Primary Site >> Stomach Cancer
Gene >> MGAT3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341184 |
| Start | 39488540:39488540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1193G>A |
| AA Mutation | p.Arg398His(p.R398H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341184 |
| Start | 39487690:39487690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.343G>A |
| AA Mutation | p.Gly115Ser(p.G115S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341184 |
| Start | 39488479:39488479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1132G>A |
| AA Mutation | p.Gly378Ser(p.G378S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341184 |
| Start | 39487961:39487961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.614C>T |
| AA Mutation | p.Pro205Leu(p.P205L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341184 |
| Start | 39487966:39487966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.619C>A |
| AA Mutation | p.Arg207Ser(p.R207S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341184 |
| Start | 39488026:39488026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.679G>A |
| AA Mutation | p.Glu227Lys(p.E227K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341184 |
| Start | 39487361:39487361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14G>A |
| AA Mutation | p.Arg5His(p.R5H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341184 |
| Start | 39488061:39488061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.714C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341184 |
| Start | 39488001:39488001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.654C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341184 |
| Start | 39488751:39488751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758299553 |
| CDS Mutation | c.1404G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341184 |
| Start | 39488745:39488745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1398C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341184 |
| Start | 39488322:39488322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371459758 |
| CDS Mutation | c.975C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341184 |
| Start | 39487512:39487512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143400156 |
| CDS Mutation | c.165G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000341184 |
| Start | 39487366:39487366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.19A>T |
| AA Mutation | p.Lys7Ter(p.K7*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |