Primary Site >> Stomach Cancer
Gene >> TBX21
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000177694 |
| Start | 47745260:47745260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769911299 |
| CDS Mutation | c.1502G>A |
| AA Mutation | p.Arg501His(p.R501H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000177694 |
| Start | 47745212:47745212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757029551 |
| CDS Mutation | c.1454C>T |
| AA Mutation | p.Pro485Leu(p.P485L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000177694 |
| Start | 47744888:47744888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199527603 |
| CDS Mutation | c.1130C>T |
| AA Mutation | p.Ala377Val(p.A377V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000177694 |
| Start | 47745312:47745312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1554T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000177694 |
| Start | 47744799:47744799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1041T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000177694 |
| Start | 47745237:47745237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768130755 |
| CDS Mutation | c.1479C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000177694 |
| Start | 47743168:47743168(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.748delG |
| AA Mutation | p.Ala250ArgfsTer5(p.A250Rfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000177694 |
| Start | 47744924:47744924(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1171delC |
| AA Mutation | p.Arg391GlyfsTer14(p.R391Gfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000177694 |
| Start | 47745175:47745175(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1422delC |
| AA Mutation | p.Leu475TrpfsTer66(p.L475Wfs*66) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |