Primary Site >> Stomach Cancer
Gene >> SPINK5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256084 |
| Start | 148091191:148091191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.629G>C |
| AA Mutation | p.Arg210Pro(p.R210P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256084 |
| Start | 148070435:148070435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552548594 |
| CDS Mutation | c.194C>T |
| AA Mutation | p.Thr65Met(p.T65M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256084 |
| Start | 148114455:148114455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1981C>A |
| AA Mutation | p.His661Asn(p.H661N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256084 |
| Start | 148108766:148108766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1621G>A |
| AA Mutation | p.Glu541Lys(p.E541K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256084 |
| Start | 148100497:148100497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1136T>C |
| AA Mutation | p.Leu379Pro(p.L379P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256084 |
| Start | 148133801:148133801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3100C>T |
| AA Mutation | p.Arg1034Cys(p.R1034C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256084 |
| Start | 148094427:148094427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539094987 |
| CDS Mutation | c.740G>A |
| AA Mutation | p.Arg247His(p.R247H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256084 |
| Start | 148101388:148101388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1254A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256084 |
| Start | 148120059:148120059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767931984 |
| CDS Mutation | c.2364C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256084 |
| Start | 148111818:148111818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1743T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256084 |
| Start | 148101824:148101824(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs778763517 |
| CDS Mutation | c.1351delT |
| AA Mutation | p.Cys451AlafsTer53(p.C451Afs*53) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256084 |
| Start | 148094397:148094397(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs773514258 |
| CDS Mutation | c.715delT |
| AA Mutation | p.Cys239ValfsTer56(p.C239Vfs*56) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256084 |
| Start | 148099297:148099297(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1077delA |
| AA Mutation | p.Ala360GlnfsTer15(p.A360Qfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256084 |
| Start | 148086423:148086423(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.306delA |
| AA Mutation | p.Gly103GlufsTer43(p.G103Efs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256084 |
| Start | 148095876:148095877(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.859dupA |
| AA Mutation | p.Thr287AsnfsTer2(p.T287Nfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256084 |
| Start | 148094396:148094397(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.715dupT |
| AA Mutation | p.Cys239LeufsTer6(p.C239Lfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256084 |
| Start | 148101823:148101824(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs754893266 |
| CDS Mutation | c.1351dupT |
| AA Mutation | p.Cys451LeufsTer6(p.C451Lfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000256084 |
| Start | 148123962:148123962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2666+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |