Primary Site >> Stomach Cancer
Gene >> PANX2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177589:50177589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371220405 |
| CDS Mutation | c.877G>A |
| AA Mutation | p.Val293Met(p.V293M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177361:50177361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649C>T |
| AA Mutation | p.Arg217Cys(p.R217C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177482:50177482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.770T>C |
| AA Mutation | p.Phe257Ser(p.F257S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50179185:50179185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1942G>A |
| AA Mutation | p.Val648Met(p.V648M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50176987:50176987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768497136 |
| CDS Mutation | c.275C>T |
| AA Mutation | p.Ala92Val(p.A92V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50170953:50170953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.223G>A |
| AA Mutation | p.Ala75Thr(p.A75T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177713:50177713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139331786 |
| CDS Mutation | c.1001G>A |
| AA Mutation | p.Arg334Gln(p.R334Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177524:50177524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812C>T |
| AA Mutation | p.Ala271Val(p.A271V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177776:50177776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1064G>A |
| AA Mutation | p.Arg355His(p.R355H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50179032:50179032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759648297 |
| CDS Mutation | c.1789G>A |
| AA Mutation | p.Ala597Thr(p.A597T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177710:50177710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998G>A |
| AA Mutation | p.Arg333His(p.R333H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177426:50177426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.714C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177558:50177558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.846G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177501:50177501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745726556 |
| CDS Mutation | c.789G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177231:50177231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.519G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177105:50177105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.393C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395842 |
| Start | 50178113:50178113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755399207 |
| CDS Mutation | c.1401G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177282:50177282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.570C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395842 |
| Start | 50177363:50177363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.651C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000395842 |
| Start | 50179187:50179187(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1948delG |
| AA Mutation | p.Asp650ThrfsTer23(p.D650Tfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000395842 |
| Start | 50179161:50179161(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs570684262 |
| CDS Mutation | c.1922delG |
| AA Mutation | p.Gly641AlafsTer32(p.G641Afs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |