Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.8073781_8073947del | CA645553620 | GATA3 | c.1090_1256del (p.Arg364HisfsTer?) c.1093_1259del (p.Arg365HisfsTer?) n.612_778del | COSMIC |
10 | g.8073883_8073904delinsGG | CA2580650497 | GATA3 | c.1192_1213delinsGG (p.Arg398GlyfsTer?) c.1195_1216delinsGG (p.Arg399GlyfsTer?) n.714_735delinsGG | |
10 | g.8073888_8073889del | CA2695211824 | GATA3 | c.1197_1198del (p.Met400ValfsTer?) c.1200_1201del (p.Met401ValfsTer?) n.719_720del | |
10 | g.8073888_8073890delinsCAT | CA1888996085 | GATA3 | c.1197_1199delinsCAT (p.His399=) c.1200_1202delinsCAT (p.His400=) n.719_721delinsCAT | |
10 | g.8073890_8073905dup | CA645553627 | GATA3 | c.1199_1214dup (p.Ile406ValfsTer?) c.1202_1217dup (p.Ile407ValfsTer?) n.721_736dup | COSMIC |
10 | g.8073889A= | CA1888996098 | GATA3 | c.1198A= (p.Met400=) c.1201A= (p.Met401=) n.720A= | |
10 | g.8073889A>C | CA375975753 | GATA3 | c.1198A>C (p.Met400Leu) c.1201A>C (p.Met401Leu) n.720A>C | dbSNP gnomAD v4 |
10 | g.8073889A>G | CA375975755 | GATA3 | c.1198A>G (p.Met400Val) c.1201A>G (p.Met401Val) n.720A>G | dbSNP gnomAD v3 gnomAD v4 |
10 | g.8073889A>T | CA375975754 | GATA3 | c.1198A>T (p.Met400Leu) c.1201A>T (p.Met401Leu) n.720A>T | dbSNP gnomAD v4 |
10 | g.8073889dup | CA468400969 | GATA3 | c.1198dup (p.Met400AsnfsTer?) c.1201dup (p.Met401AsnfsTer?) n.720dup | COSMIC |
10 | g.8073889_8073890del | CA645294058 | GATA3 | c.1198_1199del (p.Met400ValfsTer?) c.1201_1202del (p.Met401ValfsTer?) n.720_721del | ClinVar dbSNP COSMIC |
10 | g.8073890T>A | CA375975756 | GATA3 | c.1199T>A (p.Met400Lys) c.1202T>A (p.Met401Lys) n.721T>A | dbSNP |
10 | g.8073890T>C | CA375975757 | GATA3 | c.1199T>C (p.Met400Thr) c.1202T>C (p.Met401Thr) n.721T>C | dbSNP gnomAD v3 gnomAD v4 |
10 | g.8073890T>G | CA375975758 | GATA3 | c.1199T>G (p.Met400Arg) c.1202T>G (p.Met401Arg) n.721T>G | |
10 | g.8073890T= | CA1888996102 | GATA3 | c.1199T= (p.Met400=) c.1202T= (p.Met401=) n.721T= | |
10 | g.8073890_8073891insA | CA468400971 | GATA3 | c.1199_1200insA (p.Met400IlefsTer?) c.1202_1203insA (p.Met401IlefsTer?) n.721_722insA | |
10 | g.8073891G>A | CA375975759 | GATA3 | c.1200G>A (p.Met400Ile) c.1203G>A (p.Met401Ile) n.722G>A | ClinVar |
10 | g.8073891G>C | CA375975760 | GATA3 | c.1200G>C (p.Met400Ile) c.1203G>C (p.Met401Ile) n.722G>C | dbSNP |
10 | g.8073891G>T | CA375975761 | GATA3 | c.1200G>T (p.Met400Ile) c.1203G>T (p.Met401Ile) n.722G>T | dbSNP |
10 | g.8073891dup | CA468400972 | GATA3 | c.1200dup (p.Ser401ValfsTer?) c.1203dup (p.Ser402ValfsTer?) n.722dup | COSMIC |
10 | g.8073892T>A | CA375975762 | GATA3 | c.1201T>A (p.Ser401Thr) c.1204T>A (p.Ser402Thr) n.723T>A | |
10 | g.8073892T>C | CA375975763 | GATA3 | c.1201T>C (p.Ser401Pro) c.1204T>C (p.Ser402Pro) n.723T>C | |
10 | g.8073892T>G | CA375975764 | GATA3 | c.1201T>G (p.Ser401Ala) c.1204T>G (p.Ser402Ala) n.723T>G | gnomAD v4 |
10 | g.8073892_8073895dup | CA645553629 | GATA3 | c.1201_1204dup (p.Ser402PhefsTer?) c.1204_1207dup (p.Ser403PhefsTer?) n.723_726dup | COSMIC COSMIC |
10 | g.8073893C>A | CA375975765 | GATA3 | c.1202C>A (p.Ser401Tyr) c.1205C>A (p.Ser402Tyr) n.724C>A | |
10 | g.8073893C>G | CA375975766 | GATA3 | c.1202C>G (p.Ser401Cys) c.1205C>G (p.Ser402Cys) n.724C>G | dbSNP |
10 | g.8073893C>T | CA375975767 | GATA3 | c.1202C>T (p.Ser401Phe) c.1205C>T (p.Ser402Phe) n.724C>T | dbSNP |
10 | g.8073894dup | CA645553630 | GATA3 | c.1203dup (p.Ser402LeufsTer?) c.1206dup (p.Ser403LeufsTer?) n.725dup | COSMIC |
10 | g.8073894C>A | CA468400976 | GATA3 | c.1203C>A (p.Ser401=) c.1206C>A (p.Ser402=) n.725C>A | dbSNP |
10 | g.8073894C= | CA1888996105 | GATA3 | c.1203C= (p.Ser401=) c.1206C= (p.Ser402=) n.725C= | |
10 | g.8073894C>G | CA5404567 | GATA3 | c.1203C>G (p.Ser401=) c.1206C>G (p.Ser402=) n.725C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.8073894C>T | CA468400977 | GATA3 | c.1203C>T (p.Ser401=) c.1206C>T (p.Ser402=) n.725C>T | dbSNP |
10 | g.8073895T>A | CA375975768 | GATA3 | c.1204T>A (p.Ser402Thr) c.1207T>A (p.Ser403Thr) n.726T>A | |
10 | g.8073895T>C | CA375975769 | GATA3 | c.1204T>C (p.Ser402Pro) c.1207T>C (p.Ser403Pro) n.726T>C | |
10 | g.8073895T>G | CA375975770 | GATA3 | c.1204T>G (p.Ser402Ala) c.1207T>G (p.Ser403Ala) n.726T>G | |
10 | g.8073896C>A | CA375975771 | GATA3 | c.1205C>A (p.Ser402Tyr) c.1208C>A (p.Ser403Tyr) n.727C>A | dbSNP |
10 | g.8073896C>G | CA375975772 | GATA3 | c.1205C>G (p.Ser402Cys) c.1208C>G (p.Ser403Cys) n.727C>G | dbSNP |
10 | g.8073896C>T | CA375975773 | GATA3 | c.1205C>T (p.Ser402Phe) c.1208C>T (p.Ser403Phe) n.727C>T | dbSNP |
10 | g.8073898dup | CA468400981 | GATA3 | c.1207dup (p.Leu403ProfsTer?) c.1210dup (p.Leu404ProfsTer?) n.729dup | |
10 | g.8073897C>A | CA468400983 | GATA3 | c.1206C>A (p.Ser402=) c.1209C>A (p.Ser403=) n.728C>A | dbSNP |
10 | g.8073897C>G | CA468400985 | GATA3 | c.1206C>G (p.Ser402=) c.1209C>G (p.Ser403=) n.728C>G | dbSNP |
10 | g.8073897C>T | CA468400986 | GATA3 | c.1206C>T (p.Ser402=) c.1209C>T (p.Ser403=) n.728C>T | dbSNP COSMIC |
10 | g.8073898C>A | CA375975774 | GATA3 | c.1207C>A (p.Leu403Met) c.1210C>A (p.Leu404Met) n.729C>A | |
10 | g.8073898C= | CA1888996108 | GATA3 | c.1207C= (p.Leu403=) c.1210C= (p.Leu404=) n.729C= | |
10 | g.8073898C>G | CA375975775 | GATA3 | c.1207C>G (p.Leu403Val) c.1210C>G (p.Leu404Val) n.729C>G | dbSNP |
10 | g.8073898C>T | CA468400988 | GATA3 | c.1207C>T (p.Leu403=) c.1210C>T (p.Leu404=) n.729C>T | dbSNP gnomAD v2 gnomAD v4 |
10 | g.8073898_8073899del | CA645553631 | GATA3 | c.1207_1208del (p.Leu403GlufsTer?) c.1210_1211del (p.Leu404GlufsTer?) n.729_730del | COSMIC |
10 | g.8073899T>A | CA375975776 | GATA3 | c.1208T>A (p.Leu403Gln) c.1211T>A (p.Leu404Gln) n.730T>A | |
10 | g.8073899T>C | CA375975777 | GATA3 | c.1208T>C (p.Leu403Pro) c.1211T>C (p.Leu404Pro) n.730T>C | gnomAD v4 |
10 | g.8073899T>G | CA375975778 | GATA3 | c.1208T>G (p.Leu403Arg) c.1211T>G (p.Leu404Arg) n.730T>G |