Primary Site >> Stomach Cancer
Gene >> IGF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300632 |
| Start | 2133632:2133632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369844466 |
| CDS Mutation | c.191G>A |
| AA Mutation | p.Arg64His(p.R64H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300632 |
| Start | 2135454:2135454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.70G>A |
| AA Mutation | p.Ala24Thr(p.A24T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300632 |
| Start | 2133624:2133624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.199G>A |
| AA Mutation | p.Val67Ile(p.V67I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000300632 |
| Start | 2133518:2133518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369122420 |
| CDS Mutation | c.305C>T |
| AA Mutation | p.Pro102Leu(p.P102L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300632 |
| Start | 2135395:2135395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140032633 |
| CDS Mutation | c.129C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300632 |
| Start | 2133026:2133026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200036157 |
| CDS Mutation | c.504C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |