Primary Site >> Stomach Cancer
Gene >> MARVELD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325631 |
| Start | 69419413:69419413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756888886 |
| CDS Mutation | c.28C>T |
| AA Mutation | p.Arg10Trp(p.R10W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325631 |
| Start | 69420281:69420281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.896C>T |
| AA Mutation | p.Ala299Val(p.A299V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325631 |
| Start | 69419825:69419825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143318841 |
| CDS Mutation | c.440G>A |
| AA Mutation | p.Arg147Gln(p.R147Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325631 |
| Start | 69420277:69420277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.892G>A |
| AA Mutation | p.Val298Ile(p.V298I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325631 |
| Start | 69432603:69432603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1259A>G |
| AA Mutation | p.Lys420Arg(p.K420R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325631 |
| Start | 69420075:69420075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369204943 |
| CDS Mutation | c.690G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325631 |
| Start | 69432565:69432565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1221A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325631 |
| Start | 69419691:69419691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181575833 |
| CDS Mutation | c.306G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000325631 |
| Start | 69419530:69419530(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.149delC |
| AA Mutation | p.Pro50LeufsTer22(p.P50Lfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000325631 |
| Start | 69432628:69432628(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1289delC |
| AA Mutation | p.Pro430GlnfsTer9(p.P430Qfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000325631 |
| Start | 69440489:69440489(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs781701172 |
| CDS Mutation | c.1550delA |
| AA Mutation | p.Lys517ArgfsTer16(p.K517Rfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000325631 |
| Start | 69432986:69432986(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1399delT |
| AA Mutation | p.Ser467GlnfsTer14(p.S467Qfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |