Primary Site >> Stomach Cancer
Gene >> HYAL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357750 |
| Start | 50320213:50320213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.277G>A |
| AA Mutation | p.Gly93Arg(p.G93R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357750 |
| Start | 50319705:50319705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1050074 |
| CDS Mutation | c.785G>A |
| AA Mutation | p.Arg262His(p.R262H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357750 |
| Start | 50318286:50318286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1265A>G |
| AA Mutation | p.Gln422Arg(p.Q422R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357750 |
| Start | 50318398:50318398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1153A>G |
| AA Mutation | p.Thr385Ala(p.T385A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357750 |
| Start | 50320431:50320431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.59C>T |
| AA Mutation | p.Ala20Val(p.A20V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357750 |
| Start | 50318367:50318367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143678537 |
| CDS Mutation | c.1184G>A |
| AA Mutation | p.Arg395His(p.R395H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |