Primary Site >> Stomach Cancer
Gene >> EPHB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22909143:22909143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758794865 |
| CDS Mutation | c.2474G>A |
| AA Mutation | p.Arg825Gln(p.R825Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22784969:22784969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.704T>C |
| AA Mutation | p.Val235Ala(p.V235A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22882445:22882445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1390G>A |
| AA Mutation | p.Gly464Ser(p.G464S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22913536:22913536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2927C>T |
| AA Mutation | p.Ala976Val(p.A976V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22906815:22906815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534341737 |
| CDS Mutation | c.1994G>A |
| AA Mutation | p.Arg665Gln(p.R665Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22781445:22781445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.86C>T |
| AA Mutation | p.Ala29Val(p.A29V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22882395:22882395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771598124 |
| CDS Mutation | c.1340G>A |
| AA Mutation | p.Arg447His(p.R447H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22882400:22882400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369350136 |
| CDS Mutation | c.1345G>A |
| AA Mutation | p.Val449Met(p.V449M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22863049:22863049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.824G>A |
| AA Mutation | p.Gly275Glu(p.G275E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22784756:22784756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.491G>A |
| AA Mutation | p.Arg164Gln(p.R164Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22863156:22863156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.931A>G |
| AA Mutation | p.Arg311Gly(p.R311G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22910507:22910507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2628T>G |
| AA Mutation | p.Ile876Met(p.I876M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22865110:22865110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1201C>A |
| AA Mutation | p.His401Asn(p.H401N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22865084:22865084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777940741 |
| CDS Mutation | c.1175G>A |
| AA Mutation | p.Arg392His(p.R392H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22864950:22864950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1041C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22908105:22908105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147014777 |
| CDS Mutation | c.2289G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22910435:22910435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2556G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22908054:22908054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2238C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22784631:22784631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747882481 |
| CDS Mutation | c.366G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22913537:22913537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766609166 |
| CDS Mutation | c.2928G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22906828:22906828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751175904 |
| CDS Mutation | c.2007C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22864995:22864995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1086C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000400191 |
| Start | 22913753:22913753(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs563863657 |
| CDS Mutation | c.3059delA |
| AA Mutation | p.Lys1020ArgfsTer63(p.K1020Rfs*63) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000400191 |
| Start | 22906729:22906729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1908C>A |
| AA Mutation | p.Cys636Ter(p.C636*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000400191 |
| Start | 22864890:22864891(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.985dupC |
| AA Mutation | p.Gln329ProfsTer9(p.Q329Pfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |