Primary Site >> Stomach Cancer
Gene >> KANK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 732452:732452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3080T>G |
| AA Mutation | p.Val1027Gly(p.V1027G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 711848:711848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139689422 |
| CDS Mutation | c.1082C>T |
| AA Mutation | p.Thr361Met(p.T361M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 742244:742244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369238209 |
| CDS Mutation | c.3736C>T |
| AA Mutation | p.Arg1246Trp(p.R1246W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 730125:730125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2773C>T |
| AA Mutation | p.Pro925Ser(p.P925S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 711872:711872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1106A>G |
| AA Mutation | p.Gln369Arg(p.Q369R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 712098:712098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1332G>T |
| AA Mutation | p.Met444Ile(p.M444I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 711335:711335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752973772 |
| CDS Mutation | c.569T>C |
| AA Mutation | p.Met190Thr(p.M190T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 711061:711061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.295G>A |
| AA Mutation | p.Asp99Asn(p.D99N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 710960:710960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.194A>C |
| AA Mutation | p.Lys65Thr(p.K65T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 712351:712351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1585A>C |
| AA Mutation | p.Ser529Arg(p.S529R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 711323:711323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.557G>A |
| AA Mutation | p.Ser186Asn(p.S186N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 713305:713305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2539G>A |
| AA Mutation | p.Glu847Lys(p.E847K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 732418:732418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3046A>C |
| AA Mutation | p.Ser1016Arg(p.S1016R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 712829:712829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146648084 |
| CDS Mutation | c.2063C>T |
| AA Mutation | p.Thr688Met(p.T688M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 712285:712285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1519G>A |
| AA Mutation | p.Ala507Thr(p.A507T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 711091:711091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.325G>A |
| AA Mutation | p.Ala109Thr(p.A109T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382297 |
| Start | 711849:711849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534950294 |
| CDS Mutation | c.1083G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382297 |
| Start | 712605:712605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1839C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382297 |
| Start | 744580:744580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3987C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382297 |
| Start | 732477:732477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569686873 |
| CDS Mutation | c.3105G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382297 |
| Start | 742369:742369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3861G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382297 |
| Start | 676999:676999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.27C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382297 |
| Start | 711135:711135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.369C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382297 |
| Start | 713157:713157(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2395delG |
| AA Mutation | p.Val799LeufsTer6(p.V799Lfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382297 |
| Start | 711074:711075(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.312dupC |
| AA Mutation | p.Asn105GlnfsTer47(p.N105Qfs*47) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000382297 |
| Start | 742406:742406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758108591 |
| CDS Mutation | c.3897+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |