Primary Site >> Stomach Cancer
Gene >> MAML3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000509479 |
| Start | 139720114:139720114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2626A>G |
| AA Mutation | p.Thr876Ala(p.T876A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000509479 |
| Start | 139720266:139720266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2474C>T |
| AA Mutation | p.Thr825Met(p.T825M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000509479 |
| Start | 139720269:139720269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747076119 |
| CDS Mutation | c.2471G>A |
| AA Mutation | p.Arg824Gln(p.R824Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000509479 |
| Start | 139890697:139890697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.739G>T |
| AA Mutation | p.Gly247Cys(p.G247C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000509479 |
| Start | 139890700:139890700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.736A>G |
| AA Mutation | p.Asn246Asp(p.N246D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000509479 |
| Start | 139719709:139719709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373700602 |
| CDS Mutation | c.3031G>A |
| AA Mutation | p.Val1011Met(p.V1011M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000509479 |
| Start | 139889560:139889560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1876A>G |
| AA Mutation | p.Asn626Asp(p.N626D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000509479 |
| Start | 139890446:139890446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761733625 |
| CDS Mutation | c.990C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000509479 |
| Start | 139890266:139890266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200009652 |
| CDS Mutation | c.1170G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000509479 |
| Start | 139719785:139719785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2955C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000509479 |
| Start | 139719365:139719365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748606151 |
| CDS Mutation | c.3375C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |