Primary Site >> Stomach Cancer
Gene >> MADD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47276849:47276849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1081G>A |
| AA Mutation | p.Ala361Thr(p.A361T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47315273:47315273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4323G>T |
| AA Mutation | p.Gln1441His(p.Q1441H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47290736:47290736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752053057 |
| CDS Mutation | c.3281G>A |
| AA Mutation | p.Arg1094Gln(p.R1094Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47289949:47289949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774124659 |
| CDS Mutation | c.2899C>T |
| AA Mutation | p.Arg967Cys(p.R967C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47274675:47274675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.175G>A |
| AA Mutation | p.Glu59Lys(p.E59K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47286444:47286444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144471266 |
| CDS Mutation | c.2563C>T |
| AA Mutation | p.Arg855Trp(p.R855W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47309322:47309322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3973G>A |
| AA Mutation | p.Glu1325Lys(p.E1325K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47285503:47285503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2464G>A |
| AA Mutation | p.Ala822Thr(p.A822T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47274637:47274637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.137T>G |
| AA Mutation | p.Phe46Cys(p.F46C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47275055:47275055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.555C>G |
| AA Mutation | p.Phe185Leu(p.F185L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47295921:47295921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3625C>A |
| AA Mutation | p.Leu1209Ile(p.L1209I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47281590:47281590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1306A>T |
| AA Mutation | p.Ser436Cys(p.S436C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47324317:47324317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4595G>A |
| AA Mutation | p.Arg1532Gln(p.R1532Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47284275:47284275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1960A>G |
| AA Mutation | p.Thr654Ala(p.T654A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47329067:47329067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140803760 |
| CDS Mutation | c.4861G>A |
| AA Mutation | p.Val1621Ile(p.V1621I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311027 |
| Start | 47282409:47282409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770084863 |
| CDS Mutation | c.1498G>A |
| AA Mutation | p.Ala500Thr(p.A500T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311027 |
| Start | 47285129:47285129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201805956 |
| CDS Mutation | c.2346G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311027 |
| Start | 47274581:47274581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746888060 |
| CDS Mutation | c.81C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311027 |
| Start | 47286515:47286515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2634G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311027 |
| Start | 47289440:47289440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2763C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000311027 |
| Start | 47290685:47290685(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3235delG |
| AA Mutation | p.Asp1079ThrfsTer8(p.D1079Tfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000311027 |
| Start | 47326780:47326780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267602902 |
| CDS Mutation | c.4765C>T |
| AA Mutation | p.Arg1589Ter(p.R1589*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000311027 |
| Start | 47274609:47274609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.109C>T |
| AA Mutation | p.Arg37Ter(p.R37*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000311027 |
| Start | 47308624:47308624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3793G>T |
| AA Mutation | p.Glu1265Ter(p.E1265*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |