Primary Site >> Stomach Cancer
Gene >> MRPL28
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000199706 |
| Start | 369105:369105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.404T>A |
| AA Mutation | p.Ile135Asn(p.I135N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000199706 |
| Start | 369990:369990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.229C>T |
| AA Mutation | p.Arg77Trp(p.R77W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000199706 |
| Start | 368565:368565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.512G>A |
| AA Mutation | p.Arg171Gln(p.R171Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000199706 |
| Start | 368359:368359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.632C>T |
| AA Mutation | p.Ala211Val(p.A211V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000199706 |
| Start | 369103:369103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749118796 |
| CDS Mutation | c.406G>A |
| AA Mutation | p.Asp136Asn(p.D136N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000199706 |
| Start | 369175:369175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776729941 |
| CDS Mutation | c.334C>T |
| AA Mutation | p.Arg112Ter(p.R112*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |