Primary Site >> Stomach Cancer
Gene >> MAPK8IP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241014 |
| Start | 45905037:45905037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1960A>C |
| AA Mutation | p.Asn654His(p.N654H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241014 |
| Start | 45902956:45902956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768339614 |
| CDS Mutation | c.1189C>T |
| AA Mutation | p.Arg397Trp(p.R397W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241014 |
| Start | 45902659:45902659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141639373 |
| CDS Mutation | c.892G>A |
| AA Mutation | p.Ala298Thr(p.A298T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241014 |
| Start | 45904090:45904090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1595G>A |
| AA Mutation | p.Arg532His(p.R532H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241014 |
| Start | 45902670:45902670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148774878 |
| CDS Mutation | c.903G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241014 |
| Start | 45902553:45902553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760993099 |
| CDS Mutation | c.786G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |