Primary Site >> Stomach Cancer
Gene >> SIX3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942889:44942889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.785G>A |
| AA Mutation | p.Arg262His(p.R262H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942199:44942199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.95G>A |
| AA Mutation | p.Ser32Asn(p.S32N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942910:44942910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.806G>T |
| AA Mutation | p.Arg269Met(p.R269M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942445:44942445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.341C>T |
| AA Mutation | p.Ser114Leu(p.S114L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942200:44942200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202214767 |
| CDS Mutation | c.96C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942506:44942506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.402G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942509:44942509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.405C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942722:44942722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.618C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942833:44942833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.729C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942470:44942470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.366C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260653 |
| Start | 44944631:44944631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.870G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260653 |
| Start | 44942319:44942319(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs763853335 |
| CDS Mutation | c.221delC |
| AA Mutation | p.Pro74ArgfsTer177(p.P74Rfs*177) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |