Primary Site >> Stomach Cancer
Gene >> AOC3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308423 |
| Start | 42852121:42852121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.778A>G |
| AA Mutation | p.Thr260Ala(p.T260A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308423 |
| Start | 42854654:42854654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1807T>A |
| AA Mutation | p.Tyr603Asn(p.Y603N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308423 |
| Start | 42852551:42852551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1208A>G |
| AA Mutation | p.Asp403Gly(p.D403G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308423 |
| Start | 42851924:42851924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.581T>C |
| AA Mutation | p.Leu194Pro(p.L194P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308423 |
| Start | 42851959:42851959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764239863 |
| CDS Mutation | c.616C>T |
| AA Mutation | p.Arg206Trp(p.R206W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308423 |
| Start | 42852010:42852010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770810614 |
| CDS Mutation | c.667C>T |
| AA Mutation | p.Arg223Trp(p.R223W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308423 |
| Start | 42856395:42856395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774804718 |
| CDS Mutation | c.2137G>A |
| AA Mutation | p.Glu713Lys(p.E713K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308423 |
| Start | 42852835:42852835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1492G>A |
| AA Mutation | p.Ala498Thr(p.A498T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308423 |
| Start | 42852531:42852531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757676379 |
| CDS Mutation | c.1188G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308423 |
| Start | 42852258:42852258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.915T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308423 |
| Start | 42854572:42854572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146596949 |
| CDS Mutation | c.1725C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308423 |
| Start | 42851853:42851853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs180981981 |
| CDS Mutation | c.510C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000308423 |
| Start | 42852657:42852657(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1318delC |
| AA Mutation | p.Leu440CysfsTer46(p.L440Cfs*46) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000308423 |
| Start | 42851694:42851694(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.356delC |
| AA Mutation | p.Pro119HisfsTer20(p.P119Hfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000308423 |
| Start | 42856484:42856485(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2230dupC |
| AA Mutation | p.Gln744ProfsTer38(p.Q744Pfs*38) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000308423 |
| Start | 42851828:42851829(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.490dupC |
| AA Mutation | p.Leu164ProfsTer92(p.L164Pfs*92) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |