Primary Site >> Stomach Cancer
Gene >> CTTN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301843 |
| Start | 70415687:70415687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.427G>A |
| AA Mutation | p.Gly143Arg(p.G143R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301843 |
| Start | 70433215:70433215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1381G>A |
| AA Mutation | p.Gly461Ser(p.G461S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301843 |
| Start | 70420486:70420486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.766T>A |
| AA Mutation | p.Leu256Met(p.L256M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301843 |
| Start | 70431233:70431233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534661512 |
| CDS Mutation | c.1219G>A |
| AA Mutation | p.Ala407Thr(p.A407T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301843 |
| Start | 70433695:70433695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1493T>C |
| AA Mutation | p.Val498Ala(p.V498A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301843 |
| Start | 70431228:70431228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61885860 |
| CDS Mutation | c.1214C>T |
| AA Mutation | p.Ser405Leu(p.S405L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301843 |
| Start | 70419833:70419833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373870325 |
| CDS Mutation | c.656C>T |
| AA Mutation | p.Thr219Met(p.T219M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301843 |
| Start | 70435155:70435155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778284858 |
| CDS Mutation | c.1646G>A |
| AA Mutation | p.Arg549Gln(p.R549Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301843 |
| Start | 70407550:70407550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.120T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301843 |
| Start | 70433705:70433705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112839434 |
| CDS Mutation | c.1503C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |