Primary Site >> Stomach Cancer
Gene >> CHIA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343320 |
| Start | 111319397:111319397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1106G>A |
| AA Mutation | p.Gly369Asp(p.G369D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343320 |
| Start | 111318574:111318574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs78293817 |
| CDS Mutation | c.811T>G |
| AA Mutation | p.Phe271Val(p.F271V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000343320 |
| Start | 111311718:111311718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769844294 |
| CDS Mutation | c.55G>A |
| AA Mutation | p.Gly19Ser(p.G19S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343320 |
| Start | 111315341:111315341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.386A>C |
| AA Mutation | p.Gln129Pro(p.Q129P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343320 |
| Start | 111317687:111317687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139158262 |
| CDS Mutation | c.487C>T |
| AA Mutation | p.Arg163Cys(p.R163C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343320 |
| Start | 111315279:111315279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.324C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343320 |
| Start | 111318076:111318076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560491782 |
| CDS Mutation | c.696G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |