Primary Site >> Stomach Cancer
Gene >> NAPSA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253719 |
| Start | 50361697:50361697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746693112 |
| CDS Mutation | c.434G>A |
| AA Mutation | p.Arg145Gln(p.R145Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253719 |
| Start | 50361107:50361107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141372464 |
| CDS Mutation | c.502G>A |
| AA Mutation | p.Gly168Arg(p.G168R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253719 |
| Start | 50362249:50362249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.148C>A |
| AA Mutation | p.Pro50Thr(p.P50T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253719 |
| Start | 50360993:50360993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.616C>G |
| AA Mutation | p.Leu206Val(p.L206V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253719 |
| Start | 50359589:50359589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.850A>G |
| AA Mutation | p.Thr284Ala(p.T284A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253719 |
| Start | 50359074:50359074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372982608 |
| CDS Mutation | c.972C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253719 |
| Start | 50359050:50359050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.996G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253719 |
| Start | 50361075:50361075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775815223 |
| CDS Mutation | c.534C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253719 |
| Start | 50358604:50358604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1212C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253719 |
| Start | 50365547:50365547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.75A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253719 |
| Start | 50360995:50360995(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.614delT |
| AA Mutation | p.Val205AspfsTer61(p.V205Dfs*61) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253719 |
| Start | 50359048:50359049(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs568951683 |
| CDS Mutation | c.997dupG |
| AA Mutation | p.Val333GlyfsTer4(p.V333Gfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |