Primary Site >> Stomach Cancer
Gene >> SERPINC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367698 |
| Start | 173909666:173909666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1039A>G |
| AA Mutation | p.Met347Val(p.M347V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367698 |
| Start | 173917235:173917235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.25G>T |
| AA Mutation | p.Val9Leu(p.V9L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367698 |
| Start | 173914663:173914663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.298G>T |
| AA Mutation | p.Asp100Tyr(p.D100Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367698 |
| Start | 173911932:173911932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs483352852 |
| CDS Mutation | c.491G>A |
| AA Mutation | p.Arg164Gln(p.R164Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367698 |
| Start | 173911890:173911890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.533T>G |
| AA Mutation | p.Leu178Arg(p.L178R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367698 |
| Start | 173907454:173907454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1214T>G |
| AA Mutation | p.Leu405Arg(p.L405R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367698 |
| Start | 173914742:173914742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746429528 |
| CDS Mutation | c.219G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |