Primary Site >> Esophagus Cancer
Gene >> TENM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124385931:124385931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5801G>A |
| AA Mutation | p.Arg1934Gln(p.R1934Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124705148:124705148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.880C>A |
| AA Mutation | p.Pro294Thr(p.P294T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124645248:124645248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201117886 |
| CDS Mutation | c.1771G>A |
| AA Mutation | p.Val591Ile(p.V591I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124705144:124705144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.884T>C |
| AA Mutation | p.Leu295Pro(p.L295P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124497194:124497194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3517G>A |
| AA Mutation | p.Gly1173Ser(p.G1173S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124520739:124520739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3079A>C |
| AA Mutation | p.Ser1027Arg(p.S1027R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124895989:124895989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.470G>A |
| AA Mutation | p.Gly157Glu(p.G157E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124523533:124523533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2864G>C |
| AA Mutation | p.Trp955Ser(p.W955S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124546913:124546913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2612G>A |
| AA Mutation | p.Ser871Asn(p.S871N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124381007:124381007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7707G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |