Primary Site >> Stomach Cancer
Gene >> PACS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325438 |
| Start | 105368504:105368504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782151393 |
| CDS Mutation | c.706C>T |
| AA Mutation | p.Arg236Trp(p.R236W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325438 |
| Start | 105383505:105383505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1760T>A |
| AA Mutation | p.Ile587Asn(p.I587N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325438 |
| Start | 105376897:105376897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782607135 |
| CDS Mutation | c.931G>A |
| AA Mutation | p.Val311Ile(p.V311I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325438 |
| Start | 105369847:105369847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.748A>T |
| AA Mutation | p.Asn250Tyr(p.N250Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325438 |
| Start | 105367322:105367322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.533C>A |
| AA Mutation | p.Pro178His(p.P178H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325438 |
| Start | 105368133:105368133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200599760 |
| CDS Mutation | c.646G>A |
| AA Mutation | p.Ala216Thr(p.A216T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325438 |
| Start | 105393294:105393294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2510G>C |
| AA Mutation | p.Arg837Pro(p.R837P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325438 |
| Start | 105376834:105376834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.868T>C |
| AA Mutation | p.Tyr290His(p.Y290H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325438 |
| Start | 105383438:105383438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782038571 |
| CDS Mutation | c.1693C>T |
| AA Mutation | p.Arg565Trp(p.R565W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325438 |
| Start | 105376779:105376779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782081321 |
| CDS Mutation | c.813G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325438 |
| Start | 105380962:105380962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1131G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325438 |
| Start | 105382878:105382878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370005025 |
| CDS Mutation | c.1578G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |