Primary Site >> Stomach Cancer
Gene >> EPHB3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184579588:184579588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1913T>C |
| AA Mutation | p.Val638Ala(p.V638A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184581063:184581063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779302587 |
| CDS Mutation | c.2630G>A |
| AA Mutation | p.Arg877Gln(p.R877Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184581155:184581155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765545961 |
| CDS Mutation | c.2722G>A |
| AA Mutation | p.Ala908Thr(p.A908T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184580502:184580502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2273A>G |
| AA Mutation | p.Asp758Gly(p.D758G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184581603:184581603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200546160 |
| CDS Mutation | c.2978C>T |
| AA Mutation | p.Thr993Met(p.T993M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184579791:184579791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376071253 |
| CDS Mutation | c.2029C>T |
| AA Mutation | p.Arg677Trp(p.R677W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184576902:184576902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1073A>C |
| AA Mutation | p.Glu358Ala(p.E358A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184579887:184579887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2125A>C |
| AA Mutation | p.Ile709Leu(p.I709L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184572978:184572978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.658G>A |
| AA Mutation | p.Ala220Thr(p.A220T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184577441:184577441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1453G>T |
| AA Mutation | p.Asp485Tyr(p.D485Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184577800:184577800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1622A>G |
| AA Mutation | p.Glu541Gly(p.E541G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330394 |
| Start | 184572661:184572661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.341G>A |
| AA Mutation | p.Arg114His(p.R114H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330394 |
| Start | 184581358:184581358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776581417 |
| CDS Mutation | c.2838C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330394 |
| Start | 184572776:184572776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.456C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330394 |
| Start | 184572911:184572911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.591C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330394 |
| Start | 184579562:184579562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776325182 |
| CDS Mutation | c.1887C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000330394 |
| Start | 184577929:184577930(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1675dupC |
| AA Mutation | p.Leu559ProfsTer32(p.L559Pfs*32) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |