Primary Site >> Stomach Cancer
Gene >> CPOX
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264193 |
| Start | 98581497:98581497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1187A>G |
| AA Mutation | p.Asn396Ser(p.N396S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264193 |
| Start | 98580709:98580709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs28931603 |
| CDS Mutation | c.1339C>T |
| AA Mutation | p.Arg447Cys(p.R447C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264193 |
| Start | 98588824:98588824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.842G>A |
| AA Mutation | p.Cys281Tyr(p.C281Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264193 |
| Start | 98581441:98581441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1243G>C |
| AA Mutation | p.Glu415Gln(p.E415Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264193 |
| Start | 98581433:98581433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1251C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000264193 |
| Start | 98581408:98581408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202148820 |
| CDS Mutation | c.1276C>T |
| AA Mutation | p.Arg426Ter(p.R426*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |