Primary Site >> Stomach Cancer
Gene >> MECP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303391 |
| Start | 154031302:154031302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186663314 |
| CDS Mutation | c.526C>T |
| AA Mutation | p.Pro176Ser(p.P176S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303391 |
| Start | 154032352:154032352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.232T>G |
| AA Mutation | p.Ser78Ala(p.S78A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303391 |
| Start | 154030455:154030455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs185957513 |
| CDS Mutation | c.1373G>A |
| AA Mutation | p.Arg458His(p.R458H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303391 |
| Start | 154032549:154032549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.35A>G |
| AA Mutation | p.Lys12Arg(p.K12R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303391 |
| Start | 154032529:154032529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.55C>G |
| AA Mutation | p.Gln19Glu(p.Q19E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303391 |
| Start | 154032268:154032268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs28934907 |
| CDS Mutation | c.316C>T |
| AA Mutation | p.Arg106Trp(p.R106W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303391 |
| Start | 154030372:154030372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1456A>C |
| AA Mutation | p.Ser486Arg(p.S486R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303391 |
| Start | 154030640:154030640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781816931 |
| CDS Mutation | c.1188C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303391 |
| Start | 154030606:154030606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1222T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303391 |
| Start | 154031117:154031118(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs267608517 |
| CDS Mutation | c.710dupG |
| AA Mutation | p.Gly238TrpfsTer21(p.G238Wfs*21) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |