Primary Site >> Stomach Cancer
Gene >> RAB11FIP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37872438:37872438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2364G>A |
| AA Mutation | p.Met788Ile(p.M788I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37874953:37874953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1184T>A |
| AA Mutation | p.Leu395Gln(p.L395Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37874793:37874793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1344G>T |
| AA Mutation | p.Lys448Asn(p.K448N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37871738:37871738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3064G>A |
| AA Mutation | p.Val1022Ile(p.V1022I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37877284:37877284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143926211 |
| CDS Mutation | c.639G>T |
| AA Mutation | p.Lys213Asn(p.K213N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37863002:37863002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754242991 |
| CDS Mutation | c.3745C>T |
| AA Mutation | p.Arg1249Cys(p.R1249C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37873159:37873159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560847102 |
| CDS Mutation | c.1643C>T |
| AA Mutation | p.Ala548Val(p.A548V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37871887:37871887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2915T>A |
| AA Mutation | p.Ile972Lys(p.I972K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37877147:37877147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.776A>T |
| AA Mutation | p.Glu259Val(p.E259V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37877163:37877163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.760C>G |
| AA Mutation | p.Gln254Glu(p.Q254E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37872865:37872865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1937A>C |
| AA Mutation | p.Asn646Thr(p.N646T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37872157:37872157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2645C>T |
| AA Mutation | p.Ala882Val(p.A882V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37899389:37899389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.53C>A |
| AA Mutation | p.Thr18Asn(p.T18N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330843 |
| Start | 37872487:37872487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371085767 |
| CDS Mutation | c.2315C>T |
| AA Mutation | p.Ala772Val(p.A772V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330843 |
| Start | 37872261:37872261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769711555 |
| CDS Mutation | c.2541C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330843 |
| Start | 37899427:37899427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330843 |
| Start | 37872483:37872483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2319C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330843 |
| Start | 37872951:37872951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552025766 |
| CDS Mutation | c.1851C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330843 |
| Start | 37874721:37874721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565580049 |
| CDS Mutation | c.1416G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330843 |
| Start | 37872252:37872252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142300397 |
| CDS Mutation | c.2550C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330843 |
| Start | 37872486:37872486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148197928 |
| CDS Mutation | c.2316G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000330843 |
| Start | 37899332:37899332(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs760708200 |
| CDS Mutation | c.110delG |
| AA Mutation | p.Gly37AlafsTer8(p.G37Afs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |