Primary Site >> Stomach Cancer
Gene >> DUOX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45152012:45152012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3153C>A |
| AA Mutation | p.Phe1051Leu(p.F1051L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45161891:45161891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779696519 |
| CDS Mutation | c.4010G>A |
| AA Mutation | p.Arg1337Gln(p.R1337Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45152409:45152409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3317G>A |
| AA Mutation | p.Arg1106His(p.R1106H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45141043:45141043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748345295 |
| CDS Mutation | c.1538G>A |
| AA Mutation | p.Arg513His(p.R513H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45135919:45135919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.835G>A |
| AA Mutation | p.Ala279Thr(p.A279T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45141030:45141030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757808802 |
| CDS Mutation | c.1525C>T |
| AA Mutation | p.Arg509Trp(p.R509W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45136615:45136615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767305748 |
| CDS Mutation | c.1012G>A |
| AA Mutation | p.Val338Ile(p.V338I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45155850:45155850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3623T>G |
| AA Mutation | p.Phe1208Cys(p.F1208C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45152471:45152471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3379G>A |
| AA Mutation | p.Val1127Met(p.V1127M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45147643:45147643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2533G>T |
| AA Mutation | p.Val845Leu(p.V845L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45141006:45141006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149290661 |
| CDS Mutation | c.1501G>A |
| AA Mutation | p.Val501Ile(p.V501I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45163827:45163827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186783799 |
| CDS Mutation | c.4442G>A |
| AA Mutation | p.Arg1481Gln(p.R1481Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45150668:45150668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2855G>A |
| AA Mutation | p.Arg952Gln(p.R952Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45152007:45152007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3148G>A |
| AA Mutation | p.Val1050Met(p.V1050M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45136537:45136537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147597074 |
| CDS Mutation | c.934C>T |
| AA Mutation | p.Pro312Ser(p.P312S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45144135:45144135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2036G>A |
| AA Mutation | p.Arg679His(p.R679H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45152506:45152506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3414C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45160920:45160920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766484602 |
| CDS Mutation | c.3786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45140999:45140999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1494C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45136569:45136569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.966C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45151190:45151190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2956C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45148431:45148431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2802G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45153396:45153396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3441C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45151192:45151192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2958G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45135238:45135238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.442A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45139071:45139071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1119A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45153438:45153438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3483C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45136536:45136536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.933G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45148425:45148425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2796C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321429 |
| Start | 45147916:45147916(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2564delA |
| AA Mutation | p.Lys855SerfsTer26(p.K855Sfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321429 |
| Start | 45163622:45163623(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.4340_4343dupTGGT |
| AA Mutation | p.Ser1449GlyfsTer12(p.S1449Gfs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321429 |
| Start | 45147978:45147979(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2624_2627dupAGTT |
| AA Mutation | p.Phe876LeufsTer24(p.F876Lfs*24) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000321429 |
| Start | 45151872:45151872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771158337 |
| CDS Mutation | c.3015-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |