Primary Site >> Stomach Cancer
Gene >> TPO
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1484602:1484602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1345A>T |
| AA Mutation | p.Thr449Ser(p.T449S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1433466:1433466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.208C>A |
| AA Mutation | p.Pro70Thr(p.P70T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1496137:1496137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201782331 |
| CDS Mutation | c.2155G>A |
| AA Mutation | p.Glu719Lys(p.E719K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1484707:1484707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1450G>A |
| AA Mutation | p.Val484Met(p.V484M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1503989:1503989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759194294 |
| CDS Mutation | c.2428G>A |
| AA Mutation | p.Ala810Thr(p.A810T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1493960:1493960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1927T>C |
| AA Mutation | p.Phe643Leu(p.F643L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1487824:1487824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1601G>A |
| AA Mutation | p.Gly534Asp(p.G534D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1456187:1456187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780371451 |
| CDS Mutation | c.724G>A |
| AA Mutation | p.Ala242Thr(p.A242T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1484734:1484734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778515113 |
| CDS Mutation | c.1477G>A |
| AA Mutation | p.Gly493Ser(p.G493S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1504038:1504038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748124213 |
| CDS Mutation | c.2477C>T |
| AA Mutation | p.Ala826Val(p.A826V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1504041:1504041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2480A>T |
| AA Mutation | p.Asp827Val(p.D827V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1496607:1496607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2228G>T |
| AA Mutation | p.Gly743Val(p.G743V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1503996:1503996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752390603 |
| CDS Mutation | c.2435C>T |
| AA Mutation | p.Ala812Val(p.A812V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1496075:1496075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2093A>C |
| AA Mutation | p.Asn698Thr(p.N698T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1496711:1496711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2332G>C |
| AA Mutation | p.Glu778Gln(p.E778Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1453713:1453713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150812908 |
| CDS Mutation | c.502G>A |
| AA Mutation | p.Ala168Thr(p.A168T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1423120:1423120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.170C>T |
| AA Mutation | p.Thr57Met(p.T57M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1493930:1493930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1897G>A |
| AA Mutation | p.Asp633Asn(p.D633N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1487950:1487950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764548001 |
| CDS Mutation | c.1727C>T |
| AA Mutation | p.Ala576Val(p.A576V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1540703:1540703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750068617 |
| CDS Mutation | c.2728G>A |
| AA Mutation | p.Ala910Thr(p.A910T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1540679:1540679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368181428 |
| CDS Mutation | c.2704G>A |
| AA Mutation | p.Val902Ile(p.V902I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1484849:1484849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560609999 |
| CDS Mutation | c.1592G>A |
| AA Mutation | p.Arg531His(p.R531H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329066 |
| Start | 1423113:1423113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.163T>C |
| AA Mutation | p.Tyr55His(p.Y55H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1540702:1540702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765076528 |
| CDS Mutation | c.2727C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1414427:1414427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.19C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1540693:1540693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149611408 |
| CDS Mutation | c.2718G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1433549:1433549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.291A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1487843:1487843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1620A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1484772:1484772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146768724 |
| CDS Mutation | c.1515C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1496722:1496722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2343T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1487963:1487963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1740G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1484721:1484721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202005839 |
| CDS Mutation | c.1464C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1493983:1493983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1950G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1484754:1484754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776864359 |
| CDS Mutation | c.1497G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1477205:1477205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.939G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1477244:1477244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145985334 |
| CDS Mutation | c.978G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329066 |
| Start | 1504036:1504036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375133048 |
| CDS Mutation | c.2475C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |