Primary Site >> Stomach Cancer
Gene >> ATF6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367942 |
| Start | 161792205:161792205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.566C>T |
| AA Mutation | p.Ala189Val(p.A189V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367942 |
| Start | 161863271:161863271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747897836 |
| CDS Mutation | c.1678C>T |
| AA Mutation | p.Arg560Cys(p.R560C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367942 |
| Start | 161819690:161819690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.967T>A |
| AA Mutation | p.Ser323Thr(p.S323T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367942 |
| Start | 161819721:161819721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998G>T |
| AA Mutation | p.Gly333Val(p.G333V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367942 |
| Start | 161784048:161784048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.306C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367942 |
| Start | 161778317:161778317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.156G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367942 |
| Start | 161846509:161846509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1248G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367942 |
| Start | 161958534:161958534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774489243 |
| CDS Mutation | c.1893G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |