Primary Site >> Stomach Cancer
Gene >> CASP8AP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89869016:89869016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5726C>T |
| AA Mutation | p.Thr1909Ile(p.T1909I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89866384:89866384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3094C>T |
| AA Mutation | p.Pro1032Ser(p.P1032S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89862415:89862415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773140007 |
| CDS Mutation | c.706G>A |
| AA Mutation | p.Glu236Lys(p.E236K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89864188:89864188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2479G>A |
| AA Mutation | p.Ala827Thr(p.A827T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89867711:89867711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4421G>A |
| AA Mutation | p.Ser1474Asn(p.S1474N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89868662:89868662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5372A>T |
| AA Mutation | p.Glu1791Val(p.E1791V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89868613:89868613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5323A>G |
| AA Mutation | p.Lys1775Glu(p.K1775E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89868755:89868755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749146163 |
| CDS Mutation | c.5465A>G |
| AA Mutation | p.Asn1822Ser(p.N1822S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89862658:89862658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761188688 |
| CDS Mutation | c.949C>T |
| AA Mutation | p.Arg317Cys(p.R317C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89862724:89862724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1015A>C |
| AA Mutation | p.Ser339Arg(p.S339R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89867143:89867143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3853C>A |
| AA Mutation | p.Pro1285Thr(p.P1285T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89863061:89863061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202104748 |
| CDS Mutation | c.1352T>C |
| AA Mutation | p.Val451Ala(p.V451A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000551025 |
| Start | 89862374:89862374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.665G>T |
| AA Mutation | p.Cys222Phe(p.C222F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000551025 |
| Start | 89862414:89862414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777103420 |
| CDS Mutation | c.705C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000551025 |
| Start | 89863281:89863281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1572C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000551025 |
| Start | 89867343:89867343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147437828 |
| CDS Mutation | c.4053C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000551025 |
| Start | 89867292:89867292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756620482 |
| CDS Mutation | c.4002T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000551025 |
| Start | 89864109:89864109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767072178 |
| CDS Mutation | c.2400G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000551025 |
| Start | 89868231:89868231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4941T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000551025 |
| Start | 89866672:89866672(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774338802 |
| CDS Mutation | c.3390delA |
| AA Mutation | p.Lys1130AsnfsTer6(p.K1130Nfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000551025 |
| Start | 89868829:89868829(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5544delA |
| AA Mutation | p.Lys1848AsnfsTer8(p.K1848Nfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000551025 |
| Start | 89862439:89862439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.730A>T |
| AA Mutation | p.Arg244Ter(p.R244*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000551025 |
| Start | 89869034:89869035(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.5750dupA |
| AA Mutation | p.Asn1917LysfsTer4(p.N1917Kfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |