Primary Site >> Stomach Cancer
Gene >> YTHDF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373812 |
| Start | 28743211:28743211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.941G>A |
| AA Mutation | p.Ser314Asn(p.S314N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373812 |
| Start | 28743706:28743706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1436A>G |
| AA Mutation | p.Tyr479Cys(p.Y479C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373812 |
| Start | 28742500:28742500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377196196 |
| CDS Mutation | c.230C>T |
| AA Mutation | p.Thr77Met(p.T77M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373812 |
| Start | 28743810:28743810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1540C>T |
| AA Mutation | p.Arg514Cys(p.R514C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373812 |
| Start | 28742565:28742565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.295T>G |
| AA Mutation | p.Phe99Val(p.F99V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373812 |
| Start | 28743616:28743616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1346T>C |
| AA Mutation | p.Met449Thr(p.M449T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373812 |
| Start | 28743958:28743958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1688G>A |
| AA Mutation | p.Arg563His(p.R563H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373812 |
| Start | 28743257:28743257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.987G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373812 |
| Start | 28743386:28743386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1116A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373812 |
| Start | 28743677:28743677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375157342 |
| CDS Mutation | c.1407C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373812 |
| Start | 28742671:28742671(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.404delG |
| AA Mutation | p.Gly135GlufsTer26(p.G135Efs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373812 |
| Start | 28738313:28738316(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.110_113delACTT |
| AA Mutation | p.Tyr37Ter(p.Y37*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373812 |
| Start | 28743069:28743069(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.803delC |
| AA Mutation | p.Pro268ArgfsTer2(p.P268Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373812 |
| Start | 28742501:28742501(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.236delG |
| AA Mutation | p.Gly79ValfsTer8(p.G79Vfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000373812 |
| Start | 28742765:28742767(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.497_499delATG |
| AA Mutation | p.Asp166del(p.D166del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |