Primary Site >> Stomach Cancer
Gene >> PSG2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406487 |
| Start | 43081052:43081052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377465339 |
| CDS Mutation | c.259C>G |
| AA Mutation | p.Gln87Glu(p.Q87E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406487 |
| Start | 43066579:43066579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.986T>C |
| AA Mutation | p.Leu329Pro(p.L329P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406487 |
| Start | 43075383:43075383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746390233 |
| CDS Mutation | c.680G>A |
| AA Mutation | p.Arg227His(p.R227H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406487 |
| Start | 43075429:43075429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.634G>A |
| AA Mutation | p.Ala212Thr(p.A212T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406487 |
| Start | 43071747:43071747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.917C>T |
| AA Mutation | p.Ser306Leu(p.S306L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406487 |
| Start | 43071744:43071744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.920C>G |
| AA Mutation | p.Ala307Gly(p.A307G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406487 |
| Start | 43071837:43071837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758633255 |
| CDS Mutation | c.827A>G |
| AA Mutation | p.Asn276Ser(p.N276S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406487 |
| Start | 43071875:43071875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761048790 |
| CDS Mutation | c.789G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406487 |
| Start | 43071878:43071878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200054104 |
| CDS Mutation | c.786C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406487 |
| Start | 43081038:43081038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.273T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406487 |
| Start | 43075541:43075541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146429644 |
| CDS Mutation | c.522G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000406487 |
| Start | 43075593:43075593(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.470delA |
| AA Mutation | p.Asn157ThrfsTer9(p.N157Tfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |