Primary Site >> Stomach Cancer
Gene >> CA10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285273 |
| Start | 52072354:52072354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.101C>A |
| AA Mutation | p.Ala34Glu(p.A34E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285273 |
| Start | 51931076:51931076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780948449 |
| CDS Mutation | c.193C>T |
| AA Mutation | p.Arg65Trp(p.R65W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285273 |
| Start | 51635972:51635972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.672A>C |
| AA Mutation | p.Glu224Asp(p.E224D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285273 |
| Start | 51633561:51633561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.879C>A |
| AA Mutation | p.Asn293Lys(p.N293K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285273 |
| Start | 51633562:51633562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.878A>C |
| AA Mutation | p.Asn293Thr(p.N293T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285273 |
| Start | 52072372:52072372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.83T>C |
| AA Mutation | p.Ile28Thr(p.I28T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285273 |
| Start | 51931012:51931012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148839711 |
| CDS Mutation | c.257G>A |
| AA Mutation | p.Arg86His(p.R86H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285273 |
| Start | 51633638:51633638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.802C>T |
| AA Mutation | p.Arg268Cys(p.R268C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285273 |
| Start | 52157738:52157738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.49G>A |
| AA Mutation | p.Val17Ile(p.V17I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285273 |
| Start | 51931074:51931074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.195G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285273 |
| Start | 51747669:51747669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760599695 |
| CDS Mutation | c.429G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |