Primary Site >> Stomach Cancer
Gene >> ANKRD12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9254360:9254360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1093G>T |
| AA Mutation | p.Asp365Tyr(p.D365Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9256668:9256668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3401A>G |
| AA Mutation | p.Lys1134Arg(p.K1134R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9257794:9257794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143090707 |
| CDS Mutation | c.4527G>A |
| AA Mutation | p.Met1509Ile(p.M1509I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9258383:9258383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5116G>A |
| AA Mutation | p.Glu1706Lys(p.E1706K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9275605:9275605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5845C>T |
| AA Mutation | p.Pro1949Ser(p.P1949S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9211715:9211715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.583C>G |
| AA Mutation | p.Arg195Gly(p.R195G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9280975:9280975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6038C>T |
| AA Mutation | p.Ala2013Val(p.A2013V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9258424:9258424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5157A>C |
| AA Mutation | p.Glu1719Asp(p.E1719D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9258530:9258530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5263A>G |
| AA Mutation | p.Thr1755Ala(p.T1755A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9257342:9257342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4075C>T |
| AA Mutation | p.Leu1359Phe(p.L1359F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9256589:9256589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3322G>A |
| AA Mutation | p.Glu1108Lys(p.E1108K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9258245:9258245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765291091 |
| CDS Mutation | c.4978C>T |
| AA Mutation | p.Pro1660Ser(p.P1660S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262126 |
| Start | 9221913:9221913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.857G>A |
| AA Mutation | p.Arg286His(p.R286H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262126 |
| Start | 9255016:9255016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1749T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262126 |
| Start | 9211678:9211678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.546T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262126 |
| Start | 9204528:9204528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.288T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262126 |
| Start | 9256064:9256064(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2804delA |
| AA Mutation | p.Asn935IlefsTer24(p.N935Ifs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262126 |
| Start | 9256209:9256209(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2949delA |
| AA Mutation | p.Lys983AsnfsTer4(p.K983Nfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000262126 |
| Start | 9254423:9254423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1156C>T |
| AA Mutation | p.Arg386Ter(p.R386*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262126 |
| Start | 9255187:9255188(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1927dupA |
| AA Mutation | p.Met643AsnfsTer3(p.M643Nfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262126 |
| Start | 9256552:9256553(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3291dupA |
| AA Mutation | p.His1098ThrfsTer2(p.H1098Tfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262126 |
| Start | 9254820:9254821(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1557dupG |
| AA Mutation | p.Asn520GlufsTer3(p.N520Efs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000262126 |
| Start | 9263861:9263863(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5738_5740delTAC |
| AA Mutation | p.Leu1913del(p.L1913del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000262126 |
| Start | 9257031:9257033(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs757311943 |
| CDS Mutation | c.3766_3768delCCT |
| AA Mutation | p.Pro1256del(p.P1256del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000262126 |
| Start | 9221976:9221977(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.930_932dupTGA |
| AA Mutation | p.Asp310dup(p.D310dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |