Primary Site >> Stomach Cancer
Gene >> PXN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228307 |
| Start | 120222898:120222898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.458A>T |
| AA Mutation | p.Asn153Ile(p.N153I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228307 |
| Start | 120213910:120213910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768579833 |
| CDS Mutation | c.1441C>T |
| AA Mutation | p.Arg481Trp(p.R481W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228307 |
| Start | 120213871:120213871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1480C>A |
| AA Mutation | p.Leu494Met(p.L494M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000228307 |
| Start | 120222944:120222944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.412C>A |
| AA Mutation | p.Leu138Met(p.L138M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228307 |
| Start | 120222996:120222996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.360C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000228307 |
| Start | 120214942:120214942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1161C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000228307 |
| Start | 120224233:120224233(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.158delC |
| AA Mutation | p.Pro53ArgfsTer14(p.P53Rfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000228307 |
| Start | 120224247:120224247(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758654594 |
| CDS Mutation | c.144delC |
| AA Mutation | p.Val49SerfsTer18(p.V49Sfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |