Primary Site >> Stomach Cancer
Gene >> USP47
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000399455 |
| Start | 11905547:11905547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1028T>C |
| AA Mutation | p.Val343Ala(p.V343A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399455 |
| Start | 11922793:11922793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1348A>T |
| AA Mutation | p.Met450Leu(p.M450L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399455 |
| Start | 11892013:11892013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.463G>T |
| AA Mutation | p.Gly155Cys(p.G155C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399455 |
| Start | 11884539:11884539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.376C>T |
| AA Mutation | p.His126Tyr(p.H126Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399455 |
| Start | 11952770:11952770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3673C>T |
| AA Mutation | p.Leu1225Phe(p.L1225F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399455 |
| Start | 11905484:11905484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.965A>G |
| AA Mutation | p.Asp322Gly(p.D322G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000399455 |
| Start | 11952870:11952870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3773A>C |
| AA Mutation | p.Lys1258Thr(p.K1258T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399455 |
| Start | 11905443:11905443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.924C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399455 |
| Start | 11936431:11936431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368349531 |
| CDS Mutation | c.2058C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399455 |
| Start | 11948075:11948075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3282C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399455 |
| Start | 11938315:11938358(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2201_2244delTTCGTGCTTACTTAAATCAGACAGTTACAGAATTCAAACAACTG |
| AA Mutation | p.Val734AspfsTer10(p.V734Dfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000399455 |
| Start | 11933090:11933090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776574999 |
| CDS Mutation | c.1798C>T |
| AA Mutation | p.Arg600Ter(p.R600*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399455 |
| Start | 11943009:11943010(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3048_3049insCGTTCTTC |
| AA Mutation | p.Ser1017ArgfsTer39(p.S1017Rfs*39) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |