Primary Site >> Stomach Cancer
Gene >> CASZ1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10655705:10655705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150917673 |
| CDS Mutation | c.1609G>A |
| AA Mutation | p.Val537Ile(p.V537I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10642883:10642883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4138G>A |
| AA Mutation | p.Val1380Met(p.V1380M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10660341:10660341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.701C>T |
| AA Mutation | p.Ala234Val(p.A234V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10639976:10639976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772938935 |
| CDS Mutation | c.4246C>T |
| AA Mutation | p.Arg1416Trp(p.R1416W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10653890:10653890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2167G>T |
| AA Mutation | p.Asp723Tyr(p.D723Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10640018:10640018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772002077 |
| CDS Mutation | c.4204C>T |
| AA Mutation | p.Arg1402Cys(p.R1402C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10660339:10660339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754266033 |
| CDS Mutation | c.703C>T |
| AA Mutation | p.Arg235Trp(p.R235W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10653626:10653626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2431A>G |
| AA Mutation | p.Thr811Ala(p.T811A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10655792:10655792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1522G>T |
| AA Mutation | p.Val508Leu(p.V508L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10653974:10653974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2083C>T |
| AA Mutation | p.Arg695Trp(p.R695W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10655722:10655722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751917839 |
| CDS Mutation | c.1592C>T |
| AA Mutation | p.Pro531Leu(p.P531L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10659952:10659952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761216432 |
| CDS Mutation | c.1090G>A |
| AA Mutation | p.Ala364Thr(p.A364T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10647988:10647988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201167368 |
| CDS Mutation | c.3310G>A |
| AA Mutation | p.Ala1104Thr(p.A1104T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10659853:10659853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754239516 |
| CDS Mutation | c.1189C>A |
| AA Mutation | p.Pro397Thr(p.P397T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10647844:10647844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763703517 |
| CDS Mutation | c.3454G>A |
| AA Mutation | p.Ala1152Thr(p.A1152T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10639188:10639188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5034G>C |
| AA Mutation | p.Glu1678Asp(p.E1678D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10642996:10642996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4025C>A |
| AA Mutation | p.Pro1342His(p.P1342H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10654494:10654494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1763G>A |
| AA Mutation | p.Arg588His(p.R588H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10643216:10643216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780053498 |
| CDS Mutation | c.3964C>T |
| AA Mutation | p.Arg1322Trp(p.R1322W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10653754:10653754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2303C>T |
| AA Mutation | p.Pro768Leu(p.P768L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10646313:10646313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769502938 |
| CDS Mutation | c.3511G>A |
| AA Mutation | p.Ala1171Thr(p.A1171T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10639977:10639977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4245G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10639494:10639494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4728G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10660511:10660511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.531C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10654017:10654017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2040C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10644966:10644966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3819A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10653942:10653942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184103932 |
| CDS Mutation | c.2115G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10665183:10665183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.405C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10639560:10639560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4662C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10646239:10646239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751539348 |
| CDS Mutation | c.3585G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10660055:10660055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377360245 |
| CDS Mutation | c.987C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10653801:10653801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2256T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10639557:10639557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4665C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10665531:10665531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.57C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10653480:10653480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200262732 |
| CDS Mutation | c.2577C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10658549:10658549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151200081 |
| CDS Mutation | c.1368C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10665365:10665365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.223C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10659872:10659872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530829402 |
| CDS Mutation | c.1170G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10660220:10660220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.822C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377022 |
| Start | 10647956:10647956(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3342delC |
| AA Mutation | p.Thr1115ProfsTer35(p.T1115Pfs*35) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377022 |
| Start | 10665356:10665356(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.232delC |
| AA Mutation | p.Arg78AlafsTer10(p.R78Afs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000377022 |
| Start | 10654592:10654592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1666-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000377022 |
| Start | 10639964:10639965(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.4255_4257dupGCG |
| AA Mutation | p.Ala1419dup(p.A1419dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |