Primary Site >> Stomach Cancer
Gene >> TRAF3IP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340026 |
| Start | 111572962:111572962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1250C>T |
| AA Mutation | p.Ser417Leu(p.S417L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340026 |
| Start | 111580237:111580237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751906100 |
| CDS Mutation | c.1009G>A |
| AA Mutation | p.Ala337Thr(p.A337T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340026 |
| Start | 111591871:111591871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.243C>G |
| AA Mutation | p.His81Gln(p.H81Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340026 |
| Start | 111591677:111591677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.437G>A |
| AA Mutation | p.Arg146His(p.R146H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340026 |
| Start | 111575725:111575725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370011231 |
| CDS Mutation | c.1146G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340026 |
| Start | 111591340:111591340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141106401 |
| CDS Mutation | c.774G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |