Primary Site >> Stomach Cancer
Gene >> CFAP46
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132857658:132857658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5506G>A |
| AA Mutation | p.Ala1836Thr(p.A1836T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132941605:132941605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.292T>C |
| AA Mutation | p.Ser98Pro(p.S98P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132938728:132938728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.397T>C |
| AA Mutation | p.Ser133Pro(p.S133P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132808608:132808608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142644767 |
| CDS Mutation | c.7961C>T |
| AA Mutation | p.Ala2654Val(p.A2654V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132847011:132847011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6188C>T |
| AA Mutation | p.Ala2063Val(p.A2063V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132808599:132808599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766366866 |
| CDS Mutation | c.7970G>A |
| AA Mutation | p.Arg2657His(p.R2657H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132808525:132808525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769349617 |
| CDS Mutation | c.8044G>A |
| AA Mutation | p.Val2682Ile(p.V2682I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132847303:132847303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs541680936 |
| CDS Mutation | c.5971G>A |
| AA Mutation | p.Gly1991Ser(p.G1991S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132941707:132941707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376888644 |
| CDS Mutation | c.190G>A |
| AA Mutation | p.Val64Met(p.V64M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132814866:132814866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7166G>A |
| AA Mutation | p.Ser2389Asn(p.S2389N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132937051:132937051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665G>A |
| AA Mutation | p.Arg222His(p.R222H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132938604:132938604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs191258313 |
| CDS Mutation | c.521G>A |
| AA Mutation | p.Arg174His(p.R174H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132833441:132833441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7034T>C |
| AA Mutation | p.Val2345Ala(p.V2345A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368586 |
| Start | 132810451:132810451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143790683 |
| CDS Mutation | c.7622C>T |
| AA Mutation | p.Ala2541Val(p.A2541V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368586 |
| Start | 132833503:132833503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746429808 |
| CDS Mutation | c.6972C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368586 |
| Start | 132808499:132808499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187918823 |
| CDS Mutation | c.8070C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368586 |
| Start | 132812828:132812828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781237485 |
| CDS Mutation | c.7458G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368586 |
| Start | 132938642:132938642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181449154 |
| CDS Mutation | c.483C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368586 |
| Start | 132814734:132814734(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7201delC |
| AA Mutation | p.Arg2401GlyfsTer9(p.R2401Gfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368586 |
| Start | 132814721:132814721(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7214delC |
| AA Mutation | p.Pro2405LeufsTer5(p.P2405Lfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368586 |
| Start | 132938663:132938663(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.462delC |
| AA Mutation | p.Ser155AlafsTer6(p.S155Afs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |