| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.26779249del | CA16617134 | ARID1A | c.5351del (p.Asn1784MetfsTer5) c.4202del (p.Asn1401MetfsTer5) c.4199del (p.Asn1400MetfsTer5) c.768del c.4205del (p.Asn1402MetfsTer5) n.1151del c.2040del c.4700del (p.Asn1567MetfsTer5) c.849del | ClinVar dbSNP |
| 1 | g.26779249_26779262del | CA645513195 | ARID1A | c.5351_5364del (p.Asn1784SerfsTer13) c.4202_4215del (p.Asn1401SerfsTer13) c.4199_4212del (p.Asn1400SerfsTer13) c.768_781del c.4205_4218del (p.Asn1402SerfsTer13) n.1151_1164del c.2040_2053del c.4700_4713del (p.Asn1567SerfsTer13) c.849_862del | COSMIC |
| 1 | g.26779249A>C | CA339184909 | ARID1A | c.5351A>C (p.Asn1784Thr) c.4202A>C (p.Asn1401Thr) c.4199A>C (p.Asn1400Thr) c.768A>C c.4205A>C (p.Asn1402Thr) n.1151A>C c.2040A>C c.4700A>C (p.Asn1567Thr) c.849A>C | |
| 1 | g.26779249A>G | CA339184910 | ARID1A | c.5351A>G (p.Asn1784Ser) c.4202A>G (p.Asn1401Ser) c.4199A>G (p.Asn1400Ser) c.768A>G c.4205A>G (p.Asn1402Ser) n.1151A>G c.2040A>G c.4700A>G (p.Asn1567Ser) c.849A>G | dbSNP COSMIC |
| 1 | g.26779249A>T | CA339184911 | ARID1A | c.5351A>T (p.Asn1784Ile) c.4202A>T (p.Asn1401Ile) c.4199A>T (p.Asn1400Ile) c.768A>T c.4205A>T (p.Asn1402Ile) n.1151A>T c.2040A>T c.4700A>T (p.Asn1567Ile) c.849A>T | dbSNP |
| 1 | g.26779253_26779255del | CA2644301425 | ARID1A | c.5355_5357del (p.Asp1785del) c.4206_4208del (p.Asp1402del) c.4203_4205del (p.Asp1401del) c.772_774del c.4209_4211del (p.Asp1403del) n.1155_1157del c.2044_2046del c.4704_4706del (p.Asp1568del) c.853_855del | gnomAD v4 |
| 1 | g.26779250T>A | CA339184913 | ARID1A | c.5352T>A (p.Asn1784Lys) c.4203T>A (p.Asn1401Lys) c.4200T>A (p.Asn1400Lys) c.769T>A c.4206T>A (p.Asn1402Lys) n.1152T>A c.2041T>A c.4701T>A (p.Asn1567Lys) c.850T>A | dbSNP |
| 1 | g.26779250T>C | CA416968258 | ARID1A | c.5352T>C (p.Asn1784=) c.4203T>C (p.Asn1401=) c.4200T>C (p.Asn1400=) c.769T>C c.4206T>C (p.Asn1402=) n.1152T>C c.2041T>C c.4701T>C (p.Asn1567=) c.850T>C | |
| 1 | g.26779250T>G | CA339184915 | ARID1A | c.5352T>G (p.Asn1784Lys) c.4203T>G (p.Asn1401Lys) c.4200T>G (p.Asn1400Lys) c.769T>G c.4206T>G (p.Asn1402Lys) n.1152T>G c.2041T>G c.4701T>G (p.Asn1567Lys) c.850T>G | dbSNP |
| 1 | g.26779251G>A | CA339184918 | ARID1A | c.5353G>A (p.Asp1785Asn) c.4204G>A (p.Asp1402Asn) c.4201G>A (p.Asp1401Asn) c.770G>A c.4207G>A (p.Asp1403Asn) n.1153G>A c.2042G>A c.4702G>A (p.Asp1568Asn) c.851G>A | dbSNP |
| 1 | g.26779251G>C | CA339184919 | ARID1A | c.5353G>C (p.Asp1785His) c.4204G>C (p.Asp1402His) c.4201G>C (p.Asp1401His) c.770G>C c.4207G>C (p.Asp1403His) n.1153G>C c.2042G>C c.4702G>C (p.Asp1568His) c.851G>C | dbSNP |
| 1 | g.26779251G>T | CA339184921 | ARID1A | c.5353G>T (p.Asp1785Tyr) c.4204G>T (p.Asp1402Tyr) c.4201G>T (p.Asp1401Tyr) c.770G>T c.4207G>T (p.Asp1403Tyr) n.1153G>T c.2042G>T c.4702G>T (p.Asp1568Tyr) c.851G>T | dbSNP |
| 1 | g.26779252A= | CA1160218045 | ARID1A | c.5354A= (p.Asp1785=) c.4205A= (p.Asp1402=) c.4202A= (p.Asp1401=) c.771A= c.4208A= (p.Asp1403=) n.1154A= c.2043A= c.4703A= (p.Asp1568=) c.852A= | |
| 1 | g.26779252A>C | CA339184928 | ARID1A | c.5354A>C (p.Asp1785Ala) c.4205A>C (p.Asp1402Ala) c.4202A>C (p.Asp1401Ala) c.771A>C c.4208A>C (p.Asp1403Ala) n.1154A>C c.2043A>C c.4703A>C (p.Asp1568Ala) c.852A>C | dbSNP |
| 1 | g.26779252A>G | CA339184926 | ARID1A | c.5354A>G (p.Asp1785Gly) c.4205A>G (p.Asp1402Gly) c.4202A>G (p.Asp1401Gly) c.771A>G c.4208A>G (p.Asp1403Gly) n.1154A>G c.2043A>G c.4703A>G (p.Asp1568Gly) c.852A>G | dbSNP |
| 1 | g.26779252A>T | CA339184924 | ARID1A | c.5354A>T (p.Asp1785Val) c.4205A>T (p.Asp1402Val) c.4202A>T (p.Asp1401Val) c.771A>T c.4208A>T (p.Asp1403Val) n.1154A>T c.2043A>T c.4703A>T (p.Asp1568Val) c.852A>T | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.26779253T>A | CA339184930 | ARID1A | c.5355T>A (p.Asp1785Glu) c.4206T>A (p.Asp1402Glu) c.4203T>A (p.Asp1401Glu) c.772T>A c.4209T>A (p.Asp1403Glu) n.1155T>A c.2044T>A c.4704T>A (p.Asp1568Glu) c.853T>A | dbSNP gnomAD v4 |
| 1 | g.26779253T>C | CA416968270 | ARID1A | c.5355T>C (p.Asp1785=) c.4206T>C (p.Asp1402=) c.4203T>C (p.Asp1401=) c.772T>C c.4209T>C (p.Asp1403=) n.1155T>C c.2044T>C c.4704T>C (p.Asp1568=) c.853T>C | dbSNP |
| 1 | g.26779253T>G | CA339184931 | ARID1A | c.5355T>G (p.Asp1785Glu) c.4206T>G (p.Asp1402Glu) c.4203T>G (p.Asp1401Glu) c.772T>G c.4209T>G (p.Asp1403Glu) n.1155T>G c.2044T>G c.4704T>G (p.Asp1568Glu) c.853T>G | dbSNP |
| 1 | g.26779253T= | CA1160218046 | ARID1A | c.5355T= (p.Asp1785=) c.4206T= (p.Asp1402=) c.4203T= (p.Asp1401=) c.772T= c.4209T= (p.Asp1403=) n.1155T= c.2044T= c.4704T= (p.Asp1568=) c.853T= | |
| 1 | g.26779254G>A | CA339184934 | ARID1A | c.5356G>A (p.Glu1786Lys) c.4207G>A (p.Glu1403Lys) c.4204G>A (p.Glu1402Lys) c.773G>A c.4210G>A (p.Glu1404Lys) n.1156G>A c.2045G>A c.4705G>A (p.Glu1569Lys) c.854G>A | dbSNP |
| 1 | g.26779254G>C | CA339184936 | ARID1A | c.5356G>C (p.Glu1786Gln) c.4207G>C (p.Glu1403Gln) c.4204G>C (p.Glu1402Gln) c.773G>C c.4210G>C (p.Glu1404Gln) n.1156G>C c.2045G>C c.4705G>C (p.Glu1569Gln) c.854G>C | dbSNP |
| 1 | g.26779254G= | CA1160218047 | ARID1A | c.5356G= (p.Glu1786=) c.4207G= (p.Glu1403=) c.4204G= (p.Glu1402=) c.773G= c.4210G= (p.Glu1404=) n.1156G= c.2045G= c.4705G= (p.Glu1569=) c.854G= | |
| 1 | g.26779254G>T | CA339184939 | ARID1A | c.5356G>T (p.Glu1786Ter) c.4207G>T (p.Glu1403Ter) c.4204G>T (p.Glu1402Ter) c.773G>T c.4210G>T (p.Glu1404Ter) n.1156G>T c.2045G>T c.4705G>T (p.Glu1569Ter) c.854G>T | dbSNP |
| 1 | g.26779257_26779259del | CA2644301426 | ARID1A | c.5359_5361del (p.Glu1787del) c.4210_4212del (p.Glu1404del) c.4207_4209del (p.Glu1403del) c.776_778del c.4213_4215del (p.Glu1405del) n.1159_1161del c.2048_2050del c.4708_4710del (p.Glu1570del) c.857_859del | gnomAD v4 |
| 1 | g.26779255A>C | CA339184942 | ARID1A | c.5357A>C (p.Glu1786Ala) c.4208A>C (p.Glu1403Ala) c.4205A>C (p.Glu1402Ala) c.774A>C c.4211A>C (p.Glu1404Ala) n.1157A>C c.2046A>C c.4706A>C (p.Glu1569Ala) c.855A>C | |
| 1 | g.26779255A>G | CA339184943 | ARID1A | c.5357A>G (p.Glu1786Gly) c.4208A>G (p.Glu1403Gly) c.4205A>G (p.Glu1402Gly) c.774A>G c.4211A>G (p.Glu1404Gly) n.1157A>G c.2046A>G c.4706A>G (p.Glu1569Gly) c.855A>G | dbSNP |
| 1 | g.26779255A>T | CA339184945 | ARID1A | c.5357A>T (p.Glu1786Val) c.4208A>T (p.Glu1403Val) c.4205A>T (p.Glu1402Val) c.774A>T c.4211A>T (p.Glu1404Val) n.1157A>T c.2046A>T c.4706A>T (p.Glu1569Val) c.855A>T | dbSNP |
| 1 | g.26779256G>A | CA19815265 | ARID1A | c.5358G>A (p.Glu1786=) c.4209G>A (p.Glu1403=) c.4206G>A (p.Glu1402=) c.775G>A c.4212G>A (p.Glu1404=) n.1158G>A c.2047G>A c.4707G>A (p.Glu1569=) c.856G>A | dbSNP gnomAD v4 |
| 1 | g.26779256G>C | CA339184948 | ARID1A | c.5358G>C (p.Glu1786Asp) c.4209G>C (p.Glu1403Asp) c.4206G>C (p.Glu1402Asp) c.775G>C c.4212G>C (p.Glu1404Asp) n.1158G>C c.2047G>C c.4707G>C (p.Glu1569Asp) c.856G>C | dbSNP |
| 1 | g.26779256G= | CA1160218048 | ARID1A | c.5358G= (p.Glu1786=) c.4209G= (p.Glu1403=) c.4206G= (p.Glu1402=) c.775G= c.4212G= (p.Glu1404=) n.1158G= c.2047G= c.4707G= (p.Glu1569=) c.856G= | |
| 1 | g.26779256G>T | CA339184950 | ARID1A | c.5358G>T (p.Glu1786Asp) c.4209G>T (p.Glu1403Asp) c.4206G>T (p.Glu1402Asp) c.775G>T c.4212G>T (p.Glu1404Asp) n.1158G>T c.2047G>T c.4707G>T (p.Glu1569Asp) c.856G>T | dbSNP |
| 1 | g.26779257G>A | CA339184953 | ARID1A | c.5359G>A (p.Glu1787Lys) c.4210G>A (p.Glu1404Lys) c.4207G>A (p.Glu1403Lys) c.776G>A c.4213G>A (p.Glu1405Lys) n.1159G>A c.2048G>A c.4708G>A (p.Glu1570Lys) c.857G>A | dbSNP gnomAD v2 |
| 1 | g.26779257G>C | CA339184954 | ARID1A | c.5359G>C (p.Glu1787Gln) c.4210G>C (p.Glu1404Gln) c.4207G>C (p.Glu1403Gln) c.776G>C c.4213G>C (p.Glu1405Gln) n.1159G>C c.2048G>C c.4708G>C (p.Glu1570Gln) c.857G>C | dbSNP |
| 1 | g.26779257G= | CA1160218049 | ARID1A | c.5359G= (p.Glu1787=) c.4210G= (p.Glu1404=) c.4207G= (p.Glu1403=) c.776G= c.4213G= (p.Glu1405=) n.1159G= c.2048G= c.4708G= (p.Glu1570=) c.857G= | |
| 1 | g.26779257G>T | CA339184957 | ARID1A | c.5359G>T (p.Glu1787Ter) c.4210G>T (p.Glu1404Ter) c.4207G>T (p.Glu1403Ter) c.776G>T c.4213G>T (p.Glu1405Ter) n.1159G>T c.2048G>T c.4708G>T (p.Glu1570Ter) c.857G>T | dbSNP COSMIC |
| 1 | g.26779258A>C | CA339184963 | ARID1A | c.5360A>C (p.Glu1787Ala) c.4211A>C (p.Glu1404Ala) c.4208A>C (p.Glu1403Ala) c.777A>C c.4214A>C (p.Glu1405Ala) n.1160A>C c.2049A>C c.4709A>C (p.Glu1570Ala) c.858A>C | |
| 1 | g.26779258A>G | CA339184961 | ARID1A | c.5360A>G (p.Glu1787Gly) c.4211A>G (p.Glu1404Gly) c.4208A>G (p.Glu1403Gly) c.777A>G c.4214A>G (p.Glu1405Gly) n.1160A>G c.2049A>G c.4709A>G (p.Glu1570Gly) c.858A>G | |
| 1 | g.26779258A>T | CA339184960 | ARID1A | c.5360A>T (p.Glu1787Val) c.4211A>T (p.Glu1404Val) c.4208A>T (p.Glu1403Val) c.777A>T c.4214A>T (p.Glu1405Val) n.1160A>T c.2049A>T c.4709A>T (p.Glu1570Val) c.858A>T | dbSNP |
| 1 | g.26779260_26779263dup | CA645513197 | ARID1A | c.5362_5365dup (p.Ala1789AspfsTer14) c.4213_4216dup (p.Ala1406AspfsTer14) c.4210_4213dup (p.Ala1405AspfsTer14) c.779_782dup c.4216_4219dup (p.Ala1407AspfsTer14) n.1162_1165dup c.2051_2054dup c.4711_4714dup (p.Ala1572AspfsTer14) c.860_863dup | COSMIC |
| 1 | g.26779259G>A | CA416968288 | ARID1A | c.5361G>A (p.Glu1787=) c.4212G>A (p.Glu1404=) c.4209G>A (p.Glu1403=) c.778G>A c.4215G>A (p.Glu1405=) n.1161G>A c.2050G>A c.4710G>A (p.Glu1570=) c.859G>A | dbSNP |
| 1 | g.26779259G>C | CA339184968 | ARID1A | c.5361G>C (p.Glu1787Asp) c.4212G>C (p.Glu1404Asp) c.4209G>C (p.Glu1403Asp) c.778G>C c.4215G>C (p.Glu1405Asp) n.1161G>C c.2050G>C c.4710G>C (p.Glu1570Asp) c.859G>C | dbSNP |
| 1 | g.26779259G>T | CA339184966 | ARID1A | c.5361G>T (p.Glu1787Asp) c.4212G>T (p.Glu1404Asp) c.4209G>T (p.Glu1403Asp) c.778G>T c.4215G>T (p.Glu1405Asp) n.1161G>T c.2050G>T c.4710G>T (p.Glu1570Asp) c.859G>T | dbSNP |
| 1 | g.26779260A= | CA1160218050 | ARID1A | c.5362A= (p.Ile1788=) c.4213A= (p.Ile1405=) c.4210A= (p.Ile1404=) c.779A= c.4216A= (p.Ile1406=) n.1162A= c.2051A= c.4711A= (p.Ile1571=) c.860A= | |
| 1 | g.26779260A>C | CA339184975 | ARID1A | c.5362A>C (p.Ile1788Leu) c.4213A>C (p.Ile1405Leu) c.4210A>C (p.Ile1404Leu) c.779A>C c.4216A>C (p.Ile1406Leu) n.1162A>C c.2051A>C c.4711A>C (p.Ile1571Leu) c.860A>C | dbSNP |
| 1 | g.26779260A>G | CA707678 | ARID1A | c.5362A>G (p.Ile1788Val) c.4213A>G (p.Ile1405Val) c.4210A>G (p.Ile1404Val) c.779A>G c.4216A>G (p.Ile1406Val) n.1162A>G c.2051A>G c.4711A>G (p.Ile1571Val) c.860A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.26779260A>T | CA339184973 | ARID1A | c.5362A>T (p.Ile1788Leu) c.4213A>T (p.Ile1405Leu) c.4210A>T (p.Ile1404Leu) c.779A>T c.4216A>T (p.Ile1406Leu) n.1162A>T c.2051A>T c.4711A>T (p.Ile1571Leu) c.860A>T | dbSNP |
| 1 | g.26779261T>A | CA339184977 | ARID1A | c.5363T>A (p.Ile1788Lys) c.4214T>A (p.Ile1405Lys) c.4211T>A (p.Ile1404Lys) c.780T>A c.4217T>A (p.Ile1406Lys) n.1163T>A c.2052T>A c.4712T>A (p.Ile1571Lys) c.861T>A | dbSNP |
| 1 | g.26779261T>C | CA339184979 | ARID1A | c.5363T>C (p.Ile1788Thr) c.4214T>C (p.Ile1405Thr) c.4211T>C (p.Ile1404Thr) c.780T>C c.4217T>C (p.Ile1406Thr) n.1163T>C c.2052T>C c.4712T>C (p.Ile1571Thr) c.861T>C | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.26779261T>G | CA339184981 | ARID1A | c.5363T>G (p.Ile1788Arg) c.4214T>G (p.Ile1405Arg) c.4211T>G (p.Ile1404Arg) c.780T>G c.4217T>G (p.Ile1406Arg) n.1163T>G c.2052T>G c.4712T>G (p.Ile1571Arg) c.861T>G | dbSNP |