Primary Site >> Stomach Cancer
Gene >> POT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357628 |
| Start | 124863431:124863431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.465T>A |
| AA Mutation | p.Asp155Glu(p.D155E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357628 |
| Start | 124853024:124853024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.817C>T |
| AA Mutation | p.Arg273Trp(p.R273W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357628 |
| Start | 124863483:124863483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.413T>C |
| AA Mutation | p.Val138Ala(p.V138A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357628 |
| Start | 124897169:124897169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5C>A |
| AA Mutation | p.Ser2Tyr(p.S2Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357628 |
| Start | 124853023:124853023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.818G>A |
| AA Mutation | p.Arg273Gln(p.R273Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357628 |
| Start | 124825315:124825315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764901825 |
| CDS Mutation | c.1729G>A |
| AA Mutation | p.Asp577Asn(p.D577N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357628 |
| Start | 124842904:124842904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1066G>A |
| AA Mutation | p.Ala356Thr(p.A356T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357628 |
| Start | 124829289:124829289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1559A>G |
| AA Mutation | p.Asp520Gly(p.D520G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357628 |
| Start | 124842940:124842940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1030G>A |
| AA Mutation | p.Glu344Lys(p.E344K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357628 |
| Start | 124827292:124827292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1608A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000357628 |
| Start | 124846957:124846957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531061783 |
| CDS Mutation | c.991C>T |
| AA Mutation | p.Gln331Ter(p.Q331*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000357628 |
| Start | 124829252:124829252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1594+2T>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |