Primary Site >> Stomach Cancer
Gene >> PRICKLE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42464929:42464929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1105G>A |
| AA Mutation | p.Asp369Asn(p.D369N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42466263:42466263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372213429 |
| CDS Mutation | c.706C>T |
| AA Mutation | p.Arg236Cys(p.R236C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42460353:42460353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750913400 |
| CDS Mutation | c.1952C>T |
| AA Mutation | p.Pro651Leu(p.P651L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42460468:42460468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1837C>T |
| AA Mutation | p.Pro613Ser(p.P613S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42465214:42465214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762434475 |
| CDS Mutation | c.820G>A |
| AA Mutation | p.Ala274Thr(p.A274T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42460327:42460327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143947284 |
| CDS Mutation | c.1978G>A |
| AA Mutation | p.Val660Ile(p.V660I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42460633:42460633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1672C>T |
| AA Mutation | p.Pro558Ser(p.P558S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42459954:42459954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2351C>A |
| AA Mutation | p.Pro784His(p.P784H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42465063:42465063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.971C>T |
| AA Mutation | p.Ser324Leu(p.S324L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42466283:42466283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.686G>T |
| AA Mutation | p.Arg229Met(p.R229M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42465012:42465012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577174749 |
| CDS Mutation | c.1022G>A |
| AA Mutation | p.Arg341Gln(p.R341Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42464454:42464454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1580T>G |
| AA Mutation | p.Leu527Arg(p.L527R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42470290:42470290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.202C>T |
| AA Mutation | p.Arg68Trp(p.R68W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42464913:42464913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1121A>G |
| AA Mutation | p.Lys374Arg(p.K374R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42464803:42464803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1231C>T |
| AA Mutation | p.His411Tyr(p.H411Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42460087:42460087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2218G>A |
| AA Mutation | p.Asp740Asn(p.D740N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42464787:42464787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151332996 |
| CDS Mutation | c.1247C>T |
| AA Mutation | p.Thr416Met(p.T416M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345127 |
| Start | 42466262:42466262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.707G>A |
| AA Mutation | p.Arg236His(p.R236H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345127 |
| Start | 42460040:42460040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148989635 |
| CDS Mutation | c.2265C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345127 |
| Start | 42464911:42464911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1123T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345127 |
| Start | 42460037:42460037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771279388 |
| CDS Mutation | c.2268C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345127 |
| Start | 42460328:42460328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1977C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345127 |
| Start | 42464975:42464975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769884613 |
| CDS Mutation | c.1059G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000345127 |
| Start | 42459825:42459825(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2480delA |
| AA Mutation | p.Asn827IlefsTer20(p.N827Ifs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000345127 |
| Start | 42465171:42465172(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.862_863delTT |
| AA Mutation | p.Leu288ValfsTer22(p.L288Vfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |