Primary Site >> Stomach Cancer
Gene >> MAZ
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322945 |
| Start | 29806823:29806823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.122C>G |
| AA Mutation | p.Pro41Arg(p.P41R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322945 |
| Start | 29807753:29807753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.968G>T |
| AA Mutation | p.Ser323Ile(p.S323I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322945 |
| Start | 29807795:29807795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1010A>G |
| AA Mutation | p.Tyr337Cys(p.Y337C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322945 |
| Start | 29807753:29807753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768483206 |
| CDS Mutation | c.968G>A |
| AA Mutation | p.Ser323Asn(p.S323N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322945 |
| Start | 29806730:29806730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.29T>C |
| AA Mutation | p.Leu10Pro(p.L10P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322945 |
| Start | 29806776:29806776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749236448 |
| CDS Mutation | c.75C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322945 |
| Start | 29808722:29808722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374491337 |
| CDS Mutation | c.1260C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322945 |
| Start | 29810120:29810120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1323G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322945 |
| Start | 29810120:29810120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370548510 |
| CDS Mutation | c.1323G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000322945 |
| Start | 29806733:29806733(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs767720617 |
| CDS Mutation | c.39delC |
| AA Mutation | p.Phe14SerfsTer15(p.F14Sfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000322945 |
| Start | 29806766:29806766(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.70delG |
| AA Mutation | p.Val24TrpfsTer5(p.V24Wfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000322945 |
| Start | 29806732:29806733(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs775841544 |
| CDS Mutation | c.39dupC |
| AA Mutation | p.Phe14LeufsTer34(p.F14Lfs*34) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000322945 |
| Start | 29807754:29807755(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.969_970insAGGAGTAAGATTTTCAGTAAA |
| AA Mutation | p.Ser323_Tyr324insArgSerLysIlePheSerLys(p.S323_Y324insRSKIFSK) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |