.Glu591=)
c.2776G= (p.Glu926=)
c.2956G= (p.Glu986=)
20g.51784345C>GCA9911923SALL4c.3082G>C (p.Glu1028Gln)
c.751G>C (p.Glu251Gln)
c.1771G>C (p.Glu591Gln)
c.2776G>C (p.Glu926Gln)
c.2956G>C (p.Glu986Gln)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784345C>TCA315365740SALL4c.3082G>A (p.Glu1028Lys)
c.751G>A (p.Glu251Lys)
c.1771G>A (p.Glu591Lys)
c.2776G>A (p.Glu926Lys)
c.2956G>A (p.Glu986Lys)
dbSNP gnomAD v4
20g.51784346C>ACA511025634SALL4c.3081G>T (p.Val1027=)
c.750G>T (p.Val250=)
c.1770G>T (p.Val590=)
c.2775G>T (p.Val925=)
c.2955G>T (p.Val985=)
20g.51784346C=CA2369155228SALL4c.3081G= (p.Val1027=)
c.750G= (p.Val250=)
c.1770G= (p.Val590=)
c.2775G= (p.Val925=)
c.2955G= (p.Val985=)
20g.51784346C>GCA9911925SALL4c.3081G>C (p.Val1027=)
c.750G>C (p.Val250=)
c.1770G>C (p.Val590=)
c.2775G>C (p.Val925=)
c.2955G>C (p.Val985=)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784346C>TCA9911924SALL4c.3081G>A (p.Val1027=)
c.750G>A (p.Val250=)
c.1770G>A (p.Val590=)
c.2775G>A (p.Val925=)
c.2955G>A (p.Val985=)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784347A=CA2369155229SALL4c.3080T= (p.Val1027=)
c.749T= (p.Val250=)
c.1769T= (p.Val590=)
c.2774T= (p.Val925=)
c.2954T= (p.Val985=)
20g.51784347A>CCA9911926SALL4c.3080T>G (p.Val1027Gly)
c.749T>G (p.Val250Gly)
c.1769T>G (p.Val590Gly)
c.2774T>G (p.Val925Gly)
c.2954T>G (p.Val985Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.51784347A>GCA409005718SALL4c.3080T>C (p.Val1027Ala)
c.749T>C (p.Val250Ala)
c.1769T>C (p.Val590Ala)
c.2774T>C (p.Val925Ala)
c.2954T>C (p.Val985Ala)
COSMIC
20g.51784347A>TCA409005719SALL4c.3080T>A (p.Val1027Glu)
c.749T>A (p.Val250Glu)
c.1769T>A (p.Val590Glu)
c.2774T>A (p.Val925Glu)
c.2954T>A (p.Val985Glu)
20g.51784348C>ACA409005720SALL4c.3079G>T (p.Val1027Leu)
c.748G>T (p.Val250Leu)
c.1768G>T (p.Val590Leu)
c.2773G>T (p.Val925Leu)
c.2953G>T (p.Val985Leu)
20g.51784348C>GCA409005721SALL4c.3079G>C (p.Val1027Leu)
c.748G>C (p.Val250Leu)
c.1768G>C (p.Val590Leu)
c.2773G>C (p.Val925Leu)
c.2953G>C (p.Val985Leu)
20g.51784348C>TCA409005722SALL4c.3079G>A (p.Val1027Met)
c.748G>A (p.Val250Met)
c.1768G>A (p.Val590Met)
c.2773G>A (p.Val925Met)
c.2953G>A (p.Val985Met)
20g.51784349A>CCA409005723SALL4c.3078T>G (p.Asp1026Glu)
c.747T>G (p.Asp249Glu)
c.1767T>G (p.Asp589Glu)
c.2772T>G (p.Asp924Glu)
c.2952T>G (p.Asp984Glu)
20g.51784349A>GCA511025637SALL4c.3078T>C (p.Asp1026=)
c.747T>C (p.Asp249=)
c.1767T>C (p.Asp589=)
c.2772T>C (p.Asp924=)
c.2952T>C (p.Asp984=)
gnomAD v4
20g.51784349A>TCA409005724SALL4c.3078T>A (p.Asp1026Glu)
c.747T>A (p.Asp249Glu)
c.1767T>A (p.Asp589Glu)
c.2772T>A (p.Asp924Glu)
c.2952T>A (p.Asp984Glu)
20g.51784350T>ACA409005725SALL4c.3077A>T (p.Asp1026Val)
c.746A>T (p.Asp249Val)
c.1766A>T (p.Asp589Val)
c.2771A>T (p.Asp924Val)
c.2951A>T (p.Asp984Val)
20g.51784350T>CCA409005727SALL4c.3077A>G (p.Asp1026Gly)
c.746A>G (p.Asp249Gly)
c.1766A>G (p.Asp589Gly)
c.2771A>G (p.Asp924Gly)
c.2951A>G (p.Asp984Gly)
20g.51784350T>GCA409005726SALL4c.3077A>C (p.Asp1026Ala)
c.746A>C (p.Asp249Ala)
c.1766A>C (p.Asp589Ala)
c.2771A>C (p.Asp924Ala)
c.2951A>C (p.Asp984Ala)
20g.51784351C>ACA409005728SALL4c.3076G>T (p.Asp1026Tyr)
c.745G>T (p.Asp249Tyr)
c.1765G>T (p.Asp589Tyr)
c.2770G>T (p.Asp924Tyr)
c.2950G>T (p.Asp984Tyr)
dbSNP gnomAD v2 gnomAD v4
20g.51784351C=CA2369155230SALL4c.3076G= (p.Asp1026=)
c.745G= (p.Asp249=)
c.1765G= (p.Asp589=)
c.2770G= (p.Asp924=)
c.2950G= (p.Asp984=)
20g.51784351C>GCA409005729SALL4c.3076G>C (p.Asp1026His)
c.745G>C (p.Asp249His)
c.1765G>C (p.Asp589His)
c.2770G>C (p.Asp924His)
c.2950G>C (p.Asp984His)
20g.51784351C>TCA409005730SALL4c.3076G>A (p.Asp1026Asn)
c.745G>A (p.Asp249Asn)
c.1765G>A (p.Asp589Asn)
c.2770G>A (p.Asp924Asn)
c.2950G>A (p.Asp984Asn)
20g.51784352T>ACA511025638SALL4c.3075A>T (p.Ala1025=)
c.744A>T (p.Ala248=)
c.1764A>T (p.Ala588=)
c.2769A>T (p.Ala923=)
c.2949A>T (p.Ala983=)
20g.51784352T>CCA9911927SALL4c.3075A>G (p.Ala1025=)
c.744A>G (p.Ala248=)
c.1764A>G (p.Ala588=)
c.2769A>G (p.Ala923=)
c.2949A>G (p.Ala983=)
dbSNP ExAC gnomAD v3 gnomAD v4
20g.51784352T>GCA511025639SALL4c.3075A>C (p.Ala1025=)
c.744A>C (p.Ala248=)
c.1764A>C (p.Ala588=)
c.2769A>C (p.Ala923=)
c.2949A>C (p.Ala983=)
20g.51784352T=CA2369155231SALL4c.3075A= (p.Ala1025=)
c.744A= (p.Ala248=)
c.1764A= (p.Ala588=)
c.2769A= (p.Ala923=)
c.2949A= (p.Ala983=)
20g.51784353G>ACA409005731SALL4c.3074C>T (p.Ala1025Val)
c.743C>T (p.Ala248Val)
c.1763C>T (p.Ala588Val)
c.2768C>T (p.Ala923Val)
c.2948C>T (p.Ala983Val)
20g.51784353G>CCA409005732SALL4c.3074C>G (p.Ala1025Gly)
c.743C>G (p.Ala248Gly)
c.1763C>G (p.Ala588Gly)
c.2768C>G (p.Ala923Gly)
c.2948C>G (p.Ala983Gly)
20g.51784353G=CA2369155232SALL4c.3074C= (p.Ala1025=)
c.743C= (p.Ala248=)
c.1763C= (p.Ala588=)
c.2768C= (p.Ala923=)
c.2948C= (p.Ala983=)
20g.51784353G>TCA409005733SALL4c.3074C>A (p.Ala1025Glu)
c.743C>A (p.Ala248Glu)
c.1763C>A (p.Ala588Glu)
c.2768C>A (p.Ala923Glu)
c.2948C>A (p.Ala983Glu)
dbSNP
20g.51784354C>ACA409005734SALL4c.3073G>T (p.Ala1025Ser)
c.742G>T (p.Ala248Ser)
c.1762G>T (p.Ala588Ser)
c.2767G>T (p.Ala923Ser)
c.2947G>T (p.Ala983Ser)
20g.51784354C>GCA409005735SALL4c.3073G>C (p.Ala1025Pro)
c.742G>C (p.Ala248Pro)
c.1762G>C (p.Ala588Pro)
c.2767G>C (p.Ala923Pro)
c.2947G>C (p.Ala983Pro)
20g.51784354C>TCA409005736SALL4c.3073G>A (p.Ala1025Thr)
c.742G>A (p.Ala248Thr)
c.1762G>A (p.Ala588Thr)
c.2767G>A (p.Ala923Thr)
c.2947G>A (p.Ala983Thr)
20g.51784355A=CA2369155233SALL4c.3072T= (p.Ser1024=)
c.741T= (p.Ser247=)
c.1761T= (p.Ser587=)
c.2766T= (p.Ser922=)
c.2946T= (p.Ser982=)
20g.51784355A>CCA409005737SALL4c.3072T>G (p.Ser1024Arg)
c.741T>G (p.Ser247Arg)
c.1761T>G (p.Ser587Arg)
c.2766T>G (p.Ser922Arg)
c.2946T>G (p.Ser982Arg)
20g.51784355A>GCA511025643SALL4c.3072T>C (p.Ser1024=)
c.741T>C (p.Ser247=)
c.1761T>C (p.Ser587=)
c.2766T>C (p.Ser922=)
c.2946T>C (p.Ser982=)
20g.51784355A>TCA9911928SALL4c.3072T>A (p.Ser1024Arg)
c.741T>A (p.Ser247Arg)
c.1761T>A (p.Ser587Arg)
c.2766T>A (p.Ser922Arg)
c.2946T>A (p.Ser982Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784356C>ACA315365765SALL4c.3071G>T (p.Ser1024Ile)
c.740G>T (p.Ser247Ile)
c.1760G>T (p.Ser587Ile)
c.2765G>T (p.Ser922Ile)
c.2945G>T (p.Ser982Ile)
dbSNP
20g.51784356C=CA2369155234SALL4c.3071G= (p.Ser1024=)
c.740G= (p.Ser247=)
c.1760G= (p.Ser587=)
c.2765G= (p.Ser922=)
c.2945G= (p.Ser982=)
20g.51784356C>GCA409005739SALL4c.3071G>C (p.Ser1024Thr)
c.740G>C (p.Ser247Thr)
c.1760G>C (p.Ser587Thr)
c.2765G>C (p.Ser922Thr)
c.2945G>C (p.Ser982Thr)
20g.51784356C>TCA409005738SALL4c.3071G>A (p.Ser1024Asn)
c.740G>A (p.Ser247Asn)
c.1760G>A (p.Ser587Asn)
c.2765G>A (p.Ser922Asn)
c.2945G>A (p.Ser982Asn)
20g.51784357T>ACA409005740SALL4c.3070A>T (p.Ser1024Cys)
c.739A>T (p.Ser247Cys)
c.1759A>T (p.Ser587Cys)
c.2764A>T (p.Ser922Cys)
c.2944A>T (p.Ser982Cys)
20g.51784357T>CCA409005741SALL4c.3070A>G (p.Ser1024Gly)
c.739A>G (p.Ser247Gly)
c.1759A>G (p.Ser587Gly)
c.2764A>G (p.Ser922Gly)
c.2944A>G (p.Ser982Gly)
20g.51784357T>GCA409005742SALL4c.3070A>C (p.Ser1024Arg)
c.739A>C (p.Ser247Arg)
c.1759A>C (p.Ser587Arg)
c.2764A>C (p.Ser922Arg)
c.2944A>C (p.Ser982Arg)
20g.51784358G>ACA9911929SALL4c.3069C>T (p.Ile1023=)
c.738C>T (p.Ile246=)
c.1758C>T (p.Ile586=)
c.2763C>T (p.Ile921=)
c.2943C>T (p.Ile981=)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784358G>CCA409005743SALL4c.3069C>G (p.Ile1023Met)
c.738C>G (p.Ile246Met)
c.1758C>G (p.Ile586Met)
c.2763C>G (p.Ile921Met)
c.2943C>G (p.Ile981Met)
20g.51784358G=CA2369155235SALL4c.3069C= (p.Ile1023=)
c.738C= (p.Ile246=)
c.1758C= (p.Ile586=)
c.2763C= (p.Ile921=)
c.2943C= (p.Ile981=)
20g.51784358G>TCA9911930SALL4c.3069C>A (p.Ile1023=)
c.738C>A (p.Ile246=)
c.1758C>A (p.Ile586=)
c.2763C>A (p.Ile921=)
c.2943C>A (p.Ile981=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.51784359A=CA2369155236SALL4c.3068T= (p.Ile1023=)
c.737T= (p.Ile246=)
c.1757T= (p.Ile586=)
c.2762T= (p.Ile921=)
c.2942T= (p.Ile981=)
20g.51784359A>CCA409005746SALL4c.3068T>G (p.Ile1023Ser)
c.737T>G (p.Ile246Ser)
c.1757T>G (p.Ile586Ser)
c.2762T>G (p.Ile921Ser)
c.2942T>G (p.Ile981Ser)
20g.51784359A>GCA409005744SALL4c.3068T>C (p.Ile1023Thr)
c.737T>C (p.Ile246Thr)
c.1757T>C (p.Ile586Thr)
c.2762T>C (p.Ile921Thr)
c.2942T>C (p.Ile981Thr)
dbSNP gnomAD v3 gnomAD v4
20g.51784359A>TCA409005745SALL4c.3068T>A (p.Ile1023Asn)
c.737T>A (p.Ile246Asn)
c.1757T>A (p.Ile586Asn)
c.2762T>A (p.Ile921Asn)
c.2942T>A (p.Ile981Asn)
20g.51784360T>ACA409005747SALL4c.3067A>T (p.Ile1023Phe)
c.736A>T (p.Ile246Phe)
c.1756A>T (p.Ile586Phe)
c.2761A>T (p.Ile921Phe)
c.2941A>T (p.Ile981Phe)
dbSNP
20g.51784360T>CCA409005748SALL4c.3067A>G (p.Ile1023Val)
c.736A>G (p.Ile246Val)
c.1756A>G (p.Ile586Val)
c.2761A>G (p.Ile921Val)
c.2941A>G (p.Ile981Val)
dbSNP gnomAD v4
20g.51784360T>GCA409005749SALL4c.3067A>C (p.Ile1023Leu)
c.736A>C (p.Ile246Leu)
c.1756A>C (p.Ile586Leu)
c.2761A>C (p.Ile921Leu)
c.2941A>C (p.Ile981Leu)
20g.51784360T=CA2369155237SALL4c.3067A= (p.Ile1023=)
c.736A= (p.Ile246=)
c.1756A= (p.Ile586=)
c.2761A= (p.Ile921=)
c.2941A= (p.Ile981=)
20g.51784361A>CCA511025650SALL4c.3066T>G (p.Gly1022=)
c.735T>G (p.Gly245=)
c.1755T>G (p.Gly585=)
c.2760T>G (p.Gly920=)
c.2940T>G (p.Gly980=)
20g.51784361A>GCA511025651SALL4c.3066T>C (p.Gly1022=)
c.735T>C (p.Gly245=)
c.1755T>C (p.Gly585=)
c.2760T>C (p.Gly920=)
c.2940T>C (p.Gly980=)
20g.51784361A>TCA511025649SALL4c.3066T>A (p.Gly1022=)
c.735T>A (p.Gly245=)
c.1755T>A (p.Gly585=)
c.2760T>A (p.Gly920=)
c.2940T>A (p.Gly980=)
gnomAD v4
20g.51784362C>ACA409005750SALL4c.3065G>T (p.Gly1022Val)
c.734G>T (p.Gly245Val)
c.1754G>T (p.Gly585Val)
c.2759G>T (p.Gly920Val)
c.2939G>T (p.Gly980Val)
gnomAD v4
20g.51784362C=CA2369155238SALL4c.3065G= (p.Gly1022=)
c.734G= (p.Gly245=)
c.1754G= (p.Gly585=)
c.2759G= (p.Gly920=)
c.2939G= (p.Gly980=)
20g.51784362C>GCA315365790SALL4c.3065G>C (p.Gly1022Ala)
c.734G>C (p.Gly245Ala)
c.1754G>C (p.Gly585Ala)
c.2759G>C (p.Gly920Ala)
c.2939G>C (p.Gly980Ala)
dbSNP gnomAD v4
20g.51784362C>TCA409005751SALL4c.3065G>A (p.Gly1022Asp)
c.734G>A (p.Gly245Asp)
c.1754G>A (p.Gly585Asp)
c.2759G>A (p.Gly920Asp)
c.2939G>A (p.Gly980Asp)
dbSNP
20g.51784363C>ACA409005752SALL4c.3064G>T (p.Gly1022Cys)
c.733G>T (p.Gly245Cys)
c.1753G>T (p.Gly585Cys)
c.2758G>T (p.Gly920Cys)
c.2938G>T (p.Gly980Cys)
20g.51784363C=CA2369155239SALL4c.3064G= (p.Gly1022=)
c.733G= (p.Gly245=)
c.1753G= (p.Gly585=)
c.2758G= (p.Gly920=)
c.2938G= (p.Gly980=)
20g.51784363C>GCA9911931SALL4c.3064G>C (p.Gly1022Arg)
c.733G>C (p.Gly245Arg)
c.1753G>C (p.Gly585Arg)
c.2758G>C (p.Gly920Arg)
c.2938G>C (p.Gly980Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.51784363C>TCA409005753SALL4c.3064G>A (p.Gly1022Ser)
c.733G>A (p.Gly245Ser)
c.1753G>A (p.Gly585Ser)
c.2758G>A (p.Gly920Ser)
c.2938G>A (p.Gly980Ser)
20g.51784364C>ACA511025655SALL4c.3063G>T (p.Ser1021=)
c.732G>T (p.Ser244=)
c.1752G>T (p.Ser584=)
c.2757G>T (p.Ser919=)
c.2937G>T (p.Ser979=)
20g.51784364C=CA2369155240SALL4c.3063G= (p.Ser1021=)
c.732G= (p.Ser244=)
c.1752G= (p.Ser584=)
c.2757G= (p.Ser919=)
c.2937G= (p.Ser979=)
20g.51784364C>GCA511025656SALL4c.3063G>C (p.Ser1021=)
c.732G>C (p.Ser244=)
c.1752G>C (p.Ser584=)
c.2757G>C (p.Ser919=)
c.2937G>C (p.Ser979=)
20g.51784364C>TCA9911932SALL4c.3063G>A (p.Ser1021=)
c.732G>A (p.Ser244=)
c.1752G>A (p.Ser584=)
c.2757G>A (p.Ser919=)
c.2937G>A (p.Ser979=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.51784365G>ACA9911933SALL4c.3062C>T (p.Ser1021Leu)
c.731C>T (p.Ser244Leu)
c.1751C>T (p.Ser584Leu)
c.2756C>T (p.Ser919Leu)
c.2936C>T (p.Ser979Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.51784365G>CCA409005754SALL4c.3062C>G (p.Ser1021Trp)
c.731C>G (p.Ser244Trp)
c.1751C>G (p.Ser584Trp)
c.2756C>G (p.Ser919Trp)
c.2936C>G (p.Ser979Trp)
20g.51784365G=CA2369155241SALL4c.3062C= (p.Ser1021=)
c.731C= (p.Ser244=)
c.1751C= (p.Ser584=)
c.2756C= (p.Ser919=)
c.2936C= (p.Ser979=)
20g.51784365G>TCA409005755SALL4c.3062C>A (p.Ser1021Ter)
c.731C>A (p.Ser244Ter)
c.1751C>A (p.Ser584Ter)
c.2756C>A (p.Ser919Ter)
c.2936C>A (p.Ser979Ter)
20g.51784366A>CCA409005756SALL4c.3061T>G (p.Ser1021Ala)
c.730T>G (p.Ser244Ala)
c.1750T>G (p.Ser584Ala)
c.2755T>G (p.Ser919Ala)
c.2935T>G (p.Ser979Ala)
20g.51784366A>GCA409005757SALL4c.3061T>C (p.Ser1021Pro)
c.730T>C (p.Ser244Pro)
c.1750T>C (p.Ser584Pro)
c.2755T>C (p.Ser919Pro)
c.2935T>C (p.Ser979Pro)
20g.51784366A>TCA409005758SALL4c.3061T>A (p.Ser1021Thr)
c.730T>A (p.Ser244Thr)
c.1750T>A (p.Ser584Thr)
c.2755T>A (p.Ser919Thr)
c.2935T>A (p.Ser979Thr)
20g.51784367delCA2695229962SALL4c.3060del (p.Gln1020HisfsTer?)
c.729del (p.Gln243HisfsTer?)
c.1749del (p.Gln583HisfsTer?)
c.2754del (p.Gln918HisfsTer?)
c.2934del (p.Gln978HisfsTer?)
20g.51784367C>ACA409005759SALL4c.3060G>T (p.Gln1020His)
c.729G>T (p.Gln243His)
c.1749G>T (p.Gln583His)
c.2754G>T (p.Gln918His)
c.2934G>T (p.Gln978His)
gnomAD v4
20g.51784367C>GCA409005760SALL4c.3060G>C (p.Gln1020His)
c.729G>C (p.Gln243His)
c.1749G>C (p.Gln583His)
c.2754G>C (p.Gln918His)
c.2934G>C (p.Gln978His)
20g.51784367C>TCA511025658SALL4c.3060G>A (p.Gln1020=)
c.729G>A (p.Gln243=)
c.1749G>A (p.Gln583=)
c.2754G>A (p.Gln918=)
c.2934G>A (p.Gln978=)
20g.51784368T>ACA409005761SALL4c.3059A>T (p.Gln1020Leu)
c.728A>T (p.Gln243Leu)
c.1748A>T (p.Gln583Leu)
c.2753A>T (p.Gln918Leu)
c.2933A>T (p.Gln978Leu)
20g.51784368T>CCA409005762SALL4c.3059A>G (p.Gln1020Arg)
c.728A>G (p.Gln243Arg)
c.1748A>G (p.Gln583Arg)
c.2753A>G (p.Gln918Arg)
c.2933A>G (p.Gln978Arg)
gnomAD v4
20g.51784368T>GCA409005763SALL4c.3059A>C (p.Gln1020Pro)
c.728A>C (p.Gln243Pro)
c.1748A>C (p.Gln583Pro)
c.2753A>C (p.Gln918Pro)
c.2933A>C (p.Gln978Pro)
20g.51784369G>ACA409005764SALL4c.3058C>T (p.Gln1020Ter)
c.727C>T (p.Gln243Ter)
c.1747C>T (p.Gln583Ter)
c.2752C>T (p.Gln918Ter)
c.2932C>T (p.Gln978Ter)
20g.51784369G>CCA409005766SALL4c.3058C>G (p.Gln1020Glu)
c.727C>G (p.Gln243Glu)
c.1747C>G (p.Gln583Glu)
c.2752C>G (p.Gln918Glu)
c.2932C>G (p.Gln978Glu)
20g.51784369G>TCA409005765SALL4c.3058C>A (p.Gln1020Lys)
c.727C>A (p.Gln243Lys)
c.1747C>A (p.Gln583Lys)
c.2752C>A (p.Gln918Lys)
c.2932C>A (p.Gln978Lys)
20g.51784371delCA2580618158SALL4c.3058del (p.Gln1020SerfsTer?)
c.727del (p.Gln243SerfsTer?)
c.1747del (p.Gln583SerfsTer?)
c.2752del (p.Gln918SerfsTer?)
c.2932del (p.Gln978SerfsTer?)
ClinVar
20g.51784370G>ACA511025660SALL4c.3057C>T (p.Ser1019=)
c.726C>T (p.Ser242=)
c.1746C>T (p.Ser582=)
c.2751C>T (p.Ser917=)
c.2931C>T (p.Ser977=)
20g.51784370G>CCA9911934SALL4c.3057C>G (p.Ser1019=)
c.726C>G (p.Ser242=)
c.1746C>G (p.Ser582=)
c.2751C>G (p.Ser917=)
c.2931C>G (p.Ser977=)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784370G=CA2369155242SALL4c.3057C= (p.Ser1019=)
c.726C= (p.Ser242=)
c.1746C= (p.Ser582=)
c.2751C= (p.Ser917=)
c.2931C= (p.Ser977=)
20g.51784370G>TCA511025661SALL4c.3057C>A (p.Ser1019=)
c.726C>A (p.Ser242=)
c.1746C>A (p.Ser582=)
c.2751C>A (p.Ser917=)
c.2931C>A (p.Ser977=)
20g.51784371G>ACA409005767SALL4c.3056C>T (p.Ser1019Phe)
c.725C>T (p.Ser242Phe)
c.1745C>T (p.Ser582Phe)
c.2750C>T (p.Ser917Phe)
c.2930C>T (p.Ser977Phe)
20g.51784371G>CCA409005768SALL4c.3056C>G (p.Ser1019Cys)
c.725C>G (p.Ser242Cys)
c.1745C>G (p.Ser582Cys)
c.2750C>G (p.Ser917Cys)
c.2930C>G (p.Ser977Cys)
COSMIC
20g.51784371G>TCA409005769SALL4c.3056C>A (p.Ser1019Tyr)
c.725C>A (p.Ser242Tyr)
c.1745C>A (p.Ser582Tyr)
c.2750C>A (p.Ser917Tyr)
c.2930C>A (p.Ser977Tyr)
20g.51784372A=CA2369155243SALL4c.3055T= (p.Ser1019=)
c.724T= (p.Ser242=)
c.1744T= (p.Ser582=)
c.2749T= (p.Ser917=)
c.2929T= (p.Ser977=)
20g.51784372A>CCA409005770SALL4c.3055T>G (p.Ser1019Ala)
c.724T>G (p.Ser242Ala)
c.1744T>G (p.Ser582Ala)
c.2749T>G (p.Ser917Ala)
c.2929T>G (p.Ser977Ala)
20g.51784372A>GCA409005771SALL4c.3055T>C (p.Ser1019Pro)
c.724T>C (p.Ser242Pro)
c.1744T>C (p.Ser582Pro)
c.2749T>C (p.Ser917Pro)
c.2929T>C (p.Ser977Pro)
dbSNP gnomAD v3 gnomAD v4
20g.51784372A>TCA409005772SALL4c.3055T>A (p.Ser1019Thr)
c.724T>A (p.Ser242Thr)
c.1744T>A (p.Ser582Thr)
c.2749T>A (p.Ser917Thr)
c.2929T>A (p.Ser977Thr)
20g.51784373G>ACA511025667SALL4c.3054C>T (p.Gly1018=)
c.723C>T (p.Gly241=)
c.1743C>T (p.Gly581=)
c.2748C>T (p.Gly916=)
c.2928C>T (p.Gly976=)
COSMIC
20g.51784373G>CCA511025666SALL4c.3054C>G (p.Gly1018=)
c.723C>G (p.Gly241=)
c.1743C>G (p.Gly581=)
c.2748C>G (p.Gly916=)
c.2928C>G (p.Gly976=)
20g.51784373G>TCA511025663SALL4c.3054C>A (p.Gly1018=)
c.723C>A (p.Gly241=)
c.1743C>A (p.Gly581=)
c.2748C>A (p.Gly916=)
c.2928C>A (p.Gly976=)
20g.51784374C>ACA409005773SALL4c.3053G>T (p.Gly1018Val)
c.722G>T (p.Gly241Val)
c.1742G>T (p.Gly581Val)
c.2747G>T (p.Gly916Val)
c.2927G>T (p.Gly976Val)
20g.51784374C=CA2369155244SALL4c.3053G= (p.Gly1018=)
c.722G= (p.Gly241=)
c.1742G= (p.Gly581=)
c.2747G= (p.Gly916=)
c.2927G= (p.Gly976=)
20g.51784374C>GCA409005774SALL4c.3053G>C (p.Gly1018Ala)
c.722G>C (p.Gly241Ala)
c.1742G>C (p.Gly581Ala)
c.2747G>C (p.Gly916Ala)
c.2927G>C (p.Gly976Ala)
20g.51784374C>TCA409005775SALL4c.3053G>A (p.Gly1018Asp)
c.722G>A (p.Gly241Asp)
c.1742G>A (p.Gly581Asp)
c.2747G>A (p.Gly916Asp)
c.2927G>A (p.Gly976Asp)
dbSNP gnomAD v4
20g.51784375C>ACA409005776SALL4c.3052G>T (p.Gly1018Cys)
c.721G>T (p.Gly241Cys)
c.1741G>T (p.Gly581Cys)
c.2746G>T (p.Gly916Cys)
c.2926G>T (p.Gly976Cys)
COSMIC
20g.51784375C>GCA409005777SALL4c.3052G>C (p.Gly1018Arg)
c.721G>C (p.Gly241Arg)
c.1741G>C (p.Gly581Arg)
c.2746G>C (p.Gly916Arg)
c.2926G>C (p.Gly976Arg)
20g.51784375C>TCA409005778SALL4c.3052G>A (p.Gly1018Ser)
c.721G>A (p.Gly241Ser)
c.1741G>A (p.Gly581Ser)
c.2746G>A (p.Gly916Ser)
c.2926G>A (p.Gly976Ser)
gnomAD v4
20g.51784376A>CCA409005780SALL4c.3051T>G (p.Asp1017Glu)
c.720T>G (p.Asp240Glu)
c.1740T>G (p.Asp580Glu)
c.2745T>G (p.Asp915Glu)
c.2925T>G (p.Asp975Glu)
20g.51784376A>GCA511025668SALL4c.3051T>C (p.Asp1017=)
c.720T>C (p.Asp240=)
c.1740T>C (p.Asp580=)
c.2745T>C (p.Asp915=)
c.2925T>C (p.Asp975=)
COSMIC
20g.51784376A>TCA409005779SALL4c.3051T>A (p.Asp1017Glu)
c.720T>A (p.Asp240Glu)
c.1740T>A (p.Asp580Glu)
c.2745T>A (p.Asp915Glu)
c.2925T>A (p.Asp975Glu)
20g.51784377T>ACA9911935SALL4c.3050A>T (p.Asp1017Val)
c.719A>T (p.Asp240Val)
c.1739A>T (p.Asp580Val)
c.2744A>T (p.Asp915Val)
c.2924A>T (p.Asp975Val)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784377T>CCA409005781SALL4c.3050A>G (p.Asp1017Gly)
c.719A>G (p.Asp240Gly)
c.1739A>G (p.Asp580Gly)
c.2744A>G (p.Asp915Gly)
c.2924A>G (p.Asp975Gly)
20g.51784377T>GCA409005782SALL4c.3050A>C (p.Asp1017Ala)
c.719A>C (p.Asp240Ala)
c.1739A>C (p.Asp580Ala)
c.2744A>C (p.Asp915Ala)
c.2924A>C (p.Asp975Ala)
20g.51784377T=CA2369155245SALL4c.3050A= (p.Asp1017=)
c.719A= (p.Asp240=)
c.1739A= (p.Asp580=)
c.2744A= (p.Asp915=)
c.2924A= (p.Asp975=)
20g.51784378C>ACA409005783SALL4c.3049G>T (p.Asp1017Tyr)
c.718G>T (p.Asp240Tyr)
c.1738G>T (p.Asp580Tyr)
c.2743G>T (p.Asp915Tyr)
c.2923G>T (p.Asp975Tyr)
20g.51784378C>GCA409005784SALL4c.3049G>C (p.Asp1017His)
c.718G>C (p.Asp240His)
c.1738G>C (p.Asp580His)
c.2743G>C (p.Asp915His)
c.2923G>C (p.Asp975His)
20g.51784378C>TCA409005785SALL4c.3049G>A (p.Asp1017Asn)
c.718G>A (p.Asp240Asn)
c.1738G>A (p.Asp580Asn)
c.2743G>A (p.Asp915Asn)
c.2923G>A (p.Asp975Asn)
20g.51784379C>ACA409005786SALL4c.3048G>T (p.Met1016Ile)
c.717G>T (p.Met239Ile)
c.1737G>T (p.Met579Ile)
c.2742G>T (p.Met914Ile)
c.2922G>T (p.Met974Ile)
20g.51784379C>GCA409005787SALL4c.3048G>C (p.Met1016Ile)
c.717G>C (p.Met239Ile)
c.1737G>C (p.Met579Ile)
c.2742G>C (p.Met914Ile)
c.2922G>C (p.Met974Ile)
20g.51784379C>TCA409005788SALL4c.3048G>A (p.Met1016Ile)
c.717G>A (p.Met239Ile)
c.1737G>A (p.Met579Ile)
c.2742G>A (p.Met914Ile)
c.2922G>A (p.Met974Ile)
20g.51784380A=CA2369155246SALL4c.3047T= (p.Met1016=)
c.716T= (p.Met239=)
c.1736T= (p.Met579=)
c.2741T= (p.Met914=)
c.2921T= (p.Met974=)
20g.51784380A>CCA409005789SALL4c.3047T>G (p.Met1016Arg)
c.716T>G (p.Met239Arg)
c.1736T>G (p.Met579Arg)
c.2741T>G (p.Met914Arg)
c.2921T>G (p.Met974Arg)
20g.51784380A>GCA409005790SALL4c.3047T>C (p.Met1016Thr)
c.716T>C (p.Met239Thr)
c.1736T>C (p.Met579Thr)
c.2741T>C (p.Met914Thr)
c.2921T>C (p.Met974Thr)
dbSNP gnomAD v3 gnomAD v4
20g.51784380A>TCA409005791SALL4c.3047T>A (p.Met1016Lys)
c.716T>A (p.Met239Lys)
c.1736T>A (p.Met579Lys)
c.2741T>A (p.Met914Lys)
c.2921T>A (p.Met974Lys)
dbSNP gnomAD v2 gnomAD v4
20g.51784381T>ACA409005794SALL4c.3046A>T (p.Met1016Leu)
c.715A>T (p.Met239Leu)
c.1735A>T (p.Met579Leu)
c.2740A>T (p.Met914Leu)
c.2920A>T (p.Met974Leu)
20g.51784381T>CCA409005793SALL4c.3046A>G (p.Met1016Val)
c.715A>G (p.Met239Val)
c.1735A>G (p.Met579Val)
c.2740A>G (p.Met914Val)
c.2920A>G (p.Met974Val)
20g.51784381T>GCA409005792SALL4c.3046A>C (p.Met1016Leu)
c.715A>C (p.Met239Leu)
c.1735A>C (p.Met579Leu)
c.2740A>C (p.Met914Leu)
c.2920A>C (p.Met974Leu)
20g.51784382C>ACA409005795SALL4c.3045G>T (p.Lys1015Asn)
c.714G>T (p.Lys238Asn)
c.1734G>T (p.Lys578Asn)
c.2739G>T (p.Lys913Asn)
c.2919G>T (p.Lys973Asn)
20g.51784382C=CA2369155247SALL4c.3045G= (p.Lys1015=)
c.714G= (p.Lys238=)
c.1734G= (p.Lys578=)
c.2739G= (p.Lys913=)
c.2919G= (p.Lys973=)
20g.51784382C>GCA409005796SALL4c.3045G>C (p.Lys1015Asn)
c.714G>C (p.Lys238Asn)
c.1734G>C (p.Lys578Asn)
c.2739G>C (p.Lys913Asn)
c.2919G>C (p.Lys973Asn)
20g.51784382C>TCA9911936SALL4c.3045G>A (p.Lys1015=)
c.714G>A (p.Lys238=)
c.1734G>A (p.Lys578=)
c.2739G>A (p.Lys913=)
c.2919G>A (p.Lys973=)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784383T>ACA409005797SALL4c.3044A>T (p.Lys1015Met)
c.713A>T (p.Lys238Met)
c.1733A>T (p.Lys578Met)
c.2738A>T (p.Lys913Met)
c.2918A>T (p.Lys973Met)
20g.51784383T>CCA409005798SALL4c.3044A>G (p.Lys1015Arg)
c.713A>G (p.Lys238Arg)
c.1733A>G (p.Lys578Arg)
c.2738A>G (p.Lys913Arg)
c.2918A>G (p.Lys973Arg)
gnomAD v4
20g.51784383T>GCA409005799SALL4c.3044A>C (p.Lys1015Thr)
c.713A>C (p.Lys238Thr)
c.1733A>C (p.Lys578Thr)
c.2738A>C (p.Lys913Thr)
c.2918A>C (p.Lys973Thr)
20g.51784384T>ACA409005800SALL4c.3043A>T (p.Lys1015Ter)
c.712A>T (p.Lys238Ter)
c.1732A>T (p.Lys578Ter)
c.2737A>T (p.Lys913Ter)
c.2917A>T (p.Lys973Ter)
20g.51784384T>CCA9911938SALL4c.3043A>G (p.Lys1015Glu)
c.712A>G (p.Lys238Glu)
c.1732A>G (p.Lys578Glu)
c.2737A>G (p.Lys913Glu)
c.2917A>G (p.Lys973Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784384T>GCA9911937SALL4c.3043A>C (p.Lys1015Gln)
c.712A>C (p.Lys238Gln)
c.1732A>C (p.Lys578Gln)
c.2737A>C (p.Lys913Gln)
c.2917A>C (p.Lys973Gln)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.51784384T=CA2369155248SALL4c.3043A= (p.Lys1015=)
c.712A= (p.Lys238=)
c.1732A= (p.Lys578=)
c.2737A= (p.Lys913=)
c.2917A= (p.Lys973=)
20g.51784385G>ACA511025679SALL4c.3042C>T (p.Ser1014=)
c.711C>T (p.Ser237=)
c.1731C>T (p.Ser577=)
c.2736C>T (p.Ser912=)
c.2916C>T (p.Ser972=)
gnomAD v4
20g.51784385G>CCA511025680SALL4c.3042C>G (p.Ser1014=)
c.711C>G (p.Ser237=)
c.1731C>G (p.Ser577=)
c.2736C>G (p.Ser912=)
c.2916C>G (p.Ser972=)
20g.51784385G>TCA511025681SALL4c.3042C>A (p.Ser1014=)
c.711C>A (p.Ser237=)
c.1731C>A (p.Ser577=)
c.2736C>A (p.Ser912=)
c.2916C>A (p.Ser972=)
20g.51784386G>ACA409005803SALL4c.3041C>T (p.Ser1014Phe)
c.710C>T (p.Ser237Phe)
c.1730C>T (p.Ser577Phe)
c.2735C>T (p.Ser912Phe)
c.2915C>T (p.Ser972Phe)
dbSNP gnomAD v4
20g.51784386G>CCA409005802SALL4c.3041C>G (p.Ser1014Cys)
c.710C>G (p.Ser237Cys)
c.1730C>G (p.Ser577Cys)
c.2735C>G (p.Ser912Cys)
c.2915C>G (p.Ser972Cys)
20g.51784386G=CA2369155249SALL4c.3041C= (p.Ser1014=)
c.710C= (p.Ser237=)
c.1730C= (p.Ser577=)
c.2735C= (p.Ser912=)
c.2915C= (p.Ser972=)
20g.51784386G>TCA409005801SALL4c.3041C>A (p.Ser1014Tyr)
c.710C>A (p.Ser237Tyr)
c.1730C>A (p.Ser577Tyr)
c.2735C>A (p.Ser912Tyr)
c.2915C>A (p.Ser972Tyr)
20g.51784387A=CA2369155250SALL4c.3040T= (p.Ser1014=)
c.709T= (p.Ser237=)
c.1729T= (p.Ser577=)
c.2734T= (p.Ser912=)
c.2914T= (p.Ser972=)
20g.51784387A>CCA409005804SALL4c.3040T>G (p.Ser1014Ala)
c.709T>G (p.Ser237Ala)
c.1729T>G (p.Ser577Ala)
c.2734T>G (p.Ser912Ala)
c.2914T>G (p.Ser972Ala)
dbSNP gnomAD v4
20g.51784387A>GCA409005805SALL4c.3040T>C (p.Ser1014Pro)
c.709T>C (p.Ser237Pro)
c.1729T>C (p.Ser577Pro)
c.2734T>C (p.Ser912Pro)
c.2914T>C (p.Ser972Pro)
20g.51784387A>TCA409005806SALL4c.3040T>A (p.Ser1014Thr)
c.709T>A (p.Ser237Thr)
c.1729T>A (p.Ser577Thr)
c.2734T>A (p.Ser912Thr)
c.2914T>A (p.Ser972Thr)
20g.51784388G>ACA511025683SALL4c.3039C>T (p.Val1013=)
c.708C>T (p.Val236=)
c.1728C>T (p.Val576=)
c.2733C>T (p.Val911=)
c.2913C>T (p.Val971=)
dbSNP gnomAD v2
20g.51784388G>CCA315365859SALL4c.3039C>G (p.Val1013=)
c.708C>G (p.Val236=)
c.1728C>G (p.Val576=)
c.2733C>G (p.Val911=)
c.2913C>G (p.Val971=)
dbSNP gnomAD v4
20g.51784388G=CA2369155251SALL4c.3039C= (p.Val1013=)
c.708C= (p.Val236=)
c.1728C= (p.Val576=)
c.2733C= (p.Val911=)
c.2913C= (p.Val971=)
20g.51784388G>TCA511025684SALL4c.3039C>A (p.Val1013=)
c.708C>A (p.Val236=)
c.1728C>A (p.Val576=)
c.2733C>A (p.Val911=)
c.2913C>A (p.Val971=)

Number of alleles fetched