Primary Site >> Stomach Cancer
Gene >> TRAPPC9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140450874:140450874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.500C>G |
| AA Mutation | p.Ala167Gly(p.A167G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140451367:140451367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs76033442 |
| CDS Mutation | c.7G>A |
| AA Mutation | p.Val3Ile(p.V3I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140283898:140283898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2105C>T |
| AA Mutation | p.Ser702Phe(p.S702F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140371089:140371089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1226G>A |
| AA Mutation | p.Arg409His(p.R409H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140371087:140371087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1228G>A |
| AA Mutation | p.Val410Met(p.V410M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140287670:140287670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1919C>T |
| AA Mutation | p.Ser640Phe(p.S640F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140451175:140451175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748601792 |
| CDS Mutation | c.199G>A |
| AA Mutation | p.Glu67Lys(p.E67K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140300505:140300505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750502015 |
| CDS Mutation | c.1732G>A |
| AA Mutation | p.Ala578Thr(p.A578T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140397736:140397736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1018G>C |
| AA Mutation | p.Ala340Pro(p.A340P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140451150:140451150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757282308 |
| CDS Mutation | c.224G>A |
| AA Mutation | p.Arg75His(p.R75H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140450988:140450988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.386G>A |
| AA Mutation | p.Arg129His(p.R129H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140371111:140371111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374409751 |
| CDS Mutation | c.1204C>T |
| AA Mutation | p.Arg402Cys(p.R402C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140311306:140311306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148453804 |
| CDS Mutation | c.1564G>A |
| AA Mutation | p.Ala522Thr(p.A522T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438773 |
| Start | 140371054:140371054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1261G>A |
| AA Mutation | p.Ala421Thr(p.A421T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438773 |
| Start | 140439158:140439158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202136646 |
| CDS Mutation | c.624C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438773 |
| Start | 140451152:140451152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766899177 |
| CDS Mutation | c.222C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438773 |
| Start | 140252811:140252811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2397C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438773 |
| Start | 140291065:140291065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1782T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438773 |
| Start | 140451368:140451368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565904872 |
| CDS Mutation | c.6C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438773 |
| Start | 140311292:140311292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1578C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438773 |
| Start | 140024056:140024056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2580C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438773 |
| Start | 139910258:139910258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754079193 |
| CDS Mutation | c.2853G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438773 |
| Start | 139732045:139732045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759408922 |
| CDS Mutation | c.3213C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438773 |
| Start | 140283966:140283966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371880751 |
| CDS Mutation | c.2037G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |