Primary Site >> Stomach Cancer
Gene >> MACC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332878 |
| Start | 20158310:20158310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2051T>A |
| AA Mutation | p.Ile684Asn(p.I684N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332878 |
| Start | 20159238:20159238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1123T>A |
| AA Mutation | p.Tyr375Asn(p.Y375N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332878 |
| Start | 20159091:20159091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1270T>G |
| AA Mutation | p.Ser424Ala(p.S424A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332878 |
| Start | 20141028:20141028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759723845 |
| CDS Mutation | c.2477G>A |
| AA Mutation | p.Arg826Lys(p.R826K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332878 |
| Start | 20159729:20159729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.632A>G |
| AA Mutation | p.Glu211Gly(p.E211G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332878 |
| Start | 20141147:20141147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2358A>T |
| AA Mutation | p.Lys786Asn(p.K786N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332878 |
| Start | 20159805:20159805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769884185 |
| CDS Mutation | c.556C>T |
| AA Mutation | p.Arg186Cys(p.R186C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332878 |
| Start | 20161832:20161832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.31T>C |
| AA Mutation | p.Ser11Pro(p.S11P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332878 |
| Start | 20159804:20159804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375276990 |
| CDS Mutation | c.557G>A |
| AA Mutation | p.Arg186His(p.R186H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332878 |
| Start | 20158774:20158774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1587T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000332878 |
| Start | 20141026:20141026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776961275 |
| CDS Mutation | c.2479G>T |
| AA Mutation | p.Glu827Ter(p.E827*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |