Primary Site >> Stomach Cancer
Gene >> DUOX2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45095444:45095444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766067391 |
| CDS Mutation | c.4232G>A |
| AA Mutation | p.Cys1411Tyr(p.C1411Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45097264:45097264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3821T>C |
| AA Mutation | p.Val1274Ala(p.V1274A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45106568:45106568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1905A>C |
| AA Mutation | p.Lys635Asn(p.K635N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45107417:45107417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140940946 |
| CDS Mutation | c.1621C>T |
| AA Mutation | p.Arg541Trp(p.R541W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45094642:45094642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750546082 |
| CDS Mutation | c.4445C>T |
| AA Mutation | p.Thr1482Met(p.T1482M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45099809:45099809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533557003 |
| CDS Mutation | c.3268G>A |
| AA Mutation | p.Val1090Ile(p.V1090I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45106291:45106291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1982C>T |
| AA Mutation | p.Pro661Leu(p.P661L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45095905:45095905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4003G>A |
| AA Mutation | p.Ala1335Thr(p.A1335T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45108875:45108875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1312C>A |
| AA Mutation | p.Leu438Met(p.L438M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45106207:45106207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2066C>T |
| AA Mutation | p.Pro689Leu(p.P689L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45112572:45112572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148211186 |
| CDS Mutation | c.307G>A |
| AA Mutation | p.Val103Ile(p.V103I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45106219:45106219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2054T>C |
| AA Mutation | p.Val685Ala(p.V685A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45099817:45099817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776772769 |
| CDS Mutation | c.3260C>T |
| AA Mutation | p.Ala1087Val(p.A1087V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45101247:45101247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2879T>C |
| AA Mutation | p.Ile960Thr(p.I960T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45099820:45099820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201362841 |
| CDS Mutation | c.3257C>T |
| AA Mutation | p.Thr1086Met(p.T1086M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45094613:45094613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747720952 |
| CDS Mutation | c.4474C>T |
| AA Mutation | p.Arg1492Cys(p.R1492C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45095908:45095908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200541410 |
| CDS Mutation | c.4000C>T |
| AA Mutation | p.Arg1334Trp(p.R1334W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45095447:45095447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4229T>C |
| AA Mutation | p.Leu1410Pro(p.L1410P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45094654:45094654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759342749 |
| CDS Mutation | c.4433G>A |
| AA Mutation | p.Arg1478Gln(p.R1478Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45112686:45112686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.193T>C |
| AA Mutation | p.Tyr65His(p.Y65H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45099712:45099712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3365C>T |
| AA Mutation | p.Ala1122Val(p.A1122V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000603300 |
| Start | 45112681:45112681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.198C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000603300 |
| Start | 45099828:45099828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3249A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000603300 |
| Start | 45108851:45108851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1336C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000603300 |
| Start | 45112636:45112636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369158930 |
| CDS Mutation | c.243G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000603300 |
| Start | 45095578:45095578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150609056 |
| CDS Mutation | c.4098G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000603300 |
| Start | 45112563:45112563(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.316delG |
| AA Mutation | p.Val106SerfsTer12(p.V106Sfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000603300 |
| Start | 45100788:45100788(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2972delG |
| AA Mutation | p.Gly991GlufsTer5(p.G991Efs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000603300 |
| Start | 45107372:45107372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771710411 |
| CDS Mutation | c.1666C>T |
| AA Mutation | p.Gln556Ter(p.Q556*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |