Primary Site >> Stomach Cancer
Gene >> ITGB6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283249 |
| Start | 160137461:160137461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144967638 |
| CDS Mutation | c.1633G>A |
| AA Mutation | p.Val545Met(p.V545M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283249 |
| Start | 160196277:160196277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.285G>T |
| AA Mutation | p.Gln95His(p.Q95H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283249 |
| Start | 160195535:160195535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140015315 |
| CDS Mutation | c.427G>A |
| AA Mutation | p.Ala143Thr(p.A143T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283249 |
| Start | 160195447:160195447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.515T>C |
| AA Mutation | p.Leu172Pro(p.L172P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283249 |
| Start | 160172714:160172714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760839315 |
| CDS Mutation | c.776G>A |
| AA Mutation | p.Arg259Gln(p.R259Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283249 |
| Start | 160137438:160137438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139038668 |
| CDS Mutation | c.1656C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283249 |
| Start | 160137732:160137732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371228674 |
| CDS Mutation | c.1362C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283249 |
| Start | 160137765:160137765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1329C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283249 |
| Start | 160195521:160195521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61758144 |
| CDS Mutation | c.441C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000283249 |
| Start | 160138199:160138199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1108G>T |
| AA Mutation | p.Glu370Ter(p.E370*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |