Primary Site >> Stomach Cancer
Gene >> SERPING1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278407 |
| Start | 57606061:57606061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.737G>A |
| AA Mutation | p.Ser246Asn(p.S246N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000278407 |
| Start | 57600377:57600377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs281875170 |
| CDS Mutation | c.550G>A |
| AA Mutation | p.Gly184Arg(p.G184R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278407 |
| Start | 57614361:57614361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1283G>A |
| AA Mutation | p.Cys428Tyr(p.C428Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278407 |
| Start | 57606432:57606432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.914C>T |
| AA Mutation | p.Pro305Leu(p.P305L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278407 |
| Start | 57614370:57614370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1292C>A |
| AA Mutation | p.Thr431Lys(p.T431K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278407 |
| Start | 57602048:57602048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.564C>A |
| AA Mutation | p.Asn188Lys(p.N188K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278407 |
| Start | 57606435:57606435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.917A>C |
| AA Mutation | p.Lys306Thr(p.K306T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000278407 |
| Start | 57600293:57600293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139035354 |
| CDS Mutation | c.466G>A |
| AA Mutation | p.Ala156Thr(p.A156T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000278407 |
| Start | 57606122:57606122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375950989 |
| CDS Mutation | c.798G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |