Primary Site >> Stomach Cancer
Gene >> PORCN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326194 |
| Start | 48512665:48512665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.632G>A |
| AA Mutation | p.Gly211Asp(p.G211D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326194 |
| Start | 48509914:48509914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.94C>T |
| AA Mutation | p.Leu32Phe(p.L32F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326194 |
| Start | 48516112:48516112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782631909 |
| CDS Mutation | c.1139G>A |
| AA Mutation | p.Arg380Gln(p.R380Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326194 |
| Start | 48516072:48516072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1099C>T |
| AA Mutation | p.Arg367Cys(p.R367C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326194 |
| Start | 48514326:48514326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.806C>T |
| AA Mutation | p.Ala269Val(p.A269V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326194 |
| Start | 48516111:48516111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782208997 |
| CDS Mutation | c.1138C>T |
| AA Mutation | p.Arg380Trp(p.R380W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326194 |
| Start | 48512445:48512445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781926599 |
| CDS Mutation | c.493A>G |
| AA Mutation | p.Ile165Val(p.I165V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |