Primary Site >> Stomach Cancer
Gene >> ACO2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216254 |
| Start | 41508039:41508039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370417583 |
| CDS Mutation | c.422G>A |
| AA Mutation | p.Arg141His(p.R141H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216254 |
| Start | 41507877:41507877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777420895 |
| CDS Mutation | c.260C>T |
| AA Mutation | p.Ser87Leu(p.S87L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216254 |
| Start | 41528548:41528548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115203053 |
| CDS Mutation | c.2278G>A |
| AA Mutation | p.Glu760Lys(p.E760K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216254 |
| Start | 41522962:41522962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752600434 |
| CDS Mutation | c.1271G>A |
| AA Mutation | p.Arg424His(p.R424H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216254 |
| Start | 41526397:41526397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1897C>T |
| AA Mutation | p.Arg633Cys(p.R633C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216254 |
| Start | 41524919:41524919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1556G>A |
| AA Mutation | p.Gly519Asp(p.G519D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216254 |
| Start | 41526361:41526361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1861G>A |
| AA Mutation | p.Ala621Thr(p.A621T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216254 |
| Start | 41527388:41527388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2054C>T |
| AA Mutation | p.Ala685Val(p.A685V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216254 |
| Start | 41527302:41527302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377371545 |
| CDS Mutation | c.1968G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216254 |
| Start | 41523890:41523890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200407418 |
| CDS Mutation | c.1431G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000216254 |
| Start | 41527349:41527355(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2018_2024delATGCAGC |
| AA Mutation | p.His673LeufsTer25(p.H673Lfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000216254 |
| Start | 41523845:41523845(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1390delG |
| AA Mutation | p.Glu464ArgfsTer51(p.E464Rfs*51) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |