Primary Site >> Stomach Cancer
Gene >> CFTR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000003084 |
| Start | 117540120:117540120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143486492 |
| CDS Mutation | c.890G>A |
| AA Mutation | p.Arg297Gln(p.R297Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000003084 |
| Start | 117530951:117530951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121909031 |
| CDS Mutation | c.326A>G |
| AA Mutation | p.Tyr109Cys(p.Y109C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000003084 |
| Start | 117611638:117611638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121909019 |
| CDS Mutation | c.3197G>A |
| AA Mutation | p.Arg1066His(p.R1066H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000003084 |
| Start | 117606740:117606740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2975T>C |
| AA Mutation | p.Phe992Ser(p.F992S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000003084 |
| Start | 117652858:117652858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3890C>G |
| AA Mutation | p.Ser1297Cys(p.S1297C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000003084 |
| Start | 117595017:117595017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2578A>C |
| AA Mutation | p.Ile860Leu(p.I860L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000003084 |
| Start | 117542032:117542032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768589673 |
| CDS Mutation | c.1133A>G |
| AA Mutation | p.Gln378Arg(p.Q378R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000003084 |
| Start | 117540321:117540321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1091C>G |
| AA Mutation | p.Ser364Cys(p.S364C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000003084 |
| Start | 117559549:117559549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397508214 |
| CDS Mutation | c.1478A>C |
| AA Mutation | p.Gln493Pro(p.Q493P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000003084 |
| Start | 117530900:117530900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.275A>T |
| AA Mutation | p.Glu92Val(p.E92V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000003084 |
| Start | 117592426:117592426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201888075 |
| CDS Mutation | c.2259C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000003084 |
| Start | 117591967:117591967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1800G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000003084 |
| Start | 117606720:117606720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2955C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000003084 |
| Start | 117627599:117627599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3546C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000003084 |
| Start | 117642527:117642527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1800129 |
| CDS Mutation | c.3807C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000003084 |
| Start | 117664711:117664712(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3988_3989delCA |
| AA Mutation | p.Gln1330ValfsTer6(p.Q1330Vfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000003084 |
| Start | 117592251:117592251(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2089delA |
| AA Mutation | p.Arg697GlyfsTer25(p.R697Gfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000003084 |
| Start | 117652852:117652852(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3889delT |
| AA Mutation | p.Ser1297LeufsTer31(p.S1297Lfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000003084 |
| Start | 117480138:117480138(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774973931 |
| CDS Mutation | c.50delT |
| AA Mutation | p.Phe17SerfsTer8(p.F17Sfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000003084 |
| Start | 117536649:117536649(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.850delA |
| AA Mutation | p.Met284Ter(p.M284*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000003084 |
| Start | 117592213:117592213(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs777301769 |
| CDS Mutation | c.2052delA |
| AA Mutation | p.Lys684AsnfsTer38(p.K684Nfs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000003084 |
| Start | 117592292:117592292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121908760 |
| CDS Mutation | c.2125C>T |
| AA Mutation | p.Arg709Ter(p.R709*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000003084 |
| Start | 117592457:117592457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121908810 |
| CDS Mutation | c.2290C>T |
| AA Mutation | p.Arg764Ter(p.R764*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000003084 |
| Start | 117592250:117592251(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2089dupA |
| AA Mutation | p.Arg697LysfsTer33(p.R697Kfs*33) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |