Primary Site >> Stomach Cancer
Gene >> GRAP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344138 |
| Start | 39970924:39970924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761211125 |
| CDS Mutation | c.833C>T |
| AA Mutation | p.Ala278Val(p.A278V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344138 |
| Start | 39969495:39969495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.775C>T |
| AA Mutation | p.Arg259Trp(p.R259W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344138 |
| Start | 39968049:39968049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.467G>A |
| AA Mutation | p.Arg156Gln(p.R156Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344138 |
| Start | 39969496:39969496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.776G>A |
| AA Mutation | p.Arg259Gln(p.R259Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344138 |
| Start | 39969418:39969418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.698G>T |
| AA Mutation | p.Arg233Leu(p.R233L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344138 |
| Start | 39955851:39955851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771896318 |
| CDS Mutation | c.111G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344138 |
| Start | 39970973:39970973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201763751 |
| CDS Mutation | c.882C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |