Primary Site >> Stomach Cancer
Gene >> PIAS4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262971 |
| Start | 4037405:4037405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1174G>T |
| AA Mutation | p.Asp392Tyr(p.D392Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262971 |
| Start | 4013169:4013169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754930081 |
| CDS Mutation | c.274C>T |
| AA Mutation | p.Arg92Trp(p.R92W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262971 |
| Start | 4024036:4024036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.455T>C |
| AA Mutation | p.Val152Ala(p.V152A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262971 |
| Start | 4013160:4013160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.265A>G |
| AA Mutation | p.Thr89Ala(p.T89A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262971 |
| Start | 4037485:4037485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1254G>T |
| AA Mutation | p.Gln418His(p.Q418H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262971 |
| Start | 4033137:4033137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.945C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262971 |
| Start | 4037659:4037659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1317C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262971 |
| Start | 4037449:4037449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767696160 |
| CDS Mutation | c.1218G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262971 |
| Start | 4037626:4037626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371055074 |
| CDS Mutation | c.1284C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262971 |
| Start | 4028170:4028170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201647511 |
| CDS Mutation | c.564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262971 |
| Start | 4013141:4013141(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.250delC |
| AA Mutation | p.Leu84Ter(p.L84*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262971 |
| Start | 4037646:4037646(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1308delC |
| AA Mutation | p.Ser437AlafsTer156(p.S437Afs*156) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |