Primary Site >> Stomach Cancer
Gene >> PIK3C2B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204460331:204460331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1495A>C |
| AA Mutation | p.Ile499Leu(p.I499L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204431693:204431693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4256T>G |
| AA Mutation | p.Leu1419Arg(p.L1419R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204449190:204449190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2341C>A |
| AA Mutation | p.Leu781Met(p.L781M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204469141:204469141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753876041 |
| CDS Mutation | c.662G>A |
| AA Mutation | p.Arg221His(p.R221H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204434445:204434445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3680T>C |
| AA Mutation | p.Ile1227Thr(p.I1227T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204449947:204449947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2137C>T |
| AA Mutation | p.Pro713Ser(p.P713S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204446056:204446056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751159224 |
| CDS Mutation | c.2578G>A |
| AA Mutation | p.Ala860Thr(p.A860T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204432363:204432363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3992T>C |
| AA Mutation | p.Leu1331Pro(p.L1331P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204432234:204432234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776940848 |
| CDS Mutation | c.4121G>A |
| AA Mutation | p.Arg1374His(p.R1374H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204444401:204444401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375521608 |
| CDS Mutation | c.2702G>A |
| AA Mutation | p.Arg901His(p.R901H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204424871:204424871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770075841 |
| CDS Mutation | c.4886G>A |
| AA Mutation | p.Arg1629Gln(p.R1629Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204432324:204432324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139230011 |
| CDS Mutation | c.4031C>T |
| AA Mutation | p.Thr1344Met(p.T1344M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204446098:204446098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2536T>C |
| AA Mutation | p.Cys846Arg(p.C846R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204469150:204469150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.653G>C |
| AA Mutation | p.Gly218Ala(p.G218A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204443575:204443575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2890G>A |
| AA Mutation | p.Asp964Asn(p.D964N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204464073:204464073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1249A>G |
| AA Mutation | p.Arg417Gly(p.R417G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204429934:204429934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4385C>T |
| AA Mutation | p.Pro1462Leu(p.P1462L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204469637:204469637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166T>C |
| AA Mutation | p.Ser56Pro(p.S56P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204455865:204455865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1934G>C |
| AA Mutation | p.Trp645Ser(p.W645S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367187 |
| Start | 204449205:204449205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2326C>T |
| AA Mutation | p.Pro776Ser(p.P776S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367187 |
| Start | 204469191:204469191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.612G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367187 |
| Start | 204443543:204443543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2922G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367187 |
| Start | 204469077:204469077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146926130 |
| CDS Mutation | c.726G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367187 |
| Start | 204469688:204469688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.115C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367187 |
| Start | 204468944:204468944(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.859delC |
| AA Mutation | p.Arg287AlafsTer92(p.R287Afs*92) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367187 |
| Start | 204447531:204447532(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs760150806 |
| CDS Mutation | c.2393dupC |
| AA Mutation | p.Gly799TrpfsTer9(p.G799Wfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |