Primary Site >> Stomach Cancer
Gene >> INTS8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000523731 |
| Start | 94824898:94824898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749115981 |
| CDS Mutation | c.136G>A |
| AA Mutation | p.Ala46Thr(p.A46T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000523731 |
| Start | 94876120:94876120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752848840 |
| CDS Mutation | c.2735C>T |
| AA Mutation | p.Ala912Val(p.A912V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000523731 |
| Start | 94824944:94824944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.182C>A |
| AA Mutation | p.Pro61His(p.P61H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000523731 |
| Start | 94836602:94836602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.832T>A |
| AA Mutation | p.Phe278Ile(p.F278I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000523731 |
| Start | 94827394:94827394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.437A>G |
| AA Mutation | p.Tyr146Cys(p.Y146C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000523731 |
| Start | 94849994:94849994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1410A>T |
| AA Mutation | p.Lys470Asn(p.K470N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000523731 |
| Start | 94876126:94876126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2741A>C |
| AA Mutation | p.Lys914Thr(p.K914T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000523731 |
| Start | 94880130:94880130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2884G>A |
| AA Mutation | p.Gly962Ser(p.G962S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000523731 |
| Start | 94880226:94880226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2980T>C |
| AA Mutation | p.Tyr994His(p.Y994H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000523731 |
| Start | 94880189:94880189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2943A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000523731 |
| Start | 94851644:94851644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1599T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000523731 |
| Start | 94832069:94832069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.648G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000523731 |
| Start | 94856819:94856819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1795T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000523731 |
| Start | 94836602:94836602(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.837delT |
| AA Mutation | p.Phe279LeufsTer6(p.F279Lfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000523731 |
| Start | 94880193:94880193(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2954delA |
| AA Mutation | p.Lys985SerfsTer44(p.K985Sfs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000523731 |
| Start | 94865626:94865626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2197C>T |
| AA Mutation | p.Arg733Ter(p.R733*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000523731 |
| Start | 94874561:94874561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755100105 |
| CDS Mutation | c.2647C>T |
| AA Mutation | p.Arg883Ter(p.R883*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000523731 |
| Start | 94853823:94853824(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1662_1696dupTAGTGGTGTTATCCTGGGAATTAAAGACAATTTAA |
| AA Mutation | p.Thr566IlefsTer12(p.T566Ifs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000523731 |
| Start | 94841503:94841504(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1034dupT |
| AA Mutation | p.Ile346HisfsTer2(p.I346Hfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000523731 |
| Start | 94853872:94853880(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1711_1719delTATATTCTT |
| AA Mutation | p.Tyr571_Leu573del(p.Y571_L573del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |