Primary Site >> Stomach Cancer
Gene >> PRSS55
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328655 |
| Start | 10525712:10525712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.127C>T |
| AA Mutation | p.Pro43Ser(p.P43S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328655 |
| Start | 10538702:10538702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.968C>T |
| AA Mutation | p.Pro323Leu(p.P323L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328655 |
| Start | 10531438:10531438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.491C>T |
| AA Mutation | p.Ser164Leu(p.S164L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328655 |
| Start | 10531507:10531507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141913017 |
| CDS Mutation | c.560G>A |
| AA Mutation | p.Arg187His(p.R187H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328655 |
| Start | 10531414:10531414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.467A>G |
| AA Mutation | p.Asp156Gly(p.D156G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328655 |
| Start | 10538556:10538556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753600571 |
| CDS Mutation | c.822G>T |
| AA Mutation | p.Lys274Asn(p.K274N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328655 |
| Start | 10525647:10525647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148969594 |
| CDS Mutation | c.62G>A |
| AA Mutation | p.Arg21Gln(p.R21Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328655 |
| Start | 10531328:10531328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771081101 |
| CDS Mutation | c.381C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328655 |
| Start | 10531508:10531508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377217136 |
| CDS Mutation | c.561C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328655 |
| Start | 10538770:10538770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1036T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328655 |
| Start | 10525639:10525639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759945447 |
| CDS Mutation | c.54C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328655 |
| Start | 10538529:10538529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.795C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328655 |
| Start | 10529688:10529688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750765458 |
| CDS Mutation | c.336C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |