Primary Site >> Stomach Cancer
Gene >> F10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375559 |
| Start | 113129461:113129461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.80G>A |
| AA Mutation | p.Arg27His(p.R27H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375559 |
| Start | 113148945:113148945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745764165 |
| CDS Mutation | c.895G>A |
| AA Mutation | p.Gly299Ser(p.G299S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375559 |
| Start | 113129584:113129584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776339896 |
| CDS Mutation | c.203G>A |
| AA Mutation | p.Arg68His(p.R68H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375559 |
| Start | 113139449:113139449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.349G>A |
| AA Mutation | p.Glu117Lys(p.E117K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375559 |
| Start | 113149085:113149085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1035G>T |
| AA Mutation | p.Glu345Asp(p.E345D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375559 |
| Start | 113149066:113149066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201675411 |
| CDS Mutation | c.1016C>T |
| AA Mutation | p.Ala339Val(p.A339V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375559 |
| Start | 113149097:113149097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545046199 |
| CDS Mutation | c.1047C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375559 |
| Start | 113129573:113129573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.192C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375559 |
| Start | 113129585:113129585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376704564 |
| CDS Mutation | c.204C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375559 |
| Start | 113141016:113141016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.468C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375559 |
| Start | 113149346:113149346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139031355 |
| CDS Mutation | c.1296C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375559 |
| Start | 113147398:113147398(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.770delA |
| AA Mutation | p.Asn257ThrfsTer10(p.N257Tfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |