Primary Site >> Stomach Cancer
Gene >> PRF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70600815:70600815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.88G>C |
| AA Mutation | p.Glu30Gln(p.E30Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70598855:70598855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150628656 |
| CDS Mutation | c.866C>T |
| AA Mutation | p.Thr289Met(p.T289M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70598417:70598417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs28933376 |
| CDS Mutation | c.1304C>T |
| AA Mutation | p.Thr435Met(p.T435M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70598890:70598890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.831G>T |
| AA Mutation | p.Lys277Asn(p.K277N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70600527:70600527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34279237 |
| CDS Mutation | c.376C>T |
| AA Mutation | p.Arg126Cys(p.R126C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70600371:70600371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.532T>G |
| AA Mutation | p.Phe178Val(p.F178V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70599099:70599099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.622A>G |
| AA Mutation | p.Thr208Ala(p.T208A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70599018:70599018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.703G>A |
| AA Mutation | p.Ala235Thr(p.A235T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70598652:70598652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757636984 |
| CDS Mutation | c.1069C>T |
| AA Mutation | p.Arg357Trp(p.R357W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70600374:70600374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201468340 |
| CDS Mutation | c.529C>T |
| AA Mutation | p.Arg177Cys(p.R177C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70599026:70599026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747380397 |
| CDS Mutation | c.695G>A |
| AA Mutation | p.Arg232His(p.R232H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70600770:70600770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs578092914 |
| CDS Mutation | c.133G>A |
| AA Mutation | p.Gly45Arg(p.G45R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373209 |
| Start | 70598954:70598954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.767A>C |
| AA Mutation | p.Asp256Ala(p.D256A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373209 |
| Start | 70600384:70600384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112883709 |
| CDS Mutation | c.519G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373209 |
| Start | 70599006:70599006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.715C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373209 |
| Start | 70599106:70599106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141130900 |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373209 |
| Start | 70598433:70598433(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1288delG |
| AA Mutation | p.Asp430ThrfsTer10(p.D430Tfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373209 |
| Start | 70598293:70598293(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs748926167 |
| CDS Mutation | c.1428delG |
| AA Mutation | p.Leu478Ter(p.L478*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |