Primary Site >> Stomach Cancer
Gene >> RTKN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272430 |
| Start | 74426269:74426269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1666C>T |
| AA Mutation | p.Arg556Cys(p.R556C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000272430 |
| Start | 74432467:74432467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758078564 |
| CDS Mutation | c.311G>A |
| AA Mutation | p.Arg104Gln(p.R104Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272430 |
| Start | 74430669:74430669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.320A>G |
| AA Mutation | p.Asp107Gly(p.D107G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272430 |
| Start | 74430016:74430016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.567T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000272430 |
| Start | 74429870:74429870(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs756896464 |
| CDS Mutation | c.713delG |
| AA Mutation | p.Gly238ValfsTer70(p.G238Vfs*70) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000272430 |
| Start | 74426323:74426323(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1612delC |
| AA Mutation | p.Leu538SerfsTer117(p.L538Sfs*117) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000272430 |
| Start | 74426386:74426386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs78574572 |
| CDS Mutation | c.1549C>T |
| AA Mutation | p.Arg517Ter(p.R517*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |