Primary Site >> Stomach Cancer
Gene >> MUC3A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379458 |
| Start | 100960334:100960334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8555C>G |
| AA Mutation | p.Thr2852Ser(p.T2852S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379458 |
| Start | 100960516:100960516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8737T>C |
| AA Mutation | p.Ser2913Pro(p.S2913P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379458 |
| Start | 100960062:100960062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8283T>G |
| AA Mutation | p.Ile2761Met(p.I2761M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379458 |
| Start | 100960189:100960189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8410A>C |
| AA Mutation | p.Thr2804Pro(p.T2804P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379458 |
| Start | 100959407:100959407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7628C>G |
| AA Mutation | p.Thr2543Ser(p.T2543S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379458 |
| Start | 100960896:100960896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762561742 |
| CDS Mutation | c.9011A>G |
| AA Mutation | p.Tyr3004Cys(p.Y3004C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379458 |
| Start | 100959484:100959484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7705A>G |
| AA Mutation | p.Ser2569Gly(p.S2569G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379458 |
| Start | 100959413:100959413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7634C>G |
| AA Mutation | p.Ser2545Cys(p.S2545C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379458 |
| Start | 100958807:100958807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7028C>T |
| AA Mutation | p.Ser2343Phe(p.S2343F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379458 |
| Start | 100960806:100960806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759534118 |
| CDS Mutation | c.8921G>A |
| AA Mutation | p.Gly2974Glu(p.G2974E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379458 |
| Start | 100960930:100960930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9045G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379458 |
| Start | 100960882:100960882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8997C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379458 |
| Start | 100960308:100960308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8529A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379458 |
| Start | 100959534:100959534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573246056 |
| CDS Mutation | c.7755G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379458 |
| Start | 100960449:100960449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373990960 |
| CDS Mutation | c.8670G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379458 |
| Start | 100959273:100959273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7494C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379458 |
| Start | 100963720:100963720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9201C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |