Primary Site >> Stomach Cancer
Gene >> PIK3CD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9718859:9718859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774975013 |
| CDS Mutation | c.1186G>A |
| AA Mutation | p.Ala396Thr(p.A396T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9721512:9721512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1880G>T |
| AA Mutation | p.Cys627Phe(p.C627F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9720151:9720151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373779625 |
| CDS Mutation | c.1379G>A |
| AA Mutation | p.Arg460His(p.R460H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9721152:9721152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1715C>A |
| AA Mutation | p.Pro572Gln(p.P572Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9721787:9721787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1982C>T |
| AA Mutation | p.Ala661Val(p.A661V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9720139:9720139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751570218 |
| CDS Mutation | c.1367C>T |
| AA Mutation | p.Thr456Met(p.T456M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9720177:9720177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1405G>A |
| AA Mutation | p.Ala469Thr(p.A469T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9721807:9721807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2002C>A |
| AA Mutation | p.Leu668Met(p.L668M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9710473:9710473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.18C>A |
| AA Mutation | p.Asp6Glu(p.D6E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9724845:9724845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761274254 |
| CDS Mutation | c.2906G>A |
| AA Mutation | p.Arg969His(p.R969H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377346 |
| Start | 9717022:9717022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.844A>G |
| AA Mutation | p.Ile282Val(p.I282V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377346 |
| Start | 9721222:9721222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375016049 |
| CDS Mutation | c.1785C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377346 |
| Start | 9718708:9718708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1035C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377346 |
| Start | 9721201:9721201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559170089 |
| CDS Mutation | c.1764C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377346 |
| Start | 9715889:9715889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377346 |
| Start | 9717056:9717056(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs754116182 |
| CDS Mutation | c.883delC |
| AA Mutation | p.Gln295ArgfsTer39(p.Q295Rfs*39) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |