Primary Site >> Stomach Cancer
Gene >> MAPT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262410 |
| Start | 45983676:45983676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.872G>A |
| AA Mutation | p.Arg291Gln(p.R291Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262410 |
| Start | 45983761:45983761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.957G>T |
| AA Mutation | p.Glu319Asp(p.E319D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262410 |
| Start | 45996630:45996630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1739C>A |
| AA Mutation | p.Thr580Asn(p.T580N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262410 |
| Start | 45983535:45983535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192840932 |
| CDS Mutation | c.731G>A |
| AA Mutation | p.Arg244Gln(p.R244Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262410 |
| Start | 45990071:45990071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1376T>G |
| AA Mutation | p.Leu459Arg(p.L459R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262410 |
| Start | 45983634:45983634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.830C>T |
| AA Mutation | p.Thr277Ile(p.T277I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262410 |
| Start | 45996587:45996587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1696C>T |
| AA Mutation | p.Pro566Ser(p.P566S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262410 |
| Start | 45996547:45996547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115142761 |
| CDS Mutation | c.1656G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262410 |
| Start | 45962454:45962454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs63750529 |
| CDS Mutation | c.117G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262410 |
| Start | 46024117:46024117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2223G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262410 |
| Start | 45962379:45962379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759306195 |
| CDS Mutation | c.42C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262410 |
| Start | 46024054:46024054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs116567476 |
| CDS Mutation | c.2160G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262410 |
| Start | 46024120:46024120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200637464 |
| CDS Mutation | c.2226C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262410 |
| Start | 45983227:45983227(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.428delC |
| AA Mutation | p.Pro143GlnfsTer3(p.P143Qfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262410 |
| Start | 45962415:45962415(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.83delG |
| AA Mutation | p.Gly28AlafsTer16(p.G28Afs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000262410 |
| Start | 45983287:45983288(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.483_484insTTTTCTGCTTGTTAGTGGGTGACCAAAT |
| AA Mutation | p.Gly162PhefsTer5(p.G162Ffs*5) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |