Primary Site >> Stomach Cancer
Gene >> KIF20A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394894 |
| Start | 138179766:138179766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.86C>T |
| AA Mutation | p.Ala29Val(p.A29V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394894 |
| Start | 138184635:138184635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1642G>A |
| AA Mutation | p.Asp548Asn(p.D548N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000394894 |
| Start | 138184104:138184104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1351C>T |
| AA Mutation | p.Arg451Trp(p.R451W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394894 |
| Start | 138187370:138187370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754343932 |
| CDS Mutation | c.2630G>A |
| AA Mutation | p.Arg877His(p.R877H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394894 |
| Start | 138183273:138183273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.937C>A |
| AA Mutation | p.Leu313Ile(p.L313I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394894 |
| Start | 138187204:138187204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2464G>T |
| AA Mutation | p.Gly822Cys(p.G822C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394894 |
| Start | 138183229:138183229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144155991 |
| CDS Mutation | c.893G>A |
| AA Mutation | p.Arg298His(p.R298H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394894 |
| Start | 138183292:138183292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375379655 |
| CDS Mutation | c.956C>T |
| AA Mutation | p.Pro319Leu(p.P319L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394894 |
| Start | 138185640:138185640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2055C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394894 |
| Start | 138186049:138186049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2214G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394894 |
| Start | 138187357:138187357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2617C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394894 |
| Start | 138183724:138183724(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1180delG |
| AA Mutation | p.Glu394LysfsTer4(p.E394Kfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000394894 |
| Start | 138184035:138184035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1282G>T |
| AA Mutation | p.Gly428Ter(p.G428*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000394894 |
| Start | 138183180:138183180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777958054 |
| CDS Mutation | c.844C>T |
| AA Mutation | p.Arg282Ter(p.R282*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000394894 |
| Start | 138179744:138179745(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.64_65insA |
| AA Mutation | p.Pro22HisfsTer4(p.P22Hfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |