Primary Site >> Stomach Cancer
Gene >> CFH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196747246:196747246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3629G>A |
| AA Mutation | p.Arg1210His(p.R1210H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196725124:196725124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1700G>T |
| AA Mutation | p.Arg567Ile(p.R567I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196725172:196725172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1748A>G |
| AA Mutation | p.Lys583Arg(p.K583R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196677571:196677571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.523C>T |
| AA Mutation | p.Arg175Trp(p.R175W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196737532:196737532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2654G>T |
| AA Mutation | p.Arg885Met(p.R885M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196747224:196747224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145347741 |
| CDS Mutation | c.3607C>T |
| AA Mutation | p.Arg1203Trp(p.R1203W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196673129:196673129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.210A>C |
| AA Mutation | p.Glu70Asp(p.E70D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196690211:196690211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1308G>C |
| AA Mutation | p.Trp436Cys(p.W436C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196679628:196679628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.625T>G |
| AA Mutation | p.Ser209Ala(p.S209A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367429 |
| Start | 196747113:196747113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3496C>A |
| AA Mutation | p.Pro1166Thr(p.P1166T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196673005:196673005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.86A>C |
| AA Mutation | p.Asn29Thr(p.N29T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196690227:196690227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1324T>C |
| AA Mutation | p.Cys442Arg(p.C442R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196679640:196679640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.637C>T |
| AA Mutation | p.Pro213Ser(p.P213S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196726580:196726580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760174473 |
| CDS Mutation | c.1984A>G |
| AA Mutation | p.Arg662Gly(p.R662G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196673060:196673060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.141G>T |
| AA Mutation | p.Gln47His(p.Q47H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196725177:196725177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1753G>A |
| AA Mutation | p.Asp585Asn(p.D585N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196689476:196689476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773509771 |
| CDS Mutation | c.1021C>T |
| AA Mutation | p.Arg341Cys(p.R341C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196740735:196740735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2899G>A |
| AA Mutation | p.Gly967Arg(p.G967R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196715709:196715709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1636A>C |
| AA Mutation | p.Ser546Arg(p.S546R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196726899:196726899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201360629 |
| CDS Mutation | c.2195C>T |
| AA Mutation | p.Thr732Met(p.T732M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196726529:196726529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1933A>G |
| AA Mutation | p.Thr645Ala(p.T645A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367429 |
| Start | 196726524:196726524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1928A>G |
| AA Mutation | p.Glu643Gly(p.E643G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367429 |
| Start | 196747283:196747283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3666A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367429 |
| Start | 196715645:196715645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1572A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367429 |
| Start | 196673897:196673897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148182625 |
| CDS Mutation | c.285T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367429 |
| Start | 196737628:196737629(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2753dupG |
| AA Mutation | p.Trp920MetfsTer8(p.W920Mfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000367429 |
| Start | 196740793:196740793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2956+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000367429 |
| Start | 196742053:196742053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3133+2T>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |