Primary Site >> Stomach Cancer
Gene >> PML
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74022871:74022871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.646G>A |
| AA Mutation | p.Ala216Thr(p.A216T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74032672:74032672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1355T>C |
| AA Mutation | p.Val452Ala(p.V452A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74023370:74023370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149871195 |
| CDS Mutation | c.1145G>A |
| AA Mutation | p.Arg382His(p.R382H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 73998383:73998383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200708179 |
| CDS Mutation | c.509G>A |
| AA Mutation | p.Arg170His(p.R170H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74023372:74023372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1147C>A |
| AA Mutation | p.Leu383Met(p.L383M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74044245:74044245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1886C>T |
| AA Mutation | p.Ala629Val(p.A629V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74023303:74023303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1078C>T |
| AA Mutation | p.Arg360Cys(p.R360C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74023133:74023133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754797325 |
| CDS Mutation | c.908C>T |
| AA Mutation | p.Ala303Val(p.A303V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 73998458:73998458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.584G>A |
| AA Mutation | p.Arg195His(p.R195H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74023096:74023096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.871C>T |
| AA Mutation | p.Arg291Trp(p.R291W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 73998125:73998125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771298279 |
| CDS Mutation | c.251C>T |
| AA Mutation | p.Ser84Leu(p.S84L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74034502:74034502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1682G>A |
| AA Mutation | p.Ser561Asn(p.S561N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74024911:74024911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1238C>T |
| AA Mutation | p.Pro413Leu(p.P413L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268058 |
| Start | 74023323:74023323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1098C>A |
| AA Mutation | p.Ser366Arg(p.S366R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268058 |
| Start | 74033404:74033404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748216241 |
| CDS Mutation | c.1647C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268058 |
| Start | 74022963:74022963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.738G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268058 |
| Start | 73998123:73998123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs572620428 |
| CDS Mutation | c.249G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |