Primary Site >> Stomach Cancer
Gene >> PCSK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311106 |
| Start | 96398928:96398928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1539T>G |
| AA Mutation | p.Ile513Met(p.I513M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311106 |
| Start | 96410796:96410796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1073G>A |
| AA Mutation | p.Gly358Glu(p.G358E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311106 |
| Start | 96400089:96400089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1294G>T |
| AA Mutation | p.Gly432Cys(p.G432C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311106 |
| Start | 96432918:96432918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.125G>T |
| AA Mutation | p.Gly42Val(p.G42V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311106 |
| Start | 96412356:96412356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773564429 |
| CDS Mutation | c.844C>T |
| AA Mutation | p.Arg282Trp(p.R282W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311106 |
| Start | 96412325:96412325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.875T>C |
| AA Mutation | p.Val292Ala(p.V292A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311106 |
| Start | 96423419:96423419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.437T>G |
| AA Mutation | p.Leu146Arg(p.L146R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311106 |
| Start | 96393242:96393242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2021C>T |
| AA Mutation | p.Ala674Val(p.A674V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311106 |
| Start | 96410786:96410786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1083C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311106 |
| Start | 96410840:96410840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145132329 |
| CDS Mutation | c.1029C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311106 |
| Start | 96433010:96433010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.33T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311106 |
| Start | 96432932:96432932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199686748 |
| CDS Mutation | c.111G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |