Primary Site >> Stomach Cancer
Gene >> MACROD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217246 |
| Start | 14002321:14002321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.80G>A |
| AA Mutation | p.Arg27His(p.R27H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217246 |
| Start | 15499825:15499825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.623G>T |
| AA Mutation | p.Trp208Leu(p.W208L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217246 |
| Start | 14684894:14684894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557866799 |
| CDS Mutation | c.353G>A |
| AA Mutation | p.Arg118His(p.R118H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217246 |
| Start | 15967584:15967584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773610273 |
| CDS Mutation | c.939C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217246 |
| Start | 15229974:15229974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.453C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217246 |
| Start | 14684868:14684868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371771933 |
| CDS Mutation | c.327C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |