Primary Site >> Stomach Cancer
Gene >> NPNT
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000379987 |
| Start | 105942702:105942702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1159A>G |
| AA Mutation | p.Ile387Val(p.I387V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379987 |
| Start | 105942498:105942498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.955A>G |
| AA Mutation | p.Thr319Ala(p.T319A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379987 |
| Start | 105927375:105927375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.212G>A |
| AA Mutation | p.Gly71Glu(p.G71E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379987 |
| Start | 105940129:105940129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.560T>C |
| AA Mutation | p.Val187Ala(p.V187A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379987 |
| Start | 105967242:105967242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1400G>A |
| AA Mutation | p.Arg467His(p.R467H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379987 |
| Start | 105940607:105940607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.734G>A |
| AA Mutation | p.Gly245Glu(p.G245E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379987 |
| Start | 105958482:105958482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1171C>A |
| AA Mutation | p.Pro391Thr(p.P391T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000379987 |
| Start | 105898001:105898001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.172C>T |
| AA Mutation | p.Pro58Ser(p.P58S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379987 |
| Start | 105967223:105967223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1381C>T |
| AA Mutation | p.Pro461Ser(p.P461S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379987 |
| Start | 105940572:105940572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777864239 |
| CDS Mutation | c.699C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000379987 |
| Start | 105927412:105927412(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs779447711 |
| CDS Mutation | c.253delA |
| AA Mutation | p.Thr85ProfsTer6(p.T85Pfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000379987 |
| Start | 105927430:105927430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758923086 |
| CDS Mutation | c.265+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |