Primary Site >> Stomach Cancer
Gene >> MTMR11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000439741 |
| Start | 149933658:149933658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812G>T |
| AA Mutation | p.Arg271Leu(p.R271L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000439741 |
| Start | 149933856:149933856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782450905 |
| CDS Mutation | c.770C>T |
| AA Mutation | p.Pro257Leu(p.P257L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000439741 |
| Start | 149931414:149931414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1136G>A |
| AA Mutation | p.Arg379His(p.R379H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000439741 |
| Start | 149933664:149933664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.806T>G |
| AA Mutation | p.Leu269Arg(p.L269R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000439741 |
| Start | 149933421:149933421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.970G>A |
| AA Mutation | p.Ala324Thr(p.A324T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000439741 |
| Start | 149931261:149931261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1289A>T |
| AA Mutation | p.Glu430Val(p.E430V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000439741 |
| Start | 149931325:149931325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782759787 |
| CDS Mutation | c.1225C>T |
| AA Mutation | p.Arg409Ter(p.R409*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |