Primary Site >> Stomach Cancer
Gene >> ALDH3A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225740 |
| Start | 19742070:19742070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545679214 |
| CDS Mutation | c.623C>T |
| AA Mutation | p.Thr208Met(p.T208M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225740 |
| Start | 19740344:19740344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.941G>A |
| AA Mutation | p.Arg314His(p.R314H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225740 |
| Start | 19743414:19743414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.212T>C |
| AA Mutation | p.Ile71Thr(p.I71T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225740 |
| Start | 19743298:19743298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140767140 |
| CDS Mutation | c.328G>A |
| AA Mutation | p.Val110Ile(p.V110I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225740 |
| Start | 19742089:19742089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.604A>G |
| AA Mutation | p.Lys202Glu(p.K202E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000225740 |
| Start | 19740469:19740469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553737482 |
| CDS Mutation | c.816C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000225740 |
| Start | 19738413:19738413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770963389 |
| CDS Mutation | c.1257C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000225740 |
| Start | 19743254:19743254(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.372delC |
| AA Mutation | p.Met125TrpfsTer18(p.M125Wfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000225740 |
| Start | 19738336:19738336(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs778623472 |
| CDS Mutation | c.1334delC |
| AA Mutation | p.Pro445ArgfsTer6(p.P445Rfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |