Primary Site >> Stomach Cancer
Gene >> POLR2F
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405557 |
| Start | 38025662:38025662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.377G>A |
| AA Mutation | p.Arg126His(p.R126H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442738 |
| Start | 37956783:37956783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550998177 |
| CDS Mutation | c.31G>A |
| AA Mutation | p.Asp11Asn(p.D11N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442738 |
| Start | 37956786:37956786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774791641 |
| CDS Mutation | c.34G>A |
| AA Mutation | p.Asp12Asn(p.D12N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442738 |
| Start | 37967637:37967637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.306C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442738 |
| Start | 37956785:37956785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747162109 |
| CDS Mutation | c.33C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000442738 |
| Start | 37959385:37959385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763157475 |
| CDS Mutation | c.130C>T |
| AA Mutation | p.Arg44Ter(p.R44*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |