Primary Site >> Stomach Cancer
Gene >> ANKRD36
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420699 |
| Start | 97200342:97200342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746699789 |
| CDS Mutation | c.2764C>T |
| AA Mutation | p.Arg922Trp(p.R922W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420699 |
| Start | 97245500:97245500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4913G>A |
| AA Mutation | p.Arg1638Gln(p.R1638Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420699 |
| Start | 97196618:97196618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2577G>C |
| AA Mutation | p.Leu859Phe(p.L859F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420699 |
| Start | 97118422:97118422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.391G>A |
| AA Mutation | p.Gly131Arg(p.G131R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420699 |
| Start | 97200358:97200358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372336403 |
| CDS Mutation | c.2780T>C |
| AA Mutation | p.Leu927Ser(p.L927S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420699 |
| Start | 97192985:97192985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2381C>A |
| AA Mutation | p.Thr794Lys(p.T794K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420699 |
| Start | 97245491:97245491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4904A>G |
| AA Mutation | p.Asn1635Ser(p.N1635S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420699 |
| Start | 97118441:97118441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.410A>G |
| AA Mutation | p.Tyr137Cys(p.Y137C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420699 |
| Start | 97118412:97118412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557107594 |
| CDS Mutation | c.381G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000420699 |
| Start | 97243863:97243863(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs762375434 |
| CDS Mutation | c.4409delA |
| AA Mutation | p.Lys1470ArgfsTer17(p.K1470Rfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000420699 |
| Start | 97209842:97209843(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3344dupA |
| AA Mutation | p.Asp1116GlyfsTer6(p.D1116Gfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000420699 |
| Start | 97118473:97118474(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.447dupA |
| AA Mutation | p.Leu150ThrfsTer9(p.L150Tfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |