Primary Site >> Stomach Cancer
Gene >> TMEM8B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377988 |
| Start | 35853554:35853554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199969691 |
| CDS Mutation | c.1133G>A |
| AA Mutation | p.Arg378His(p.R378H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377988 |
| Start | 35853662:35853662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1241A>T |
| AA Mutation | p.His414Leu(p.H414L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000377988 |
| Start | 35846381:35846381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.497G>A |
| AA Mutation | p.Arg166Gln(p.R166Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377988 |
| Start | 35846853:35846853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.677C>T |
| AA Mutation | p.Ala226Val(p.A226V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377988 |
| Start | 35853174:35853174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748640951 |
| CDS Mutation | c.1000A>G |
| AA Mutation | p.Met334Val(p.M334V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377988 |
| Start | 35852858:35852858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.851T>C |
| AA Mutation | p.Val284Ala(p.V284A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377988 |
| Start | 35853161:35853161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.987T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377988 |
| Start | 35852922:35852922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201246215 |
| CDS Mutation | c.915C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000377988 |
| Start | 35846366:35846385(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.486_497+8delGGTGGGGCCTCGGTGAGCGG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |