Primary Site >> Stomach Cancer
Gene >> ETS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319397 |
| Start | 128521937:128521937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.58G>A |
| AA Mutation | p.Asp20Asn(p.D20N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319397 |
| Start | 128480250:128480250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.932G>A |
| AA Mutation | p.Arg311His(p.R311H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319397 |
| Start | 128462369:128462369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768471010 |
| CDS Mutation | c.1318G>A |
| AA Mutation | p.Asp440Asn(p.D440N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319397 |
| Start | 128480299:128480299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.883C>A |
| AA Mutation | p.Leu295Met(p.L295M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319397 |
| Start | 128463612:128463612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1007A>G |
| AA Mutation | p.Gln336Arg(p.Q336R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319397 |
| Start | 128480257:128480257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766964257 |
| CDS Mutation | c.925C>T |
| AA Mutation | p.Arg309Trp(p.R309W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319397 |
| Start | 128480251:128480251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763167051 |
| CDS Mutation | c.931C>T |
| AA Mutation | p.Arg311Cys(p.R311C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319397 |
| Start | 128484863:128484863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747494573 |
| CDS Mutation | c.690C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |