Primary Site >> Stomach Cancer
Gene >> MAP3K19
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375845 |
| Start | 134980978:134980978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3763T>C |
| AA Mutation | p.Cys1255Arg(p.C1255R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375845 |
| Start | 134980908:134980908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3833A>G |
| AA Mutation | p.Tyr1278Cys(p.Y1278C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375845 |
| Start | 134998806:134998806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.506A>G |
| AA Mutation | p.Asn169Ser(p.N169S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375845 |
| Start | 134987011:134987011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1861C>T |
| AA Mutation | p.Pro621Ser(p.P621S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375845 |
| Start | 134987493:134987493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1379G>A |
| AA Mutation | p.Ser460Asn(p.S460N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375845 |
| Start | 134986971:134986971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200710231 |
| CDS Mutation | c.1901C>T |
| AA Mutation | p.Pro634Leu(p.P634L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375845 |
| Start | 134980961:134980961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3780G>T |
| AA Mutation | p.Met1260Ile(p.M1260I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375845 |
| Start | 134981272:134981272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372912449 |
| CDS Mutation | c.3469C>T |
| AA Mutation | p.Pro1157Ser(p.P1157S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375845 |
| Start | 134981317:134981317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3424T>C |
| AA Mutation | p.Phe1142Leu(p.F1142L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375845 |
| Start | 134981335:134981335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3406G>A |
| AA Mutation | p.Val1136Met(p.V1136M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375845 |
| Start | 134981105:134981105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3636C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375845 |
| Start | 134987489:134987489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1383C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375845 |
| Start | 134988059:134988059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772166646 |
| CDS Mutation | c.813G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |