Primary Site >> Stomach Cancer
Gene >> HHLA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357759 |
| Start | 108353673:108353673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771206254 |
| CDS Mutation | c.311C>T |
| AA Mutation | p.Ala104Val(p.A104V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357759 |
| Start | 108353708:108353708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367817011 |
| CDS Mutation | c.346G>A |
| AA Mutation | p.Glu116Lys(p.E116K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357759 |
| Start | 108357907:108357907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.749T>G |
| AA Mutation | p.Phe250Cys(p.F250C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357759 |
| Start | 108353670:108353670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.308A>G |
| AA Mutation | p.Asn103Ser(p.N103S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357759 |
| Start | 108355267:108355267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752698352 |
| CDS Mutation | c.571G>A |
| AA Mutation | p.Asp191Asn(p.D191N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357759 |
| Start | 108353476:108353476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746832212 |
| CDS Mutation | c.114C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |