Primary Site >> Stomach Cancer
Gene >> KSR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398988 |
| Start | 27582921:27582921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747981973 |
| CDS Mutation | c.385C>T |
| AA Mutation | p.His129Tyr(p.H129Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398988 |
| Start | 27611575:27611575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2094C>A |
| AA Mutation | p.Ser698Arg(p.S698R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398988 |
| Start | 27605656:27605656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1492G>A |
| AA Mutation | p.Glu498Lys(p.E498K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398988 |
| Start | 27582691:27582691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.155G>A |
| AA Mutation | p.Arg52Gln(p.R52Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398988 |
| Start | 27609313:27609313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375451001 |
| CDS Mutation | c.1864G>A |
| AA Mutation | p.Val622Met(p.V622M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398988 |
| Start | 27607927:27607927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759272239 |
| CDS Mutation | c.1663C>T |
| AA Mutation | p.Arg555Trp(p.R555W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398988 |
| Start | 27607983:27607983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564032376 |
| CDS Mutation | c.1719G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398988 |
| Start | 27582938:27582938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770956090 |
| CDS Mutation | c.402G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398988 |
| Start | 27605685:27605685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376065082 |
| CDS Mutation | c.1521C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398988 |
| Start | 27583091:27583091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376690107 |
| CDS Mutation | c.555C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000398988 |
| Start | 27597388:27597388(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1014delC |
| AA Mutation | p.Asn339ThrfsTer45(p.N339Tfs*45) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000398988 |
| Start | 27582907:27582907(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.376delC |
| AA Mutation | p.Arg126ValfsTer21(p.R126Vfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |