Primary Site >> Stomach Cancer
Gene >> PIK3C3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 41993306:41993306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.751G>A |
| AA Mutation | p.Glu251Lys(p.E251K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 42013530:42013530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1259A>C |
| AA Mutation | p.Lys420Thr(p.K420T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 41957583:41957583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756438946 |
| CDS Mutation | c.82G>A |
| AA Mutation | p.Gly28Arg(p.G28R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 42013489:42013489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1218A>C |
| AA Mutation | p.Glu406Asp(p.E406D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 42027456:42027456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1498G>A |
| AA Mutation | p.Glu500Lys(p.E500K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 42057922:42057922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2303G>A |
| AA Mutation | p.Arg768Gln(p.R768Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 42037777:42037777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1925G>A |
| AA Mutation | p.Arg642His(p.R642H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 42037726:42037726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141329274 |
| CDS Mutation | c.1874C>T |
| AA Mutation | p.Thr625Met(p.T625M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 42058030:42058030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756468687 |
| CDS Mutation | c.2411C>T |
| AA Mutation | p.Thr804Met(p.T804M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 42033841:42033841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1723G>A |
| AA Mutation | p.Ala575Thr(p.A575T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 42067469:42067469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2605G>C |
| AA Mutation | p.Ala869Pro(p.A869P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262039 |
| Start | 42038788:42038788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1976G>A |
| AA Mutation | p.Arg659Gln(p.R659Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262039 |
| Start | 41995955:41995955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762755261 |
| CDS Mutation | c.852C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262039 |
| Start | 42049598:42049598(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2260delA |
| AA Mutation | p.Thr754GlnfsTer7(p.T754Qfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262039 |
| Start | 42064825:42064825(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2522delA |
| AA Mutation | p.Lys841ArgfsTer8(p.K841Rfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000262039 |
| Start | 41990468:41990468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778354842 |
| CDS Mutation | c.628C>T |
| AA Mutation | p.Arg210Ter(p.R210*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |