Primary Site >> Stomach Cancer
Gene >> BIRC3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263464 |
| Start | 102325281:102325281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.772C>T |
| AA Mutation | p.Arg258Cys(p.R258C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263464 |
| Start | 102325501:102325501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.889G>A |
| AA Mutation | p.Gly297Ser(p.G297S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263464 |
| Start | 102324979:102324979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.470T>C |
| AA Mutation | p.Leu157Ser(p.L157S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263464 |
| Start | 102324608:102324608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.99G>C |
| AA Mutation | p.Met33Ile(p.M33I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263464 |
| Start | 102325189:102325189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.680G>T |
| AA Mutation | p.Arg227Ile(p.R227I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263464 |
| Start | 102325159:102325159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768158423 |
| CDS Mutation | c.650C>T |
| AA Mutation | p.Pro217Leu(p.P217L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263464 |
| Start | 102324937:102324937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.428C>T |
| AA Mutation | p.Ser143Leu(p.S143L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263464 |
| Start | 102324861:102324861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.352A>T |
| AA Mutation | p.Thr118Ser(p.T118S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263464 |
| Start | 102324812:102324812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374571638 |
| CDS Mutation | c.303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263464 |
| Start | 102324760:102324760(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.254delA |
| AA Mutation | p.Lys85SerfsTer15(p.K85Sfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000263464 |
| Start | 102325538:102325538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.926G>A |
| AA Mutation | p.Trp309Ter(p.W309*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263464 |
| Start | 102336939:102336940(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1654_1673dupCAAGAAGAAAGAACATGTAA |
| AA Mutation | p.Lys558AsnfsTer17(p.K558Nfs*17) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |