Primary Site >> Stomach Cancer
Gene >> MUC5AC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1162542:1162542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.484C>T |
| AA Mutation | p.Pro162Ser(p.P162S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1164512:1164512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1109C>A |
| AA Mutation | p.Ala370Asp(p.A370D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1192391:1192391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14246C>A |
| AA Mutation | p.Pro4749His(p.P4749H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1192088:1192088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13943G>T |
| AA Mutation | p.Gly4648Val(p.G4648V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1162113:1162113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.418G>A |
| AA Mutation | p.Val140Met(p.V140M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1193608:1193608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14704G>A |
| AA Mutation | p.Ala4902Thr(p.A4902T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1194163:1194163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14809T>C |
| AA Mutation | p.Tyr4937His(p.Y4937H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1194265:1194265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14911G>A |
| AA Mutation | p.Asp4971Asn(p.D4971N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1162149:1162149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768950562 |
| CDS Mutation | c.454G>A |
| AA Mutation | p.Val152Ile(p.V152I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1165632:1165632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554248382 |
| CDS Mutation | c.1258G>A |
| AA Mutation | p.Gly420Arg(p.G420R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1199902:1199902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763107684 |
| CDS Mutation | c.16633G>A |
| AA Mutation | p.Gly5545Ser(p.G5545S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1163936:1163936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754238142 |
| CDS Mutation | c.734C>T |
| AA Mutation | p.Thr245Met(p.T245M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621226 |
| Start | 1165305:1165305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377067279 |
| CDS Mutation | c.1133C>T |
| AA Mutation | p.Thr378Met(p.T378M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621226 |
| Start | 1162148:1162148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749675435 |
| CDS Mutation | c.453C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621226 |
| Start | 1160634:1160634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79836765 |
| CDS Mutation | c.96C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621226 |
| Start | 1165712:1165712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775592062 |
| CDS Mutation | c.1338C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621226 |
| Start | 1195208:1195208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15387T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621226 |
| Start | 1165369:1165369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554285235 |
| CDS Mutation | c.1197C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621226 |
| Start | 1200573:1200573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775257388 |
| CDS Mutation | c.16836C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621226 |
| Start | 1194231:1194231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528299547 |
| CDS Mutation | c.14877C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000621226 |
| Start | 1195903:1195903(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.15491delC |
| AA Mutation | p.Pro5164HisfsTer15(p.P5164Hfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000621226 |
| Start | 1164280:1164280(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.969delG |
| AA Mutation | p.Leu324CysfsTer137(p.L324Cfs*137) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |