Primary Site >> Stomach Cancer
Gene >> SH2B1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322610 |
| Start | 28867026:28867026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.932C>A |
| AA Mutation | p.Pro311Gln(p.P311Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322610 |
| Start | 28866809:28866809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769421511 |
| CDS Mutation | c.715G>A |
| AA Mutation | p.Ala239Thr(p.A239T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322610 |
| Start | 28873450:28873450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747265054 |
| CDS Mutation | c.1901C>T |
| AA Mutation | p.Pro634Leu(p.P634L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322610 |
| Start | 28866561:28866561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.467G>A |
| AA Mutation | p.Arg156His(p.R156H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322610 |
| Start | 28872579:28872579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1771C>T |
| AA Mutation | p.His591Tyr(p.H591Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322610 |
| Start | 28866966:28866966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765409318 |
| CDS Mutation | c.872G>A |
| AA Mutation | p.Arg291His(p.R291H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322610 |
| Start | 28866618:28866618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.524C>T |
| AA Mutation | p.Thr175Ile(p.T175I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322610 |
| Start | 28872221:28872221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370851725 |
| CDS Mutation | c.1545C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |