Primary Site >> Stomach Cancer
Gene >> PPM1E
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308249 |
| Start | 58980145:58980145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1382G>A |
| AA Mutation | p.Ser461Asn(p.S461N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308249 |
| Start | 58965741:58965741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754324408 |
| CDS Mutation | c.631G>A |
| AA Mutation | p.Glu211Lys(p.E211K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308249 |
| Start | 58969701:58969701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199549502 |
| CDS Mutation | c.946C>T |
| AA Mutation | p.Arg316Trp(p.R316W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308249 |
| Start | 58955717:58955717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.533T>C |
| AA Mutation | p.Leu178Pro(p.L178P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308249 |
| Start | 58980924:58980924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2161C>T |
| AA Mutation | p.Pro721Ser(p.P721S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308249 |
| Start | 58980084:58980084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778605375 |
| CDS Mutation | c.1321G>A |
| AA Mutation | p.Val441Met(p.V441M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308249 |
| Start | 58980807:58980807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2044A>G |
| AA Mutation | p.Arg682Gly(p.R682G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308249 |
| Start | 58980775:58980775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770018116 |
| CDS Mutation | c.2012G>A |
| AA Mutation | p.Arg671His(p.R671H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308249 |
| Start | 58972909:58972909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1194G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308249 |
| Start | 58756108:58756108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779475307 |
| CDS Mutation | c.111C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |