Primary Site >> Stomach Cancer
Gene >> PTPN6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318974 |
| Start | 6955431:6955431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.693C>A |
| AA Mutation | p.Asn231Lys(p.N231K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318974 |
| Start | 6954836:6954836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.358G>A |
| AA Mutation | p.Ala120Thr(p.A120T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318974 |
| Start | 6955481:6955481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.743T>C |
| AA Mutation | p.Phe248Ser(p.F248S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318974 |
| Start | 6956461:6956461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.967G>A |
| AA Mutation | p.Ala323Thr(p.A323T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318974 |
| Start | 6960171:6960171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1513T>C |
| AA Mutation | p.Tyr505His(p.Y505H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318974 |
| Start | 6955733:6955733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.821A>G |
| AA Mutation | p.Asn274Ser(p.N274S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318974 |
| Start | 6958026:6958026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1314G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318974 |
| Start | 6956445:6956445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200624825 |
| CDS Mutation | c.951C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318974 |
| Start | 6957743:6957743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374040175 |
| CDS Mutation | c.1164C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318974 |
| Start | 6960185:6960185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371456901 |
| CDS Mutation | c.1527C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000318974 |
| Start | 6952035:6952077(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.184_226delGACCTGTATGGAGGGGAGAAGTTTGCGACTCTGACAGAGCTGG |
| AA Mutation | p.Asp62TrpfsTer25(p.D62Wfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |