Primary Site >> Stomach Cancer
Gene >> BRSK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309383 |
| Start | 55304054:55304054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1291C>T |
| AA Mutation | p.Arg431Cys(p.R431C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309383 |
| Start | 55301627:55301627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.794T>C |
| AA Mutation | p.Met265Thr(p.M265T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000309383 |
| Start | 55305585:55305585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1889C>T |
| AA Mutation | p.Ser630Leu(p.S630L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309383 |
| Start | 55304827:55304827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1624G>A |
| AA Mutation | p.Gly542Ser(p.G542S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309383 |
| Start | 55311979:55311979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574851872 |
| CDS Mutation | c.2248C>T |
| AA Mutation | p.Arg750Cys(p.R750C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000309383 |
| Start | 55305585:55305585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1889C>G |
| AA Mutation | p.Ser630Trp(p.S630W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309383 |
| Start | 55289574:55289574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765382042 |
| CDS Mutation | c.412C>T |
| AA Mutation | p.Arg138Cys(p.R138C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309383 |
| Start | 55302744:55302744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.905G>A |
| AA Mutation | p.Arg302His(p.R302H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309383 |
| Start | 55301620:55301620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.787A>G |
| AA Mutation | p.Arg263Gly(p.R263G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309383 |
| Start | 55302818:55302818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.979G>T |
| AA Mutation | p.Gly327Cys(p.G327C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309383 |
| Start | 55301572:55301572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.739G>A |
| AA Mutation | p.Val247Ile(p.V247I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309383 |
| Start | 55289501:55289501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.339C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309383 |
| Start | 55301650:55301650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.817A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000309383 |
| Start | 55303668:55303668(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs746043904 |
| CDS Mutation | c.1135delC |
| AA Mutation | p.Arg379GlyfsTer9(p.R379Gfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |