Primary Site >> Stomach Cancer
Gene >> ANGPT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325203 |
| Start | 6513814:6513814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1063C>G |
| AA Mutation | p.Leu355Val(p.L355V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325203 |
| Start | 6532387:6532387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.389A>T |
| AA Mutation | p.Asn130Ile(p.N130I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325203 |
| Start | 6508991:6508991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1271G>T |
| AA Mutation | p.Ser424Ile(p.S424I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325203 |
| Start | 6562774:6562774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749213090 |
| CDS Mutation | c.161G>A |
| AA Mutation | p.Arg54His(p.R54H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325203 |
| Start | 6503181:6503181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1411G>A |
| AA Mutation | p.Gly471Ser(p.G471S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325203 |
| Start | 6514716:6514716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.993C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325203 |
| Start | 6513794:6513794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200777464 |
| CDS Mutation | c.1083G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325203 |
| Start | 6532413:6532413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144017946 |
| CDS Mutation | c.363G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325203 |
| Start | 6514713:6514713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764298644 |
| CDS Mutation | c.996C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |