Primary Site >> Stomach Cancer
Gene >> SREBF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17817008:17817008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766878437 |
| CDS Mutation | c.1735G>A |
| AA Mutation | p.Ala579Thr(p.A579T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17817781:17817781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1319C>A |
| AA Mutation | p.Pro440His(p.P440H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17816982:17816982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1761G>C |
| AA Mutation | p.Lys587Asn(p.K587N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17816215:17816215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2206T>A |
| AA Mutation | p.Phe736Ile(p.F736I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17817125:17817125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1618T>C |
| AA Mutation | p.Trp540Arg(p.W540R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17817739:17817739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1361G>A |
| AA Mutation | p.Gly454Asp(p.G454D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17819074:17819074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1007G>A |
| AA Mutation | p.Arg336His(p.R336H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17820284:17820284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.329A>G |
| AA Mutation | p.Tyr110Cys(p.Y110C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17819119:17819119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962G>A |
| AA Mutation | p.Arg321His(p.R321H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17814687:17814687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529460681 |
| CDS Mutation | c.2663G>A |
| AA Mutation | p.Arg888Gln(p.R888Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261646 |
| Start | 17819557:17819557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.692C>T |
| AA Mutation | p.Ser231Leu(p.S231L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261646 |
| Start | 17817386:17817386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781342104 |
| CDS Mutation | c.1476G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261646 |
| Start | 17819670:17819670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775151936 |
| CDS Mutation | c.579G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261646 |
| Start | 17820271:17820271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762042920 |
| CDS Mutation | c.342C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261646 |
| Start | 17820280:17820280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375059574 |
| CDS Mutation | c.333G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261646 |
| Start | 17817750:17817750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766029447 |
| CDS Mutation | c.1350C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261646 |
| Start | 17818306:17818309(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1134_1137delGAAA |
| AA Mutation | p.Gln378HisfsTer7(p.Q378Hfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261646 |
| Start | 17817780:17817780(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1320delC |
| AA Mutation | p.Leu441CysfsTer257(p.L441Cfs*257) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |