Primary Site >> Stomach Cancer
Gene >> SMYD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366957 |
| Start | 214334252:214334252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1165G>A |
| AA Mutation | p.Gly389Arg(p.G389R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366957 |
| Start | 214318909:214318909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.460G>T |
| AA Mutation | p.Ala154Ser(p.A154S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366957 |
| Start | 214318942:214318942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369082796 |
| CDS Mutation | c.493G>A |
| AA Mutation | p.Gly165Arg(p.G165R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366957 |
| Start | 214330982:214330982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146944968 |
| CDS Mutation | c.849C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366957 |
| Start | 214314812:214314813(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.292dupG |
| AA Mutation | p.Glu98GlyfsTer38(p.E98Gfs*38) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366957 |
| Start | 214318107:214318108(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.377_378insC |
| AA Mutation | p.Glu126AspfsTer10(p.E126Dfs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000366957 |
| Start | 214334309:214334309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1221+1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |