Primary Site >> Stomach Cancer
Gene >> PRPF40B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380281 |
| Start | 49635459:49635459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1195G>A |
| AA Mutation | p.Ala399Thr(p.A399T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380281 |
| Start | 49631440:49631440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.58G>T |
| AA Mutation | p.Gly20Trp(p.G20W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380281 |
| Start | 49634451:49634451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.866A>G |
| AA Mutation | p.Asp289Gly(p.D289G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000380281 |
| Start | 49633546:49633546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.513G>T |
| AA Mutation | p.Glu171Asp(p.E171D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380281 |
| Start | 49636840:49636840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1485G>T |
| AA Mutation | p.Glu495Asp(p.E495D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380281 |
| Start | 49642958:49642958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768250601 |
| CDS Mutation | c.2084G>A |
| AA Mutation | p.Gly695Asp(p.G695D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380281 |
| Start | 49635868:49635868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145239236 |
| CDS Mutation | c.1235G>A |
| AA Mutation | p.Arg412His(p.R412H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380281 |
| Start | 49635239:49635239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542656887 |
| CDS Mutation | c.1076G>A |
| AA Mutation | p.Arg359His(p.R359H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380281 |
| Start | 49642353:49642353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1937T>C |
| AA Mutation | p.Leu646Pro(p.L646P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380281 |
| Start | 49631435:49631435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533114278 |
| CDS Mutation | c.53C>T |
| AA Mutation | p.Pro18Leu(p.P18L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380281 |
| Start | 49641994:49641994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139833340 |
| CDS Mutation | c.1788C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |