Primary Site >> Stomach Cancer
Gene >> SERPINA5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329597 |
| Start | 94587443:94587443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.81G>A |
| AA Mutation | p.Met27Ile(p.M27I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329597 |
| Start | 94587478:94587478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.116C>T |
| AA Mutation | p.Thr39Met(p.T39M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329597 |
| Start | 94587403:94587403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.41C>T |
| AA Mutation | p.Pro14Leu(p.P14L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329597 |
| Start | 94590164:94590164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201469061 |
| CDS Mutation | c.743G>A |
| AA Mutation | p.Arg248Gln(p.R248Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329597 |
| Start | 94590133:94590133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.712C>A |
| AA Mutation | p.Arg238Ser(p.R238S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329597 |
| Start | 94592106:94592106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1088C>T |
| AA Mutation | p.Ala363Val(p.A363V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329597 |
| Start | 94592086:94592086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760259738 |
| CDS Mutation | c.1068C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329597 |
| Start | 94587404:94587404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.42T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000329597 |
| Start | 94587484:94587484(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.126delC |
| AA Mutation | p.Ser43AlafsTer28(p.S43Afs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |