Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.51139368C>ACA395883529SALL1c.2854G>T (p.Val952Phe)
c.2563G>T (p.Val855Phe)
c.77-1816G>T (n.77-1816G>T)
 dbSNP gnomAD v3 gnomAD v4
16g.51139368C=CA2222017838SALL1c.2854G= (p.Val952=)
c.2563G= (p.Val855=)
c.77-1816G= (n.77-1816G=)
16g.51139368C>GCA395883530SALL1c.2854G>C (p.Val952Leu)
c.2563G>C (p.Val855Leu)
c.77-1816G>C (n.77-1816G>C)
16g.51139368C>TCA8053027SALL1c.2854G>A (p.Val952Ile)
c.2563G>A (p.Val855Ile)
c.77-1816G>A (n.77-1816G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51139369C>ACA495780093SALL1c.2853G>T (p.Ala951=)
c.2562G>T (p.Ala854=)
c.77-1817G>T (n.77-1817G>T)
16g.51139369C=CA2222017842SALL1c.2853G= (p.Ala951=)
c.2562G= (p.Ala854=)
c.77-1817G= (n.77-1817G=)
16g.51139369C>GCA495780094SALL1c.2853G>C (p.Ala951=)
c.2562G>C (p.Ala854=)
c.77-1817G>C (n.77-1817G>C)
 gnomAD v4 COSMIC
16g.51139369C>TCA8053028SALL1c.2853G>A (p.Ala951=)
c.2562G>A (p.Ala854=)
c.77-1817G>A (n.77-1817G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.51139369_51139370insCCTCA2807012906SALL1c.2852_2853insAGG (p.Ala951_Val952insGly)
c.2561_2562insAGG (p.Ala854_Val855insGly)
c.77-1818_77-1817insAGG (n.77-1818_77-1817insAGG)
16g.51139370G>ACA8053029SALL1c.2852C>T (p.Ala951Val)
c.2561C>T (p.Ala854Val)
c.77-1818C>T (n.77-1818C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51139370G>CCA395883535SALL1c.2852C>G (p.Ala951Gly)
c.2561C>G (p.Ala854Gly)
c.77-1818C>G (n.77-1818C>G)
 dbSNP gnomAD v2 gnomAD v4
16g.51139370G=CA2222017849SALL1c.2852C= (p.Ala951=)
c.2561C= (p.Ala854=)
c.77-1818C= (n.77-1818C=)
16g.51139370G>TCA395883538SALL1c.2852C>A (p.Ala951Glu)
c.2561C>A (p.Ala854Glu)
c.77-1818C>A (n.77-1818C>A)
 dbSNP gnomAD v3 gnomAD v4
16g.51139370dupCA2567641251SALL1c.2852dup (p.Val952GlyfsTer24)
c.2561dup (p.Val855GlyfsTer24)
c.77-1818dup (n.77-1818dup)
16g.51139371C>ACA395883541SALL1c.2851G>T (p.Ala951Ser)
c.2560G>T (p.Ala854Ser)
c.77-1819G>T (n.77-1819G>T)
 dbSNP gnomAD v4
16g.51139371C=CA2222017852SALL1c.2851G= (p.Ala951=)
c.2560G= (p.Ala854=)
c.77-1819G= (n.77-1819G=)
16g.51139371C>GCA395883543SALL1c.2851G>C (p.Ala951Pro)
c.2560G>C (p.Ala854Pro)
c.77-1819G>C (n.77-1819G>C)
16g.51139371C>TCA395883545SALL1c.2851G>A (p.Ala951Thr)
c.2560G>A (p.Ala854Thr)
c.77-1819G>A (n.77-1819G>A)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
16g.51139372T>ACA395883547SALL1c.2850A>T (p.Arg950Ser)
c.2559A>T (p.Arg853Ser)
c.77-1820A>T (n.77-1820A>T)
16g.51139372T>CCA495780095SALL1c.2850A>G (p.Arg950=)
c.2559A>G (p.Arg853=)
c.77-1820A>G (n.77-1820A>G)
16g.51139372T>GCA395883549SALL1c.2850A>C (p.Arg950Ser)
c.2559A>C (p.Arg853Ser)
c.77-1820A>C (n.77-1820A>C)
16g.51139373C>ACA395883550SALL1c.2849G>T (p.Arg950Ile)
c.2558G>T (p.Arg853Ile)
c.77-1821G>T (n.77-1821G>T)
16g.51139373C=CA2222017855SALL1c.2849G= (p.Arg950=)
c.2558G= (p.Arg853=)
c.77-1821G= (n.77-1821G=)
16g.51139373C>GCA8053030SALL1c.2849G>C (p.Arg950Thr)
c.2558G>C (p.Arg853Thr)
c.77-1821G>C (n.77-1821G>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51139373C>TCA395883552SALL1c.2849G>A (p.Arg950Lys)
c.2558G>A (p.Arg853Lys)
c.77-1821G>A (n.77-1821G>A)
 COSMIC
16g.51139374T>ACA395883554SALL1c.2848A>T (p.Arg950Ter)
c.2557A>T (p.Arg853Ter)
c.77-1822A>T (n.77-1822A>T)
16g.51139374T>CCA395883555SALL1c.2848A>G (p.Arg950Gly)
c.2557A>G (p.Arg853Gly)
c.77-1822A>G (n.77-1822A>G)
16g.51139374T>GCA495780096SALL1c.2848A>C (p.Arg950=)
c.2557A>C (p.Arg853=)
c.77-1822A>C (n.77-1822A>C)
16g.51139374_51139375insTACA2807012907SALL1c.2847_2848insTA (p.Arg950Ter)
c.2556_2557insTA (p.Arg853Ter)
c.77-1823_77-1822insTA (n.77-1823_77-1822insTA)
16g.51139375C>ACA395883557SALL1c.2847G>T (p.Gln949His)
c.2556G>T (p.Gln852His)
c.77-1823G>T (n.77-1823G>T)
 COSMIC
16g.51139375C>GCA395883558SALL1c.2847G>C (p.Gln949His)
c.2556G>C (p.Gln852His)
c.77-1823G>C (n.77-1823G>C)
16g.51139375C>TCA495780097SALL1c.2847G>A (p.Gln949=)
c.2556G>A (p.Gln852=)
c.77-1823G>A (n.77-1823G>A)
 gnomAD v4
16g.51139376T>ACA395883562SALL1c.2846A>T (p.Gln949Leu)
c.2555A>T (p.Gln852Leu)
c.77-1824A>T (n.77-1824A>T)
 dbSNP
16g.51139376T>CCA281301056SALL1c.2846A>G (p.Gln949Arg)
c.2555A>G (p.Gln852Arg)
c.77-1824A>G (n.77-1824A>G)
 ClinVar dbSNP gnomAD v4
16g.51139376T>GCA395883564SALL1c.2846A>C (p.Gln949Pro)
c.2555A>C (p.Gln852Pro)
c.77-1824A>C (n.77-1824A>C)
16g.51139376T=CA2222017857SALL1c.2846A= (p.Gln949=)
c.2555A= (p.Gln852=)
c.77-1824A= (n.77-1824A=)
16g.51139378_51139379delCA2807012908SALL1c.2845_2846del (p.Gln949GlufsTer26)
c.2554_2555del (p.Gln852GlufsTer26)
c.77-1825_77-1824del (n.77-1825_77-1824del)
16g.51139377G>ACA395883568SALL1c.2845C>T (p.Gln949Ter)
c.2554C>T (p.Gln852Ter)
c.77-1825C>T (n.77-1825C>T)
16g.51139377G>CCA395883571SALL1c.2845C>G (p.Gln949Glu)
c.2554C>G (p.Gln852Glu)
c.77-1825C>G (n.77-1825C>G)
16g.51139377G>TCA395883573SALL1c.2845C>A (p.Gln949Lys)
c.2554C>A (p.Gln852Lys)
c.77-1825C>A (n.77-1825C>A)
 COSMIC
16g.51139378T>ACA495780103SALL1c.2844A>T (p.Pro948=)
c.2553A>T (p.Pro851=)
c.77-1826A>T (n.77-1826A>T)
16g.51139378T>CCA495780101SALL1c.2844A>G (p.Pro948=)
c.2553A>G (p.Pro851=)
c.77-1826A>G (n.77-1826A>G)
16g.51139378T>GCA495780099SALL1c.2844A>C (p.Pro948=)
c.2553A>C (p.Pro851=)
c.77-1826A>C (n.77-1826A>C)
16g.51139379G>ACA395883575SALL1c.2843C>T (p.Pro948Leu)
c.2552C>T (p.Pro851Leu)
c.77-1827C>T (n.77-1827C>T)
 gnomAD v4
16g.51139379G>CCA395883577SALL1c.2843C>G (p.Pro948Arg)
c.2552C>G (p.Pro851Arg)
c.77-1827C>G (n.77-1827C>G)
 gnomAD v4
16g.51139379G>TCA395883579SALL1c.2843C>A (p.Pro948Gln)
c.2552C>A (p.Pro851Gln)
c.77-1827C>A (n.77-1827C>A)
16g.51139380G>ACA395883581SALL1c.2842C>T (p.Pro948Ser)
c.2551C>T (p.Pro851Ser)
c.77-1828C>T (n.77-1828C>T)
16g.51139380G>CCA395883583SALL1c.2842C>G (p.Pro948Ala)
c.2551C>G (p.Pro851Ala)
c.77-1828C>G (n.77-1828C>G)
 dbSNP gnomAD v2 gnomAD v4
16g.51139380G=CA2222017859SALL1c.2842C= (p.Pro948=)
c.2551C= (p.Pro851=)
c.77-1828C= (n.77-1828C=)
16g.51139380G>TCA395883585SALL1c.2842C>A (p.Pro948Thr)
c.2551C>A (p.Pro851Thr)
c.77-1828C>A (n.77-1828C>A)
 dbSNP gnomAD v3 gnomAD v4
16g.51139381T>ACA395883587SALL1c.2841A>T (p.Lys947Asn)
c.2550A>T (p.Lys850Asn)
c.77-1829A>T (n.77-1829A>T)
16g.51139381T>CCA495780105SALL1c.2841A>G (p.Lys947=)
c.2550A>G (p.Lys850=)
c.77-1829A>G (n.77-1829A>G)
 dbSNP gnomAD v3 gnomAD v4
16g.51139381T>GCA395883588SALL1c.2841A>C (p.Lys947Asn)
c.2550A>C (p.Lys850Asn)
c.77-1829A>C (n.77-1829A>C)
16g.51139381T=CA2222017864SALL1c.2841A= (p.Lys947=)
c.2550A= (p.Lys850=)
c.77-1829A= (n.77-1829A=)
16g.51139382T>ACA395883592SALL1c.2840A>T (p.Lys947Ile)
c.2549A>T (p.Lys850Ile)
c.77-1830A>T (n.77-1830A>T)
16g.51139382T>CCA395883589SALL1c.2840A>G (p.Lys947Arg)
c.2549A>G (p.Lys850Arg)
c.77-1830A>G (n.77-1830A>G)
16g.51139382T>GCA395883591SALL1c.2840A>C (p.Lys947Thr)
c.2549A>C (p.Lys850Thr)
c.77-1830A>C (n.77-1830A>C)
16g.51139383T>ACA395883594SALL1c.2839A>T (p.Lys947Ter)
c.2548A>T (p.Lys850Ter)
c.77-1831A>T (n.77-1831A>T)
16g.51139383T>CCA395883596SALL1c.2839A>G (p.Lys947Glu)
c.2548A>G (p.Lys850Glu)
c.77-1831A>G (n.77-1831A>G)
16g.51139383T>GCA395883597SALL1c.2839A>C (p.Lys947Gln)
c.2548A>C (p.Lys850Gln)
c.77-1831A>C (n.77-1831A>C)
16g.51139384C>ACA395883598SALL1c.2838G>T (p.Glu946Asp)
c.2547G>T (p.Glu849Asp)
c.77-1832G>T (n.77-1832G>T)
16g.51139384C>GCA395883599SALL1c.2838G>C (p.Glu946Asp)
c.2547G>C (p.Glu849Asp)
c.77-1832G>C (n.77-1832G>C)
16g.51139384C>TCA495780109SALL1c.2838G>A (p.Glu946=)
c.2547G>A (p.Glu849=)
c.77-1832G>A (n.77-1832G>A)
 COSMIC
16g.51139385T>ACA395883601SALL1c.2837A>T (p.Glu946Val)
c.2546A>T (p.Glu849Val)
c.77-1833A>T (n.77-1833A>T)
16g.51139385T>CCA395883602SALL1c.2837A>G (p.Glu946Gly)
c.2546A>G (p.Glu849Gly)
c.77-1833A>G (n.77-1833A>G)
 dbSNP gnomAD v4 COSMIC
16g.51139385T>GCA395883604SALL1c.2837A>C (p.Glu946Ala)
c.2546A>C (p.Glu849Ala)
c.77-1833A>C (n.77-1833A>C)
16g.51139385T=CA2222017867SALL1c.2837A= (p.Glu946=)
c.2546A= (p.Glu849=)
c.77-1833A= (n.77-1833A=)
16g.51139386C>ACA395883606SALL1c.2836G>T (p.Glu946Ter)
c.2545G>T (p.Glu849Ter)
c.77-1834G>T (n.77-1834G>T)
16g.51139386C=CA2222017873SALL1c.2836G= (p.Glu946=)
c.2545G= (p.Glu849=)
c.77-1834G= (n.77-1834G=)
16g.51139386C>GCA395883608SALL1c.2836G>C (p.Glu946Gln)
c.2545G>C (p.Glu849Gln)
c.77-1834G>C (n.77-1834G>C)
16g.51139386C>TCA8053031SALL1c.2836G>A (p.Glu946Lys)
c.2545G>A (p.Glu849Lys)
c.77-1834G>A (n.77-1834G>A)
 dbSNP ExAC gnomAD v2
16g.51139387C>ACA395883614SALL1c.2835G>T (p.Glu945Asp)
c.2544G>T (p.Glu848Asp)
c.77-1835G>T (n.77-1835G>T)
16g.51139387C>GCA395883612SALL1c.2835G>C (p.Glu945Asp)
c.2544G>C (p.Glu848Asp)
c.77-1835G>C (n.77-1835G>C)
16g.51139387C>TCA495780111SALL1c.2835G>A (p.Glu945=)
c.2544G>A (p.Glu848=)
c.77-1835G>A (n.77-1835G>A)
 COSMIC
16g.51139388T>ACA395883616SALL1c.2834A>T (p.Glu945Val)
c.2543A>T (p.Glu848Val)
c.77-1836A>T (n.77-1836A>T)
16g.51139388T>CCA395883620SALL1c.2834A>G (p.Glu945Gly)
c.2543A>G (p.Glu848Gly)
c.77-1836A>G (n.77-1836A>G)
 gnomAD v4
16g.51139388T>GCA395883618SALL1c.2834A>C (p.Glu945Ala)
c.2543A>C (p.Glu848Ala)
c.77-1836A>C (n.77-1836A>C)
16g.51139389C>ACA395883622SALL1c.2833G>T (p.Glu945Ter)
c.2542G>T (p.Glu848Ter)
c.77-1837G>T (n.77-1837G>T)
16g.51139389C>GCA395883624SALL1c.2833G>C (p.Glu945Gln)
c.2542G>C (p.Glu848Gln)
c.77-1837G>C (n.77-1837G>C)
16g.51139389C>TCA395883626SALL1c.2833G>A (p.Glu945Lys)
c.2542G>A (p.Glu848Lys)
c.77-1837G>A (n.77-1837G>A)
16g.51139390A=CA2222017876SALL1c.2832T= (p.Ile944=)
c.2541T= (p.Ile847=)
c.77-1838T= (n.77-1838T=)
16g.51139390A>CCA395883627SALL1c.2832T>G (p.Ile944Met)
c.2541T>G (p.Ile847Met)
c.77-1838T>G (n.77-1838T>G)
16g.51139390A>GCA495780117SALL1c.2832T>C (p.Ile944=)
c.2541T>C (p.Ile847=)
c.77-1838T>C (n.77-1838T>C)
 dbSNP gnomAD v4
16g.51139390A>TCA495780118SALL1c.2832T>A (p.Ile944=)
c.2541T>A (p.Ile847=)
c.77-1838T>A (n.77-1838T>A)
16g.51139391A=CA2222017879SALL1c.2831T= (p.Ile944=)
c.2540T= (p.Ile847=)
c.77-1839T= (n.77-1839T=)
16g.51139391A>CCA395883629SALL1c.2831T>G (p.Ile944Ser)
c.2540T>G (p.Ile847Ser)
c.77-1839T>G (n.77-1839T>G)
16g.51139391A>GCA8053032SALL1c.2831T>C (p.Ile944Thr)
c.2540T>C (p.Ile847Thr)
c.77-1839T>C (n.77-1839T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51139391A>TCA395883631SALL1c.2831T>A (p.Ile944Asn)
c.2540T>A (p.Ile847Asn)
c.77-1839T>A (n.77-1839T>A)
16g.51139392T>ACA395883634SALL1c.2830A>T (p.Ile944Phe)
c.2539A>T (p.Ile847Phe)
c.77-1840A>T (n.77-1840A>T)
16g.51139392T>CCA395883636SALL1c.2830A>G (p.Ile944Val)
c.2539A>G (p.Ile847Val)
c.77-1840A>G (n.77-1840A>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.51139392T>GCA395883638SALL1c.2830A>C (p.Ile944Leu)
c.2539A>C (p.Ile847Leu)
c.77-1840A>C (n.77-1840A>C)
 dbSNP gnomAD v3 gnomAD v4
16g.51139392T=CA2222017883SALL1c.2830A= (p.Ile944=)
c.2539A= (p.Ile847=)
c.77-1840A= (n.77-1840A=)
16g.51139393G>ACA495780120SALL1c.2829C>T (p.Ser943=)
c.2538C>T (p.Ser846=)
c.77-1841C>T (n.77-1841C>T)
16g.51139393G>CCA395883640SALL1c.2829C>G (p.Ser943Arg)
c.2538C>G (p.Ser846Arg)
c.77-1841C>G (n.77-1841C>G)
 gnomAD v4
16g.51139393G>TCA395883641SALL1c.2829C>A (p.Ser943Arg)
c.2538C>A (p.Ser846Arg)
c.77-1841C>A (n.77-1841C>A)
16g.51139394C>ACA395883644SALL1c.2828G>T (p.Ser943Ile)
c.2537G>T (p.Ser846Ile)
c.77-1842G>T (n.77-1842G>T)
16g.51139394C>GCA395883647SALL1c.2828G>C (p.Ser943Thr)
c.2537G>C (p.Ser846Thr)
c.77-1842G>C (n.77-1842G>C)
16g.51139394C>TCA395883645SALL1c.2828G>A (p.Ser943Asn)
c.2537G>A (p.Ser846Asn)
c.77-1842G>A (n.77-1842G>A)
16g.51139395T>ACA395883649SALL1c.2827A>T (p.Ser943Cys)
c.2536A>T (p.Ser846Cys)
c.77-1843A>T (n.77-1843A>T)
16g.51139395T>CCA281301058SALL1c.2827A>G (p.Ser943Gly)
c.2536A>G (p.Ser846Gly)
c.77-1843A>G (n.77-1843A>G)
 dbSNP
16g.51139395T>GCA395883652SALL1c.2827A>C (p.Ser943Arg)
c.2536A>C (p.Ser846Arg)
c.77-1843A>C (n.77-1843A>C)
16g.51139395T=CA2222017888SALL1c.2827A= (p.Ser943=)
c.2536A= (p.Ser846=)
c.77-1843A= (n.77-1843A=)
16g.51139396G>ACA495780122SALL1c.2826C>T (p.Pro942=)
c.2535C>T (p.Pro845=)
c.77-1844C>T (n.77-1844C>T)
 dbSNP gnomAD v4
16g.51139396G>CCA495780124SALL1c.2826C>G (p.Pro942=)
c.2535C>G (p.Pro845=)
c.77-1844C>G (n.77-1844C>G)
16g.51139396G=CA2222017892SALL1c.2826C= (p.Pro942=)
c.2535C= (p.Pro845=)
c.77-1844C= (n.77-1844C=)
16g.51139396G>TCA495780125SALL1c.2826C>A (p.Pro942=)
c.2535C>A (p.Pro845=)
c.77-1844C>A (n.77-1844C>A)
16g.51139397G>ACA8053033SALL1c.2825C>T (p.Pro942Leu)
c.2534C>T (p.Pro845Leu)
c.77-1845C>T (n.77-1845C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51139397G>CCA395883656SALL1c.2825C>G (p.Pro942Arg)
c.2534C>G (p.Pro845Arg)
c.77-1845C>G (n.77-1845C>G)
16g.51139397G=CA2222017900SALL1c.2825C= (p.Pro942=)
c.2534C= (p.Pro845=)
c.77-1845C= (n.77-1845C=)
16g.51139397G>TCA10604890SALL1c.2825C>A (p.Pro942His)
c.2534C>A (p.Pro845His)
c.77-1845C>A (n.77-1845C>A)
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.51139398G>ACA395883660SALL1c.2824C>T (p.Pro942Ser)
c.2533C>T (p.Pro845Ser)
c.77-1846C>T (n.77-1846C>T)
 gnomAD v4
16g.51139398G>CCA395883662SALL1c.2824C>G (p.Pro942Ala)
c.2533C>G (p.Pro845Ala)
c.77-1846C>G (n.77-1846C>G)
16g.51139398G>TCA395883664SALL1c.2824C>A (p.Pro942Thr)
c.2533C>A (p.Pro845Thr)
c.77-1846C>A (n.77-1846C>A)
 gnomAD v4
16g.51139399T>ACA495780127SALL1c.2823A>T (p.Ser941=)
c.2532A>T (p.Ser844=)
c.77-1847A>T (n.77-1847A>T)
16g.51139399T>CCA495780130SALL1c.2823A>G (p.Ser941=)
c.2532A>G (p.Ser844=)
c.77-1847A>G (n.77-1847A>G)
16g.51139399T>GCA495780128SALL1c.2823A>C (p.Ser941=)
c.2532A>C (p.Ser844=)
c.77-1847A>C (n.77-1847A>C)
16g.51139400G>ACA395883668SALL1c.2822C>T (p.Ser941Leu)
c.2531C>T (p.Ser844Leu)
c.77-1848C>T (n.77-1848C>T)
16g.51139400G>CCA395883670SALL1c.2822C>G (p.Ser941Ter)
c.2531C>G (p.Ser844Ter)
c.77-1848C>G (n.77-1848C>G)
16g.51139400G>TCA395883666SALL1c.2822C>A (p.Ser941Ter)
c.2531C>A (p.Ser844Ter)
c.77-1848C>A (n.77-1848C>A)
16g.51139401A>CCA395883672SALL1c.2821T>G (p.Ser941Ala)
c.2530T>G (p.Ser844Ala)
c.77-1849T>G (n.77-1849T>G)
16g.51139401A>GCA395883674SALL1c.2821T>C (p.Ser941Pro)
c.2530T>C (p.Ser844Pro)
c.77-1849T>C (n.77-1849T>C)
 gnomAD v4
16g.51139401A>TCA395883676SALL1c.2821T>A (p.Ser941Thr)
c.2530T>A (p.Ser844Thr)
c.77-1849T>A (n.77-1849T>A)
16g.51139402C>ACA395883678SALL1c.2820G>T (p.Lys940Asn)
c.2529G>T (p.Lys843Asn)
c.77-1850G>T (n.77-1850G>T)
16g.51139402C>GCA395883680SALL1c.2820G>C (p.Lys940Asn)
c.2529G>C (p.Lys843Asn)
c.77-1850G>C (n.77-1850G>C)
16g.51139402C>TCA495780135SALL1c.2820G>A (p.Lys940=)
c.2529G>A (p.Lys843=)
c.77-1850G>A (n.77-1850G>A)
16g.51139403T>ACA395883683SALL1c.2819A>T (p.Lys940Met)
c.2528A>T (p.Lys843Met)
c.77-1851A>T (n.77-1851A>T)
16g.51139403T>CCA395883685SALL1c.2819A>G (p.Lys940Arg)
c.2528A>G (p.Lys843Arg)
c.77-1851A>G (n.77-1851A>G)
 gnomAD v4
16g.51139403T>GCA395883688SALL1c.2819A>C (p.Lys940Thr)
c.2528A>C (p.Lys843Thr)
c.77-1851A>C (n.77-1851A>C)
16g.51139404T>ACA395883690SALL1c.2818A>T (p.Lys940Ter)
c.2527A>T (p.Lys843Ter)
c.77-1852A>T (n.77-1852A>T)
16g.51139404T>CCA395883692SALL1c.2818A>G (p.Lys940Glu)
c.2527A>G (p.Lys843Glu)
c.77-1852A>G (n.77-1852A>G)
16g.51139404T>GCA395883694SALL1c.2818A>C (p.Lys940Gln)
c.2527A>C (p.Lys843Gln)
c.77-1852A>C (n.77-1852A>C)
16g.51139405G>ACA495780138SALL1c.2817C>T (p.His939=)
c.2526C>T (p.His842=)
c.77-1853C>T (n.77-1853C>T)
 dbSNP gnomAD v2 gnomAD v4
16g.51139405G>CCA395883695SALL1c.2817C>G (p.His939Gln)
c.2526C>G (p.His842Gln)
c.77-1853C>G (n.77-1853C>G)
16g.51139405G=CA2222017906SALL1c.2817C= (p.His939=)
c.2526C= (p.His842=)
c.77-1853C= (n.77-1853C=)
16g.51139405G>TCA395883698SALL1c.2817C>A (p.His939Gln)
c.2526C>A (p.His842Gln)
c.77-1853C>A (n.77-1853C>A)
16g.51139406T>ACA395883705SALL1c.2816A>T (p.His939Leu)
c.2525A>T (p.His842Leu)
c.77-1854A>T (n.77-1854A>T)
16g.51139406T>CCA395883703SALL1c.2816A>G (p.His939Arg)
c.2525A>G (p.His842Arg)
c.77-1854A>G (n.77-1854A>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.51139406T>GCA395883701SALL1c.2816A>C (p.His939Pro)
c.2525A>C (p.His842Pro)
c.77-1854A>C (n.77-1854A>C)
16g.51139406T=CA2222017913SALL1c.2816A= (p.His939=)
c.2525A= (p.His842=)
c.77-1854A= (n.77-1854A=)
16g.51139407G>ACA395883708SALL1c.2815C>T (p.His939Tyr)
c.2524C>T (p.His842Tyr)
c.77-1855C>T (n.77-1855C>T)
16g.51139407G>CCA395883710SALL1c.2815C>G (p.His939Asp)
c.2524C>G (p.His842Asp)
c.77-1855C>G (n.77-1855C>G)
16g.51139407G=CA2222017916SALL1c.2815C= (p.His939=)
c.2524C= (p.His842=)
c.77-1855C= (n.77-1855C=)
16g.51139407G>TCA395883712SALL1c.2815C>A (p.His939Asn)
c.2524C>A (p.His842Asn)
c.77-1855C>A (n.77-1855C>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.51139408G>ACA495780141SALL1c.2814C>T (p.Phe938=)
c.2523C>T (p.Phe841=)
c.77-1856C>T (n.77-1856C>T)
16g.51139408G>CCA395883714SALL1c.2814C>G (p.Phe938Leu)
c.2523C>G (p.Phe841Leu)
c.77-1856C>G (n.77-1856C>G)
 dbSNP
16g.51139408G=CA2222017919SALL1c.2814C= (p.Phe938=)
c.2523C= (p.Phe841=)
c.77-1856C= (n.77-1856C=)
16g.51139408G>TCA395883716SALL1c.2814C>A (p.Phe938Leu)
c.2523C>A (p.Phe841Leu)
c.77-1856C>A (n.77-1856C>A)
16g.51139409A=CA2222017922SALL1c.2813T= (p.Phe938=)
c.2522T= (p.Phe841=)
c.77-1857T= (n.77-1857T=)
16g.51139409A>CCA395883718SALL1c.2813T>G (p.Phe938Cys)
c.2522T>G (p.Phe841Cys)
c.77-1857T>G (n.77-1857T>G)
 dbSNP
16g.51139409A>GCA395883719SALL1c.2813T>C (p.Phe938Ser)
c.2522T>C (p.Phe841Ser)
c.77-1857T>C (n.77-1857T>C)
 dbSNP
16g.51139409A>TCA395883721SALL1c.2813T>A (p.Phe938Tyr)
c.2522T>A (p.Phe841Tyr)
c.77-1857T>A (n.77-1857T>A)
16g.51139410A>CCA395883723SALL1c.2812T>G (p.Phe938Val)
c.2521T>G (p.Phe841Val)
c.77-1858T>G (n.77-1858T>G)
16g.51139410A>GCA395883725SALL1c.2812T>C (p.Phe938Leu)
c.2521T>C (p.Phe841Leu)
c.77-1858T>C (n.77-1858T>C)
16g.51139410A>TCA395883726SALL1c.2812T>A (p.Phe938Ile)
c.2521T>A (p.Phe841Ile)
c.77-1858T>A (n.77-1858T>A)
16g.51139411C>ACA281301066SALL1c.2811G>T (p.Glu937Asp)
c.2520G>T (p.Glu840Asp)
c.77-1859G>T (n.77-1859G>T)
 dbSNP
16g.51139411C=CA2222017924SALL1c.2811G= (p.Glu937=)
c.2520G= (p.Glu840=)
c.77-1859G= (n.77-1859G=)
16g.51139411C>GCA395883727SALL1c.2811G>C (p.Glu937Asp)
c.2520G>C (p.Glu840Asp)
c.77-1859G>C (n.77-1859G>C)
16g.51139411C>TCA495780145SALL1c.2811G>A (p.Glu937=)
c.2520G>A (p.Glu840=)
c.77-1859G>A (n.77-1859G>A)
16g.51139412T>ACA395883731SALL1c.2810A>T (p.Glu937Val)
c.2519A>T (p.Glu840Val)
c.77-1860A>T (n.77-1860A>T)
 gnomAD v4
16g.51139412T>CCA395883732SALL1c.2810A>G (p.Glu937Gly)
c.2519A>G (p.Glu840Gly)
c.77-1860A>G (n.77-1860A>G)
16g.51139412T>GCA395883729SALL1c.2810A>C (p.Glu937Ala)
c.2519A>C (p.Glu840Ala)
c.77-1860A>C (n.77-1860A>C)
16g.51139413C>ACA395883734SALL1c.2809G>T (p.Glu937Ter)
c.2518G>T (p.Glu840Ter)
c.77-1861G>T (n.77-1861G>T)
16g.51139413C=CA2222017930SALL1c.2809G= (p.Glu937=)
c.2518G= (p.Glu840=)
c.77-1861G= (n.77-1861G=)
16g.51139413C>GCA395883735SALL1c.2809G>C (p.Glu937Gln)
c.2518G>C (p.Glu840Gln)
c.77-1861G>C (n.77-1861G>C)
 dbSNP
16g.51139413C>TCA8053034SALL1c.2809G>A (p.Glu937Lys)
c.2518G>A (p.Glu840Lys)
c.77-1861G>A (n.77-1861G>A)
 dbSNP ExAC gnomAD v4
16g.51139413_51139414delinsAACA645592649SALL1c.2808_2809delinsTT (p.Gln936HisfsTer2)
c.2517_2518delinsTT (p.Gln839HisfsTer2)
c.77-1862_77-1861delinsTT (n.77-1862_77-1861delinsTT)
 COSMIC
16g.51139414C>ACA395883737SALL1c.2808G>T (p.Gln936His)
c.2517G>T (p.Gln839His)
c.77-1862G>T (n.77-1862G>T)
 COSMIC
16g.51139414C=CA2222017933SALL1c.2808G= (p.Gln936=)
c.2517G= (p.Gln839=)
c.77-1862G= (n.77-1862G=)
16g.51139414C>GCA395883739SALL1c.2808G>C (p.Gln936His)
c.2517G>C (p.Gln839His)
c.77-1862G>C (n.77-1862G>C)
16g.51139414C>TCA8053035SALL1c.2808G>A (p.Gln936=)
c.2517G>A (p.Gln839=)
c.77-1862G>A (n.77-1862G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.51139415T>ACA395883742SALL1c.2807A>T (p.Gln936Leu)
c.2516A>T (p.Gln839Leu)
c.77-1863A>T (n.77-1863A>T)
16g.51139415T>CCA395883744SALL1c.2807A>G (p.Gln936Arg)
c.2516A>G (p.Gln839Arg)
c.77-1863A>G (n.77-1863A>G)
16g.51139415T>GCA395883746SALL1c.2807A>C (p.Gln936Pro)
c.2516A>C (p.Gln839Pro)
c.77-1863A>C (n.77-1863A>C)
16g.51139416G>ACA395883749SALL1c.2806C>T (p.Gln936Ter)
c.2515C>T (p.Gln839Ter)
c.77-1864C>T (n.77-1864C>T)
16g.51139416G>CCA395883750SALL1c.2806C>G (p.Gln936Glu)
c.2515C>G (p.Gln839Glu)
c.77-1864C>G (n.77-1864C>G)
 dbSNP gnomAD v4
16g.51139416G=CA2222017937SALL1c.2806C= (p.Gln936=)
c.2515C= (p.Gln839=)
c.77-1864C= (n.77-1864C=)
16g.51139416G>TCA395883751SALL1c.2806C>A (p.Gln936Lys)
c.2515C>A (p.Gln839Lys)
c.77-1864C>A (n.77-1864C>A)
16g.51139417C>ACA495780149SALL1c.2805G>T (p.Thr935=)
c.2514G>T (p.Thr838=)
c.77-1865G>T (n.77-1865G>T)
 dbSNP gnomAD v2 gnomAD v4
16g.51139417C=CA2222017941SALL1c.2805G= (p.Thr935=)
c.2514G= (p.Thr838=)
c.77-1865G= (n.77-1865G=)
16g.51139417C>GCA495780150SALL1c.2805G>C (p.Thr935=)
c.2514G>C (p.Thr838=)
c.77-1865G>C (n.77-1865G>C)
16g.51139417C>TCA8053036SALL1c.2805G>A (p.Thr935=)
c.2514G>A (p.Thr838=)
c.77-1865G>A (n.77-1865G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51139418G>ACA8053038SALL1c.2804C>T (p.Thr935Met)
c.2513C>T (p.Thr838Met)
c.77-1866C>T (n.77-1866C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.51139418G>CCA395883755SALL1c.2804C>G (p.Thr935Arg)
c.2513C>G (p.Thr838Arg)
c.77-1866C>G (n.77-1866C>G)
 dbSNP gnomAD v2 COSMIC
16g.51139418G=CA2222017947SALL1c.2804C= (p.Thr935=)
c.2513C= (p.Thr838=)
c.77-1866C= (n.77-1866C=)
16g.51139418G>TCA395883753SALL1c.2804C>A (p.Thr935Lys)
c.2513C>A (p.Thr838Lys)
c.77-1866C>A (n.77-1866C>A)
16g.51139419T>ACA8053039SALL1c.2803A>T (p.Thr935Ser)
c.2512A>T (p.Thr838Ser)
c.77-1867A>T (n.77-1867A>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51139419T>CCA395883761SALL1c.2803A>G (p.Thr935Ala)
c.2512A>G (p.Thr838Ala)
c.77-1867A>G (n.77-1867A>G)
16g.51139419T>GCA395883763SALL1c.2803A>C (p.Thr935Pro)
c.2512A>C (p.Thr838Pro)
c.77-1867A>C (n.77-1867A>C)
 gnomAD v4
16g.51139419T=CA2222017958SALL1c.2803A= (p.Thr935=)
c.2512A= (p.Thr838=)
c.77-1867A= (n.77-1867A=)
16g.51139421_51139426dupCA8053037SALL1c.2798_2803dup (p.Ser934_Thr935insAsnSer)
c.2507_2512dup (p.Ser837_Thr838insAsnSer)
c.77-1872_77-1867dup (n.77-1872_77-1867dup)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51139420G>ACA495780155SALL1c.2802C>T (p.Ser934=)
c.2511C>T (p.Ser837=)
c.77-1868C>T (n.77-1868C>T)
 dbSNP
16g.51139420G>CCA395883765SALL1c.2802C>G (p.Ser934Arg)
c.2511C>G (p.Ser837Arg)
c.77-1868C>G (n.77-1868C>G)
16g.51139420G=CA2222017967SALL1c.2802C= (p.Ser934=)
c.2511C= (p.Ser837=)
c.77-1868C= (n.77-1868C=)
16g.51139420G>TCA395883766SALL1c.2802C>A (p.Ser934Arg)
c.2511C>A (p.Ser837Arg)
c.77-1868C>A (n.77-1868C>A)
16g.51139420_51139421delinsGCCA2222017971SALL1c.2801_2802delinsGC (p.Ser934=)
c.2510_2511delinsGC (p.Ser837=)
c.77-1869_77-1868delinsGC (n.77-1869_77-1868delinsGC)
16g.51139421delCA915949259SALL1c.2801del (p.Ser934ThrfsTer?)
c.2510del (p.Ser837ThrfsTer?)
c.77-1869del (n.77-1869del)
 ClinVar dbSNP
16g.51139421C>ACA395883770SALL1c.2801G>T (p.Ser934Ile)
c.2510G>T (p.Ser837Ile)
c.77-1869G>T (n.77-1869G>T)
 dbSNP
16g.51139421C=CA2222017984SALL1c.2801G= (p.Ser934=)
c.2510G= (p.Ser837=)
c.77-1869G= (n.77-1869G=)
16g.51139421C>GCA395883771SALL1c.2801G>C (p.Ser934Thr)
c.2510G>C (p.Ser837Thr)
c.77-1869G>C (n.77-1869G>C)
16g.51139421C>TCA8053040SALL1c.2801G>A (p.Ser934Asn)
c.2510G>A (p.Ser837Asn)
c.77-1869G>A (n.77-1869G>A)
 dbSNP ExAC COSMIC
16g.51139422T>ACA395883775SALL1c.2800A>T (p.Ser934Cys)
c.2509A>T (p.Ser837Cys)
c.77-1870A>T (n.77-1870A>T)
16g.51139422T>CCA395883777SALL1c.2800A>G (p.Ser934Gly)
c.2509A>G (p.Ser837Gly)
c.77-1870A>G (n.77-1870A>G)
 ClinVar gnomAD v4
16g.51139422T>GCA395883779SALL1c.2800A>C (p.Ser934Arg)
c.2509A>C (p.Ser837Arg)
c.77-1870A>C (n.77-1870A>C)
16g.51139423G>ACA495780159SALL1c.2799C>T (p.Asn933=)
c.2508C>T (p.Asn836=)
c.77-1871C>T (n.77-1871C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.51139423G>CCA395883780SALL1c.2799C>G (p.Asn933Lys)
c.2508C>G (p.Asn836Lys)
c.77-1871C>G (n.77-1871C>G)
16g.51139423G=CA2222017990SALL1c.2799C= (p.Asn933=)
c.2508C= (p.Asn836=)
c.77-1871C= (n.77-1871C=)
16g.51139423G>TCA395883781SALL1c.2799C>A (p.Asn933Lys)
c.2508C>A (p.Asn836Lys)
c.77-1871C>A (n.77-1871C>A)
16g.51139424T>ACA395883785SALL1c.2798A>T (p.Asn933Ile)
c.2507A>T (p.Asn836Ile)
c.77-1872A>T (n.77-1872A>T)
16g.51139424T>CCA8053041SALL1c.2798A>G (p.Asn933Ser)
c.2507A>G (p.Asn836Ser)
c.77-1872A>G (n.77-1872A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51139424T>GCA395883782SALL1c.2798A>C (p.Asn933Thr)
c.2507A>C (p.Asn836Thr)
c.77-1872A>C (n.77-1872A>C)
 dbSNP
16g.51139424T=CA2222017999SALL1c.2798A= (p.Asn933=)
c.2507A= (p.Asn836=)
c.77-1872A= (n.77-1872A=)
16g.51139425T>ACA395883788SALL1c.2797A>T (p.Asn933Tyr)
c.2506A>T (p.Asn836Tyr)
c.77-1873A>T (n.77-1873A>T)
16g.51139425T>CCA395883790SALL1c.2797A>G (p.Asn933Asp)
c.2506A>G (p.Asn836Asp)
c.77-1873A>G (n.77-1873A>G)
 gnomAD v4
16g.51139425T>GCA395883792SALL1c.2797A>C (p.Asn933His)
c.2506A>C (p.Asn836His)
c.77-1873A>C (n.77-1873A>C)
16g.51139426G>ACA495780161SALL1c.2796C>T (p.Ser932=)
c.2505C>T (p.Ser835=)
c.77-1874C>T (n.77-1874C>T)
 gnomAD v4 COSMIC
16g.51139426G>CCA495780162SALL1c.2796C>G (p.Ser932=)
c.2505C>G (p.Ser835=)
c.77-1874C>G (n.77-1874C>G)
16g.51139426G=CA2222018004SALL1c.2796C= (p.Ser932=)
c.2505C= (p.Ser835=)
c.77-1874C= (n.77-1874C=)
16g.51139426G>TCA8053042SALL1c.2796C>A (p.Ser932=)
c.2505C>A (p.Ser835=)
c.77-1874C>A (n.77-1874C>A)
 dbSNP ExAC gnomAD v2
16g.51139427G>ACA395883795SALL1c.2795C>T (p.Ser932Phe)
c.2504C>T (p.Ser835Phe)
c.77-1875C>T (n.77-1875C>T)
16g.51139427G>CCA395883797SALL1c.2795C>G (p.Ser932Cys)
c.2504C>G (p.Ser835Cys)
c.77-1875C>G (n.77-1875C>G)
16g.51139427G>TCA395883798SALL1c.2795C>A (p.Ser932Tyr)
c.2504C>A (p.Ser835Tyr)
c.77-1875C>A (n.77-1875C>A)
 COSMIC
16g.51139428A>CCA395883804SALL1c.2794T>G (p.Ser932Ala)
c.2503T>G (p.Ser835Ala)
c.77-1876T>G (n.77-1876T>G)
16g.51139428A>GCA395883800SALL1c.2794T>C (p.Ser932Pro)
c.2503T>C (p.Ser835Pro)
c.77-1876T>C (n.77-1876T>C)
16g.51139428A>TCA395883802SALL1c.2794T>A (p.Ser932Thr)
c.2503T>A (p.Ser835Thr)
c.77-1876T>A (n.77-1876T>A)
16g.51139429C>ACA495780163SALL1c.2793G>T (p.Pro931=)
c.2502G>T (p.Pro834=)
c.77-1877G>T (n.77-1877G>T)
16g.51139429C=CA2222018008SALL1c.2793G= (p.Pro931=)
c.2502G= (p.Pro834=)
c.77-1877G= (n.77-1877G=)
16g.51139429C>GCA8053044SALL1c.2793G>C (p.Pro931=)
c.2502G>C (p.Pro834=)
c.77-1877G>C (n.77-1877G>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51139429C>TCA8053043SALL1c.2793G>A (p.Pro931=)
c.2502G>A (p.Pro834=)
c.77-1877G>A (n.77-1877G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51139430G>ACA8053045SALL1c.2792C>T (p.Pro931Leu)
c.2501C>T (p.Pro834Leu)
c.77-1878C>T (n.77-1878C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.51139430G>CCA395883811SALL1c.2792C>G (p.Pro931Arg)
c.2501C>G (p.Pro834Arg)
c.77-1878C>G (n.77-1878C>G)
16g.51139430G=CA2222018017SALL1c.2792C= (p.Pro931=)
c.2501C= (p.Pro834=)
c.77-1878C= (n.77-1878C=)
16g.51139430G>TCA395883812SALL1c.2792C>A (p.Pro931Gln)
c.2501C>A (p.Pro834Gln)
c.77-1878C>A (n.77-1878C>A)
 COSMIC
16g.51139431G>ACA395883815SALL1c.2791C>T (p.Pro931Ser)
c.2500C>T (p.Pro834Ser)
c.77-1879C>T (n.77-1879C>T)
16g.51139431G>CCA395883818SALL1c.2791C>G (p.Pro931Ala)
c.2500C>G (p.Pro834Ala)
c.77-1879C>G (n.77-1879C>G)
 gnomAD v4
16g.51139431G>TCA395883816SALL1c.2791C>A (p.Pro931Thr)
c.2500C>A (p.Pro834Thr)
c.77-1879C>A (n.77-1879C>A)
16g.51139432G>ACA495780165SALL1c.2790C>T (p.Ser930=)
c.2499C>T (p.Ser833=)
c.77-1880C>T (n.77-1880C>T)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
16g.51139432G>CCA495780166SALL1c.2790C>G (p.Ser930=)
c.2499C>G (p.Ser833=)
c.77-1880C>G (n.77-1880C>G)
16g.51139432G=CA2222018022SALL1c.2790C= (p.Ser930=)
c.2499C= (p.Ser833=)
c.77-1880C= (n.77-1880C=)
16g.51139432G>TCA495780167SALL1c.2790C>A (p.Ser930=)
c.2499C>A (p.Ser833=)
c.77-1880C>A (n.77-1880C>A)
16g.51139433G>ACA395883821SALL1c.2789C>T (p.Ser930Phe)
c.2498C>T (p.Ser833Phe)
c.77-1881C>T (n.77-1881C>T)
16g.51139433G>CCA395883822SALL1c.2789C>G (p.Ser930Cys)
c.2498C>G (p.Ser833Cys)
c.77-1881C>G (n.77-1881C>G)
 dbSNP gnomAD v3 gnomAD v4
16g.51139433G=CA2222018025SALL1c.2789C= (p.Ser930=)
c.2498C= (p.Ser833=)
c.77-1881C= (n.77-1881C=)
16g.51139433G>TCA395883824SALL1c.2789C>A (p.Ser930Tyr)
c.2498C>A (p.Ser833Tyr)
c.77-1881C>A (n.77-1881C>A)
16g.51139434A=CA2222018029SALL1c.2788T= (p.Ser930=)
c.2497T= (p.Ser833=)
c.77-1882T= (n.77-1882T=)
16g.51139434A>CCA395883826SALL1c.2788T>G (p.Ser930Ala)
c.2497T>G (p.Ser833Ala)
c.77-1882T>G (n.77-1882T>G)
16g.51139434A>GCA395883828SALL1c.2788T>C (p.Ser930Pro)
c.2497T>C (p.Ser833Pro)
c.77-1882T>C (n.77-1882T>C)
16g.51139434A>TCA395883830SALL1c.2788T>A (p.Ser930Thr)
c.2497T>A (p.Ser833Thr)
c.77-1882T>A (n.77-1882T>A)
 dbSNP
16g.51139435C>ACA495780169SALL1c.2787G>T (p.Leu929=)
c.2496G>T (p.Leu832=)
c.77-1883G>T (n.77-1883G>T)
 gnomAD v4
16g.51139435C=CA2222018034SALL1c.2787G= (p.Leu929=)
c.2496G= (p.Leu832=)
c.77-1883G= (n.77-1883G=)
16g.51139435C>GCA495780170SALL1c.2787G>C (p.Leu929=)
c.2496G>C (p.Leu832=)
c.77-1883G>C (n.77-1883G>C)
16g.51139435C>TCA495780171SALL1c.2787G>A (p.Leu929=)
c.2496G>A (p.Leu832=)
c.77-1883G>A (n.77-1883G>A)
 dbSNP gnomAD v2
16g.51139436A>CCA395883833SALL1c.2786T>G (p.Leu929Arg)
c.2495T>G (p.Leu832Arg)
c.77-1884T>G (n.77-1884T>G)
16g.51139436A>GCA395883835SALL1c.2786T>C (p.Leu929Pro)
c.2495T>C (p.Leu832Pro)
c.77-1884T>C (n.77-1884T>C)
16g.51139436A>TCA395883837SALL1c.2786T>A (p.Leu929Gln)
c.2495T>A (p.Leu832Gln)
c.77-1884T>A (n.77-1884T>A)
16g.51139437G>ACA495780172SALL1c.2785C>T (p.Leu929=)
c.2494C>T (p.Leu832=)
c.77-1885C>T (n.77-1885C>T)
16g.51139437G>CCA395883839SALL1c.2785C>G (p.Leu929Val)
c.2494C>G (p.Leu832Val)
c.77-1885C>G (n.77-1885C>G)
 gnomAD v4
16g.51139437G>TCA395883841SALL1c.2785C>A (p.Leu929Met)
c.2494C>A (p.Leu832Met)
c.77-1885C>A (n.77-1885C>A)
16g.51139438A>CCA495780173SALL1c.2784T>G (p.Ala928=)
c.2493T>G (p.Ala831=)
c.77-1886T>G (n.77-1886T>G)
16g.51139438A>GCA495780174SALL1c.2784T>C (p.Ala928=)
c.2493T>C (p.Ala831=)
c.77-1886T>C (n.77-1886T>C)
16g.51139438A>TCA495780176SALL1c.2784T>A (p.Ala928=)
c.2493T>A (p.Ala831=)
c.77-1886T>A (n.77-1886T>A)
16g.51139439G>ACA395883843SALL1c.2783C>T (p.Ala928Val)
c.2492C>T (p.Ala831Val)
c.77-1887C>T (n.77-1887C>T)
16g.51139439G>CCA395883845SALL1c.2783C>G (p.Ala928Gly)
c.2492C>G (p.Ala831Gly)
c.77-1887C>G (n.77-1887C>G)
16g.51139439G>TCA395883844SALL1c.2783C>A (p.Ala928Asp)
c.2492C>A (p.Ala831Asp)
c.77-1887C>A (n.77-1887C>A)
16g.51139440C>ACA395883847SALL1c.2782G>T (p.Ala928Ser)
c.2491G>T (p.Ala831Ser)
c.77-1888G>T (n.77-1888G>T)
 gnomAD v4
16g.51139440C>GCA395883851SALL1c.2782G>C (p.Ala928Pro)
c.2491G>C (p.Ala831Pro)
c.77-1888G>C (n.77-1888G>C)
 gnomAD v4
16g.51139440C>TCA395883849SALL1c.2782G>A (p.Ala928Thr)
c.2491G>A (p.Ala831Thr)
c.77-1888G>A (n.77-1888G>A)
16g.51139441C>ACA395883853SALL1c.2781G>T (p.Gln927His)
c.2490G>T (p.Gln830His)
c.77-1889G>T (n.77-1889G>T)
16g.51139441C>GCA395883855SALL1c.2781G>C (p.Gln927His)
c.2490G>C (p.Gln830His)
c.77-1889G>C (n.77-1889G>C)
16g.51139441C>TCA495780178SALL1c.2781G>A (p.Gln927=)
c.2490G>A (p.Gln830=)
c.77-1889G>A (n.77-1889G>A)
16g.51139442T>ACA395883857SALL1c.2780A>T (p.Gln927Leu)
c.2489A>T (p.Gln830Leu)
c.77-1890A>T (n.77-1890A>T)
16g.51139442T>CCA395883858SALL1c.2780A>G (p.Gln927Arg)
c.2489A>G (p.Gln830Arg)
c.77-1890A>G (n.77-1890A>G)
 ClinVar dbSNP gnomAD v4
16g.51139442T>GCA395883860SALL1c.2780A>C (p.Gln927Pro)
c.2489A>C (p.Gln830Pro)
c.77-1890A>C (n.77-1890A>C)
16g.51139442T=CA2222018037SALL1c.2780A= (p.Gln927=)
c.2489A= (p.Gln830=)
c.77-1890A= (n.77-1890A=)
16g.51139443G>ACA395883862SALL1c.2779C>T (p.Gln927Ter)
c.2488C>T (p.Gln830Ter)
c.77-1891C>T (n.77-1891C>T)
16g.51139443G>CCA395883864SALL1c.2779C>G (p.Gln927Glu)
c.2488C>G (p.Gln830Glu)
c.77-1891C>G (n.77-1891C>G)
16g.51139443G>TCA395883867SALL1c.2779C>A (p.Gln927Lys)
c.2488C>A (p.Gln830Lys)
c.77-1891C>A (n.77-1891C>A)
16g.51139444C>ACA395883871SALL1c.2778G>T (p.Met926Ile)
c.2487G>T (p.Met829Ile)
c.77-1892G>T (n.77-1892G>T)
 gnomAD v4
16g.51139444C>GCA395883873SALL1c.2778G>C (p.Met926Ile)
c.2487G>C (p.Met829Ile)
c.77-1892G>C (n.77-1892G>C)
16g.51139444C>TCA395883875SALL1c.2778G>A (p.Met926Ile)
c.2487G>A (p.Met829Ile)
c.77-1892G>A (n.77-1892G>A)
16g.51139445A>CCA395883881SALL1c.2777T>G (p.Met926Arg)
c.2486T>G (p.Met829Arg)
c.77-1893T>G (n.77-1893T>G)
16g.51139445A>GCA395883879SALL1c.2777T>C (p.Met926Thr)
c.2486T>C (p.Met829Thr)
c.77-1893T>C (n.77-1893T>C)
16g.51139445A>TCA395883877SALL1c.2777T>A (p.Met926Lys)
c.2486T>A (p.Met829Lys)
c.77-1893T>A (n.77-1893T>A)
16g.51139446T>ACA395883883SALL1c.2776A>T (p.Met926Leu)
c.2485A>T (p.Met829Leu)
c.77-1894A>T (n.77-1894A>T)
 dbSNP gnomAD v4
16g.51139446T>CCA395883885SALL1c.2776A>G (p.Met926Val)
c.2485A>G (p.Met829Val)
c.77-1894A>G (n.77-1894A>G)
 dbSNP gnomAD v4
16g.51139446T>GCA395883887SALL1c.2776A>C (p.Met926Leu)
c.2485A>C (p.Met829Leu)
c.77-1894A>C (n.77-1894A>C)
16g.51139446T=CA2222018042SALL1c.2776A= (p.Met926=)
c.2485A= (p.Met829=)
c.77-1894A= (n.77-1894A=)
16g.51139447G>ACA495780181SALL1c.2775C>T (p.Ser925=)
c.2484C>T (p.Ser828=)
c.77-1895C>T (n.77-1895C>T)
16g.51139447G>CCA495780182SALL1c.2775C>G (p.Ser925=)
c.2484C>G (p.Ser828=)
c.77-1895C>G (n.77-1895C>G)
16g.51139447G>TCA495780183SALL1c.2775C>A (p.Ser925=)
c.2484C>A (p.Ser828=)
c.77-1895C>A (n.77-1895C>A)
16g.51139448G>ACA395883890SALL1c.2774C>T (p.Ser925Phe)
c.2483C>T (p.Ser828Phe)
c.77-1896C>T (n.77-1896C>T)
16g.51139448G>CCA395883892SALL1c.2774C>G (p.Ser925Cys)
c.2483C>G (p.Ser828Cys)
c.77-1896C>G (n.77-1896C>G)
16g.51139448G>TCA395883894SALL1c.2774C>A (p.Ser925Tyr)
c.2483C>A (p.Ser828Tyr)
c.77-1896C>A (n.77-1896C>A)
16g.51139449A>CCA395883896SALL1c.2773T>G (p.Ser925Ala)
c.2482T>G (p.Ser828Ala)
c.77-1897T>G (n.77-1897T>G)
16g.51139449A>GCA395883898SALL1c.2773T>C (p.Ser925Pro)
c.2482T>C (p.Ser828Pro)
c.77-1897T>C (n.77-1897T>C)
16g.51139449A>TCA395883899SALL1c.2773T>A (p.Ser925Thr)
c.2482T>A (p.Ser828Thr)
c.77-1897T>A (n.77-1897T>A)
16g.51139450A>CCA495780185SALL1c.2772T>G (p.Ser924=)
c.2481T>G (p.Ser827=)
c.77-1898T>G (n.77-1898T>G)
16g.51139450A>GCA495780186SALL1c.2772T>C (p.Ser924=)
c.2481T>C (p.Ser827=)
c.77-1898T>C (n.77-1898T>C)
16g.51139450A>TCA495780187SALL1c.2772T>A (p.Ser924=)
c.2481T>A (p.Ser827=)
c.77-1898T>A (n.77-1898T>A)
16g.51139451G>ACA395883902SALL1c.2771C>T (p.Ser924Phe)
c.2480C>T (p.Ser827Phe)
c.77-1899C>T (n.77-1899C>T)
 COSMIC
16g.51139451G>CCA395883904SALL1c.2771C>G (p.Ser924Cys)
c.2480C>G (p.Ser827Cys)
c.77-1899C>G (n.77-1899C>G)
16g.51139451G>TCA395883906SALL1c.2771C>A (p.Ser924Tyr)
c.2480C>A (p.Ser827Tyr)
c.77-1899C>A (n.77-1899C>A)
16g.51139452A>CCA395883913SALL1c.2770T>G (p.Ser924Ala)
c.2479T>G (p.Ser827Ala)
c.77-1900T>G (n.77-1900T>G)
16g.51139452A>GCA395883910SALL1c.2770T>C (p.Ser924Pro)
c.2479T>C (p.Ser827Pro)
c.77-1900T>C (n.77-1900T>C)
16g.51139452A>TCA395883909SALL1c.2770T>A (p.Ser924Thr)
c.2479T>A (p.Ser827Thr)
c.77-1900T>A (n.77-1900T>A)
16g.51139453G>ACA495780188SALL1c.2769C>T (p.Thr923=)
c.2478C>T (p.Thr826=)
c.77-1901C>T (n.77-1901C>T)
16g.51139453G>CCA495780190SALL1c.2769C>G (p.Thr923=)
c.2478C>G (p.Thr826=)
c.77-1901C>G (n.77-1901C>G)
16g.51139453G>TCA495780189SALL1c.2769C>A (p.Thr923=)
c.2478C>A (p.Thr826=)
c.77-1901C>A (n.77-1901C>A)
16g.51139454G>ACA395883914SALL1c.2768C>T (p.Thr923Ile)
c.2477C>T (p.Thr826Ile)
c.77-1902C>T (n.77-1902C>T)
16g.51139454G>CCA395883917SALL1c.2768C>G (p.Thr923Ser)
c.2477C>G (p.Thr826Ser)
c.77-1902C>G (n.77-1902C>G)
 dbSNP
16g.51139454G=CA2222018051SALL1c.2768C= (p.Thr923=)
c.2477C= (p.Thr826=)
c.77-1902C= (n.77-1902C=)
16g.51139454G>TCA395883919SALL1c.2768C>A (p.Thr923Asn)
c.2477C>A (p.Thr826Asn)
c.77-1902C>A (n.77-1902C>A)
16g.51139455T>ACA8053046SALL1c.2767A>T (p.Thr923Ser)
c.2476A>T (p.Thr826Ser)
c.77-1903A>T (n.77-1903A>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51139455T>CCA395883922SALL1c.2767A>G (p.Thr923Ala)
c.2476A>G (p.Thr826Ala)
c.77-1903A>G (n.77-1903A>G)
 ClinVar dbSNP gnomAD v4
16g.51139455T>GCA395883924SALL1c.2767A>C (p.Thr923Pro)
c.2476A>C (p.Thr826Pro)
c.77-1903A>C (n.77-1903A>C)
 dbSNP
16g.51139455T=CA2222018060SALL1c.2767A= (p.Thr923=)
c.2476A= (p.Thr826=)
c.77-1903A= (n.77-1903A=)
16g.51139456A>CCA495780194SALL1c.2766T>G (p.Ser922=)
c.2475T>G (p.Ser825=)
c.77-1904T>G (n.77-1904T>G)
16g.51139456A>GCA495780193SALL1c.2766T>C (p.Ser922=)
c.2475T>C (p.Ser825=)
c.77-1904T>C (n.77-1904T>C)
16g.51139456A>TCA495780192SALL1c.2766T>A (p.Ser922=)
c.2475T>A (p.Ser825=)
c.77-1904T>A (n.77-1904T>A)
16g.51139457G>ACA395883930SALL1c.2765C>T (p.Ser922Phe)
c.2474C>T (p.Ser825Phe)
c.77-1905C>T (n.77-1905C>T)
16g.51139457G>CCA395883927SALL1c.2765C>G (p.Ser922Cys)
c.2474C>G (p.Ser825Cys)
c.77-1905C>G (n.77-1905C>G)
 dbSNP gnomAD v3 gnomAD v4
16g.51139457G=CA2222018071SALL1c.2765C= (p.Ser922=)
c.2474C= (p.Ser825=)
c.77-1905C= (n.77-1905C=)
16g.51139457G>TCA395883929SALL1c.2765C>A (p.Ser922Tyr)
c.2474C>A (p.Ser825Tyr)
c.77-1905C>A (n.77-1905C>A)
16g.51139458A=CA2222018076SALL1c.2764T= (p.Ser922=)
c.2473T= (p.Ser825=)
c.77-1906T= (n.77-1906T=)
16g.51139458A>CCA395883933SALL1c.2764T>G (p.Ser922Ala)
c.2473T>G (p.Ser825Ala)
c.77-1906T>G (n.77-1906T>G)
16g.51139458A>GCA395883934SALL1c.2764T>C (p.Ser922Pro)
c.2473T>C (p.Ser825Pro)
c.77-1906T>C (n.77-1906T>C)
 dbSNP
16g.51139458A>TCA395883936SALL1c.2764T>A (p.Ser922Thr)
c.2473T>A (p.Ser825Thr)
c.77-1906T>A (n.77-1906T>A)
16g.51139459C>ACA395883938SALL1c.2763G>T (p.Glu921Asp)
c.2472G>T (p.Glu824Asp)
c.77-1907G>T (n.77-1907G>T)
16g.51139459C>GCA395883940SALL1c.2763G>C (p.Glu921Asp)
c.2472G>C (p.Glu824Asp)
c.77-1907G>C (n.77-1907G>C)
16g.51139459C>TCA495780198SALL1c.2763G>A (p.Glu921=)
c.2472G>A (p.Glu824=)
c.77-1907G>A (n.77-1907G>A)
16g.51139460T>ACA395883942SALL1c.2762A>T (p.Glu921Val)
c.2471A>T (p.Glu824Val)
c.77-1908A>T (n.77-1908A>T)
16g.51139460T>CCA395883944SALL1c.2762A>G (p.Glu921Gly)
c.2471A>G (p.Glu824Gly)
c.77-1908A>G (n.77-1908A>G)
16g.51139460T>GCA395883943SALL1c.2762A>C (p.Glu921Ala)
c.2471A>C (p.Glu824Ala)
c.77-1908A>C (n.77-1908A>C)
16g.51139461C>ACA395883945SALL1c.2761G>T (p.Glu921Ter)
c.2470G>T (p.Glu824Ter)
c.77-1909G>T (n.77-1909G>T)
16g.51139461C>GCA395883946SALL1c.2761G>C (p.Glu921Gln)
c.2470G>C (p.Glu824Gln)
c.77-1909G>C (n.77-1909G>C)
16g.51139461C>TCA395883947SALL1c.2761G>A (p.Glu921Lys)
c.2470G>A (p.Glu824Lys)
c.77-1909G>A (n.77-1909G>A)
16g.51139462T>ACA495780199SALL1c.2760A>T (p.Ser920=)
c.2469A>T (p.Ser823=)
c.77-1910A>T (n.77-1910A>T)
16g.51139462T>CCA495780200SALL1c.2760A>G (p.Ser920=)
c.2469A>G (p.Ser823=)
c.77-1910A>G (n.77-1910A>G)
16g.51139462T>GCA495780201SALL1c.2760A>C (p.Ser920=)
c.2469A>C (p.Ser823=)
c.77-1910A>C (n.77-1910A>C)
16g.51139463G>ACA395883948SALL1c.2759C>T (p.Ser920Leu)
c.2468C>T (p.Ser823Leu)
c.77-1911C>T (n.77-1911C>T)
16g.51139463G>CCA395883949SALL1c.2759C>G (p.Ser920Ter)
c.2468C>G (p.Ser823Ter)
c.77-1911C>G (n.77-1911C>G)
16g.51139463G>TCA395883950SALL1c.2759C>A (p.Ser920Ter)
c.2468C>A (p.Ser823Ter)
c.77-1911C>A (n.77-1911C>A)
16g.51139464A>CCA395883951SALL1c.2758T>G (p.Ser920Ala)
c.2467T>G (p.Ser823Ala)
c.77-1912T>G (n.77-1912T>G)
16g.51139464A>GCA395883952SALL1c.2758T>C (p.Ser920Pro)
c.2467T>C (p.Ser823Pro)
c.77-1912T>C (n.77-1912T>C)
16g.51139464A>TCA395883953SALL1c.2758T>A (p.Ser920Thr)
c.2467T>A (p.Ser823Thr)
c.77-1912T>A (n.77-1912T>A)
16g.51139465G>ACA495780202SALL1c.2757C>T (p.Ile919=)
c.2466C>T (p.Ile822=)
c.77-1913C>T (n.77-1913C>T)
 gnomAD v4
16g.51139465G>CCA395883954SALL1c.2757C>G (p.Ile919Met)
c.2466C>G (p.Ile822Met)
c.77-1913C>G (n.77-1913C>G)
16g.51139465G>TCA495780203SALL1c.2757C>A (p.Ile919=)
c.2466C>A (p.Ile822=)
c.77-1913C>A (n.77-1913C>A)
16g.51139466A>CCA395883957SALL1c.2756T>G (p.Ile919Ser)
c.2465T>G (p.Ile822Ser)
c.77-1914T>G (n.77-1914T>G)
16g.51139466A>GCA395883956SALL1c.2756T>C (p.Ile919Thr)
c.2465T>C (p.Ile822Thr)
c.77-1914T>C (n.77-1914T>C)
16g.51139466A>TCA395883955SALL1c.2756T>A (p.Ile919Asn)
c.2465T>A (p.Ile822Asn)
c.77-1914T>A (n.77-1914T>A)
16g.51139467T>ACA395883958SALL1c.2755A>T (p.Ile919Phe)
c.2464A>T (p.Ile822Phe)
c.77-1915A>T (n.77-1915A>T)
16g.51139467T>CCA395883960SALL1c.2755A>G (p.Ile919Val)
c.2464A>G (p.Ile822Val)
c.77-1915A>G (n.77-1915A>G)
 dbSNP gnomAD v3 gnomAD v4
16g.51139467T>GCA395883959SALL1c.2755A>C (p.Ile919Leu)
c.2464A>C (p.Ile822Leu)
c.77-1915A>C (n.77-1915A>C)
16g.51139467T=CA2222018080SALL1c.2755A= (p.Ile919=)
c.2464A= (p.Ile822=)
c.77-1915A= (n.77-1915A=)
16g.51139468G>ACA8053047SALL1c.2754C>T (p.Ala918=)
c.2463C>T (p.Ala821=)
c.77-1916C>T (n.77-1916C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.51139468G>CCA495780205SALL1c.2754C>G (p.Ala918=)
c.2463C>G (p.Ala821=)
c.77-1916C>G (n.77-1916C>G)
16g.51139468G=CA2222018084SALL1c.2754C= (p.Ala918=)
c.2463C= (p.Ala821=)
c.77-1916C= (n.77-1916C=)
16g.51139468G>TCA495780206SALL1c.2754C>A (p.Ala918=)
c.2463C>A (p.Ala821=)
c.77-1916C>A (n.77-1916C>A)

Number of alleles fetched