Primary Site >> Stomach Cancer
Gene >> TEAD4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359864 |
| Start | 3022010:3022010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.890A>C |
| AA Mutation | p.Lys297Thr(p.K297T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359864 |
| Start | 3021944:3021944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373793296 |
| CDS Mutation | c.824C>T |
| AA Mutation | p.Pro275Leu(p.P275L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359864 |
| Start | 3017418:3017418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.375G>C |
| AA Mutation | p.Lys125Asn(p.K125N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359864 |
| Start | 3019161:3019161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370063341 |
| CDS Mutation | c.574C>T |
| AA Mutation | p.Pro192Ser(p.P192S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359864 |
| Start | 3017498:3017498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.455G>A |
| AA Mutation | p.Arg152Gln(p.R152Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359864 |
| Start | 3020679:3020679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199662990 |
| CDS Mutation | c.629C>T |
| AA Mutation | p.Pro210Leu(p.P210L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359864 |
| Start | 3020675:3020675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.625C>T |
| AA Mutation | p.Pro209Ser(p.P209S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359864 |
| Start | 3020676:3020676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755432905 |
| CDS Mutation | c.626C>T |
| AA Mutation | p.Pro209Leu(p.P209L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359864 |
| Start | 3021913:3021913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201149385 |
| CDS Mutation | c.793G>A |
| AA Mutation | p.Val265Met(p.V265M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359864 |
| Start | 3019157:3019157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.570G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359864 |
| Start | 3040391:3040391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1218G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359864 |
| Start | 2994976:2994976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148965461 |
| CDS Mutation | c.210C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |