Primary Site >> Stomach Cancer
Gene >> MAGI3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000307546 |
| Start | 113653991:113653991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2602A>G |
| AA Mutation | p.Thr868Ala(p.T868A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000307546 |
| Start | 113642282:113642282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1732A>T |
| AA Mutation | p.Thr578Ser(p.T578S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000307546 |
| Start | 113659250:113659250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2800G>A |
| AA Mutation | p.Val934Ile(p.V934I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000307546 |
| Start | 113659178:113659178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2728T>C |
| AA Mutation | p.Ser910Pro(p.S910P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000307546 |
| Start | 113659220:113659220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2770A>G |
| AA Mutation | p.Lys924Glu(p.K924E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000307546 |
| Start | 113641971:113641971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1421T>C |
| AA Mutation | p.Val474Ala(p.V474A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000307546 |
| Start | 113683487:113683487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3919A>C |
| AA Mutation | p.Lys1307Gln(p.K1307Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000307546 |
| Start | 113585545:113585545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.712G>A |
| AA Mutation | p.Glu238Lys(p.E238K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000307546 |
| Start | 113683070:113683070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61751950 |
| CDS Mutation | c.3502C>T |
| AA Mutation | p.Pro1168Ser(p.P1168S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000307546 |
| Start | 113681244:113681244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3236T>C |
| AA Mutation | p.Ile1079Thr(p.I1079T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000307546 |
| Start | 113682922:113682922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767690442 |
| CDS Mutation | c.3354G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000307546 |
| Start | 113659216:113659216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2766G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000307546 |
| Start | 113643752:113643752(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1976delC |
| AA Mutation | p.Ser659TyrfsTer8(p.S659Yfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000307546 |
| Start | 113642424:113642424(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1877delA |
| AA Mutation | p.Asn626MetfsTer5(p.N626Mfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000307546 |
| Start | 113673385:113673385(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3114delG |
| AA Mutation | p.Lys1039ArgfsTer61(p.K1039Rfs*61) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000307546 |
| Start | 113682959:113682959(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3395delC |
| AA Mutation | p.Pro1132HisfsTer16(p.P1132Hfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000307546 |
| Start | 113590565:113590566(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.845_846insA |
| AA Mutation | p.Phe282LeufsTer2(p.F282Lfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000307546 |
| Start | 113683057:113683058(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3489_3490insTTAATATCCC |
| AA Mutation | p.Lys1164LeufsTer9(p.K1164Lfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |