Primary Site >> Stomach Cancer
Gene >> ME3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393324 |
| Start | 86447202:86447202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1243G>A |
| AA Mutation | p.Ala415Thr(p.A415T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393324 |
| Start | 86559711:86559711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.296G>A |
| AA Mutation | p.Arg99Gln(p.R99Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393324 |
| Start | 86498076:86498076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.592G>T |
| AA Mutation | p.Gly198Cys(p.G198C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393324 |
| Start | 86447148:86447148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1297C>T |
| AA Mutation | p.His433Tyr(p.H433Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393324 |
| Start | 86556674:86556674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777588552 |
| CDS Mutation | c.346C>T |
| AA Mutation | p.Arg116Trp(p.R116W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393324 |
| Start | 86447179:86447179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749644334 |
| CDS Mutation | c.1266G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393324 |
| Start | 86498023:86498023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149425348 |
| CDS Mutation | c.645C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393324 |
| Start | 86450358:86450358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.960G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393324 |
| Start | 86556606:86556606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368673093 |
| CDS Mutation | c.414G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000393324 |
| Start | 86446473:86446473(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1395delT |
| AA Mutation | p.Phe465LeufsTer10(p.F465Lfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000393324 |
| Start | 86559798:86559799(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.208dupA |
| AA Mutation | p.Arg70LysfsTer34(p.R70Kfs*34) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |