Primary Site >> Stomach Cancer
Gene >> CCT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299300 |
| Start | 69586787:69586787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.113T>C |
| AA Mutation | p.Leu38Ser(p.L38S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299300 |
| Start | 69598334:69598334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746543261 |
| CDS Mutation | c.1348A>G |
| AA Mutation | p.Ile450Val(p.I450V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299300 |
| Start | 69588192:69588192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.376A>G |
| AA Mutation | p.Ile126Val(p.I126V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299300 |
| Start | 69597227:69597227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1054G>A |
| AA Mutation | p.Val352Ile(p.V352I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299300 |
| Start | 69597728:69597728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201201152 |
| CDS Mutation | c.1193C>T |
| AA Mutation | p.Ala398Val(p.A398V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299300 |
| Start | 69588196:69588196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.380T>C |
| AA Mutation | p.Ile127Thr(p.I127T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299300 |
| Start | 69588199:69588199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545752398 |
| CDS Mutation | c.383C>T |
| AA Mutation | p.Ala128Val(p.A128V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |