Primary Site >> Stomach Cancer
Gene >> FBXO11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47819071:47819071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1805A>G |
| AA Mutation | p.Lys602Arg(p.K602R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47823191:47823191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1568A>G |
| AA Mutation | p.Asn523Ser(p.N523S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47808164:47808164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2738A>G |
| AA Mutation | p.Tyr913Cys(p.Y913C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47839475:47839475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.386A>G |
| AA Mutation | p.Asn129Ser(p.N129S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47808221:47808221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2681C>T |
| AA Mutation | p.Thr894Ile(p.T894I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47818999:47818999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1877G>A |
| AA Mutation | p.Ser626Asn(p.S626N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47810394:47810394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2260G>A |
| AA Mutation | p.Ala754Thr(p.A754T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47823288:47823288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1471A>G |
| AA Mutation | p.Thr491Ala(p.T491A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47808191:47808191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2711A>G |
| AA Mutation | p.Glu904Gly(p.E904G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47823176:47823176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1583T>C |
| AA Mutation | p.Val528Ala(p.V528A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403359 |
| Start | 47823147:47823147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1612A>G |
| AA Mutation | p.Ile538Val(p.I538V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000403359 |
| Start | 47822228:47822228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1692T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000403359 |
| Start | 47839693:47839693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773113676 |
| CDS Mutation | c.309A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000403359 |
| Start | 47808218:47808219(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2683_2684delCT |
| AA Mutation | p.Leu895ValfsTer2(p.L895Vfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000403359 |
| Start | 47819021:47819021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1855G>T |
| AA Mutation | p.Gly619Ter(p.G619*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000403359 |
| Start | 47832445:47832446(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1301dupC |
| AA Mutation | p.Gly435TrpfsTer5(p.G435Wfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000403359 |
| Start | 47839749:47839750(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.252dupT |
| AA Mutation | p.Met85TyrfsTer13(p.M85Yfs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000403359 |
| Start | 47809166:47809168(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2545_2547delGAT |
| AA Mutation | p.Asp849del(p.D849del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |