Primary Site >> Stomach Cancer
Gene >> TBL1X
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9693171:9693171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.914C>T |
| AA Mutation | p.Thr305Met(p.T305M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9697376:9697376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1061T>G |
| AA Mutation | p.Ile354Arg(p.I354R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9654292:9654292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.181T>G |
| AA Mutation | p.Phe61Val(p.F61V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9688075:9688075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.416T>C |
| AA Mutation | p.Met139Thr(p.M139T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9688021:9688021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.362G>A |
| AA Mutation | p.Gly121Asp(p.G121D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9711747:9711747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1576G>A |
| AA Mutation | p.Asp526Asn(p.D526N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9654281:9654281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.170A>G |
| AA Mutation | p.Asp57Gly(p.D57G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9709729:9709729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1408A>G |
| AA Mutation | p.Ser470Gly(p.S470G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9711729:9711729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1558T>G |
| AA Mutation | p.Leu520Val(p.L520V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9709305:9709305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1294G>A |
| AA Mutation | p.Asp432Asn(p.D432N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217964 |
| Start | 9688237:9688237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.578C>T |
| AA Mutation | p.Ala193Val(p.A193V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217964 |
| Start | 9711680:9711680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1509G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217964 |
| Start | 9711677:9711677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767086199 |
| CDS Mutation | c.1506G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217964 |
| Start | 9688157:9688157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369487407 |
| CDS Mutation | c.498T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |