Primary Site >> Stomach Cancer
Gene >> MAPK7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308406 |
| Start | 19381213:19381213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1004G>A |
| AA Mutation | p.Arg335His(p.R335H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308406 |
| Start | 19380757:19380757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.548T>C |
| AA Mutation | p.Leu183Pro(p.L183P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308406 |
| Start | 19381467:19381467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1258C>T |
| AA Mutation | p.Pro420Ser(p.P420S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308406 |
| Start | 19380880:19380880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.671C>T |
| AA Mutation | p.Thr224Met(p.T224M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308406 |
| Start | 19383137:19383137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2357G>A |
| AA Mutation | p.Gly786Asp(p.G786D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308406 |
| Start | 19379895:19379895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147142467 |
| CDS Mutation | c.346G>A |
| AA Mutation | p.Ala116Thr(p.A116T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308406 |
| Start | 19380877:19380877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.668C>T |
| AA Mutation | p.Ala223Val(p.A223V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308406 |
| Start | 19381119:19381119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758067983 |
| CDS Mutation | c.910C>T |
| AA Mutation | p.Arg304Cys(p.R304C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308406 |
| Start | 19380896:19380896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.687G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308406 |
| Start | 19381523:19381523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755519791 |
| CDS Mutation | c.1314G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308406 |
| Start | 19380983:19380983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.774G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308406 |
| Start | 19381265:19381265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777031914 |
| CDS Mutation | c.1056T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |