Primary Site >> Stomach Cancer
Gene >> NT5C1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18584588:18584588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761245915 |
| CDS Mutation | c.829G>A |
| AA Mutation | p.Asp277Asn(p.D277N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18584194:18584194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.965A>G |
| AA Mutation | p.Asp322Gly(p.D322G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18586306:18586306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.386C>A |
| AA Mutation | p.Ser129Tyr(p.S129Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18584734:18584734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.683G>A |
| AA Mutation | p.Arg228Gln(p.R228Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18563990:18563990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777926079 |
| CDS Mutation | c.1639C>T |
| AA Mutation | p.Arg547Cys(p.R547C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000359846 |
| Start | 18582996:18582996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1073C>T |
| AA Mutation | p.Ala358Val(p.A358V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18584539:18584539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.878A>G |
| AA Mutation | p.Asn293Ser(p.N293S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18584605:18584605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812A>G |
| AA Mutation | p.Gln271Arg(p.Q271R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18584807:18584807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753832651 |
| CDS Mutation | c.610C>T |
| AA Mutation | p.Arg204Trp(p.R204W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18586369:18586369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142174343 |
| CDS Mutation | c.323G>A |
| AA Mutation | p.Arg108Gln(p.R108Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18584671:18584671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.746G>A |
| AA Mutation | p.Arg249His(p.R249H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18576305:18576305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201567504 |
| CDS Mutation | c.1388G>A |
| AA Mutation | p.Arg463His(p.R463H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359846 |
| Start | 18582895:18582895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183534911 |
| CDS Mutation | c.1174C>T |
| AA Mutation | p.Arg392Trp(p.R392W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |