Primary Site >> Stomach Cancer
Gene >> IL21R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337929 |
| Start | 27430076:27430076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767011874 |
| CDS Mutation | c.5C>T |
| AA Mutation | p.Pro2Leu(p.P2L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337929 |
| Start | 27437492:27437492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.157G>A |
| AA Mutation | p.Asp53Asn(p.D53N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337929 |
| Start | 27444635:27444635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767388017 |
| CDS Mutation | c.601C>T |
| AA Mutation | p.Arg201Trp(p.R201W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337929 |
| Start | 27434361:27434361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149169230 |
| CDS Mutation | c.64G>A |
| AA Mutation | p.Asp22Asn(p.D22N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000337929 |
| Start | 27445276:27445276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.785G>A |
| AA Mutation | p.Arg262Lys(p.R262K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337929 |
| Start | 27449203:27449203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1537G>A |
| AA Mutation | p.Glu513Lys(p.E513K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337929 |
| Start | 27443025:27443025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746751826 |
| CDS Mutation | c.416G>A |
| AA Mutation | p.Arg139His(p.R139H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337929 |
| Start | 27448988:27448988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1322C>T |
| AA Mutation | p.Pro441Leu(p.P441L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337929 |
| Start | 27449069:27449069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779279193 |
| CDS Mutation | c.1403G>A |
| AA Mutation | p.Arg468Gln(p.R468Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337929 |
| Start | 27448840:27448840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1174T>G |
| AA Mutation | p.Cys392Gly(p.C392G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337929 |
| Start | 27437545:27437545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751906044 |
| CDS Mutation | c.210G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337929 |
| Start | 27442984:27442984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573659552 |
| CDS Mutation | c.375C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337929 |
| Start | 27442969:27442969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141558701 |
| CDS Mutation | c.360G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337929 |
| Start | 27430077:27430077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |