Primary Site >> Stomach Cancer
Gene >> EPHA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143393770:143393770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2597A>G |
| AA Mutation | p.Asp866Gly(p.D866G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143401360:143401360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.396T>G |
| AA Mutation | p.Asp132Glu(p.D132E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143395358:143395358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2044C>A |
| AA Mutation | p.His682Asn(p.H682N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143399705:143399705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140233341 |
| CDS Mutation | c.781C>T |
| AA Mutation | p.Arg261Trp(p.R261W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143399978:143399978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199931138 |
| CDS Mutation | c.508C>T |
| AA Mutation | p.Arg170Cys(p.R170C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143394277:143394277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2419A>G |
| AA Mutation | p.Ser807Gly(p.S807G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143398856:143398856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200253721 |
| CDS Mutation | c.1081C>T |
| AA Mutation | p.Arg361Cys(p.R361C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143397567:143397567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776947009 |
| CDS Mutation | c.1706G>A |
| AA Mutation | p.Arg569Gln(p.R569Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143394242:143394242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2454G>T |
| AA Mutation | p.Glu818Asp(p.E818D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143399954:143399954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745810214 |
| CDS Mutation | c.532C>T |
| AA Mutation | p.Arg178Cys(p.R178C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143399749:143399749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200235266 |
| CDS Mutation | c.737G>A |
| AA Mutation | p.Arg246His(p.R246H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275815 |
| Start | 143394939:143394939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2221A>C |
| AA Mutation | p.Ser741Arg(p.S741R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275815 |
| Start | 143399664:143399664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs562629730 |
| CDS Mutation | c.822C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275815 |
| Start | 143398381:143398381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778014889 |
| CDS Mutation | c.1404G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000275815 |
| Start | 143399327:143399327(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs755617285 |
| CDS Mutation | c.922delG |
| AA Mutation | p.Ala308ProfsTer32(p.A308Pfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |