Primary Site >> Stomach Cancer
Gene >> FURIN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268171 |
| Start | 90880942:90880942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1694A>C |
| AA Mutation | p.Lys565Thr(p.K565T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268171 |
| Start | 90877559:90877559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.611C>T |
| AA Mutation | p.Ala204Val(p.A204V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268171 |
| Start | 90881840:90881840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2347G>A |
| AA Mutation | p.Glu783Lys(p.E783K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268171 |
| Start | 90878815:90878815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749858583 |
| CDS Mutation | c.892C>T |
| AA Mutation | p.Arg298Trp(p.R298W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268171 |
| Start | 90879687:90879687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1171C>T |
| AA Mutation | p.Arg391Trp(p.R391W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268171 |
| Start | 90878951:90878951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1028G>A |
| AA Mutation | p.Ser343Asn(p.S343N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268171 |
| Start | 90879977:90879977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1369G>A |
| AA Mutation | p.Glu457Lys(p.E457K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268171 |
| Start | 90880174:90880174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1457A>T |
| AA Mutation | p.His486Leu(p.H486L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268171 |
| Start | 90880211:90880211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1494T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268171 |
| Start | 90881827:90881827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753334944 |
| CDS Mutation | c.2334C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268171 |
| Start | 90881389:90881389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201838174 |
| CDS Mutation | c.1896C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268171 |
| Start | 90880964:90880964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1716C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268171 |
| Start | 90879964:90879964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375829786 |
| CDS Mutation | c.1356C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |