Primary Site >> Stomach Cancer
Gene >> EPHB6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142868552:142868552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2099T>C |
| AA Mutation | p.Val700Ala(p.V700A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142870224:142870224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140748660 |
| CDS Mutation | c.2621C>A |
| AA Mutation | p.Ala874Glu(p.A874E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142864134:142864134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548632943 |
| CDS Mutation | c.334C>T |
| AA Mutation | p.Arg112Trp(p.R112W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142870673:142870673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2948A>G |
| AA Mutation | p.Gln983Arg(p.Q983R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142866535:142866535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747288408 |
| CDS Mutation | c.1517C>T |
| AA Mutation | p.Thr506Met(p.T506M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142868293:142868293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1971G>T |
| AA Mutation | p.Gln657His(p.Q657H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142870347:142870347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2744C>A |
| AA Mutation | p.Ala915Glu(p.A915E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142868244:142868244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1922T>C |
| AA Mutation | p.Leu641Pro(p.L641P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142864108:142864108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756659047 |
| CDS Mutation | c.308C>T |
| AA Mutation | p.Ala103Val(p.A103V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142868271:142868271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143338098 |
| CDS Mutation | c.1949C>T |
| AA Mutation | p.Ser650Phe(p.S650F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142864125:142864125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.325T>G |
| AA Mutation | p.Phe109Val(p.F109V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142868581:142868581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752688738 |
| CDS Mutation | c.2128G>A |
| AA Mutation | p.Ala710Thr(p.A710T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142866493:142866493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1475T>C |
| AA Mutation | p.Val492Ala(p.V492A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619012 |
| Start | 142864095:142864095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375010348 |
| CDS Mutation | c.295G>A |
| AA Mutation | p.Gly99Arg(p.G99R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619012 |
| Start | 142869846:142869846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2490C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619012 |
| Start | 142864217:142864217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.417C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619012 |
| Start | 142864400:142864400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.600G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000619012 |
| Start | 142864643:142864643(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.849delC |
| AA Mutation | p.Arg284GlyfsTer12(p.R284Gfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000619012 |
| Start | 142868593:142868593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2140C>T |
| AA Mutation | p.Gln714Ter(p.Q714*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |