Primary Site >> Stomach Cancer
Gene >> PAX8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263334 |
| Start | 113244461:113244461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.355A>G |
| AA Mutation | p.Asn119Asp(p.N119D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263334 |
| Start | 113242770:113242770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.398G>A |
| AA Mutation | p.Arg133Gln(p.R133Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263334 |
| Start | 113244602:113244602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.214C>T |
| AA Mutation | p.Arg72Trp(p.R72W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263334 |
| Start | 113246842:113246842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.103G>A |
| AA Mutation | p.Val35Ile(p.V35I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263334 |
| Start | 113246800:113246800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755170424 |
| CDS Mutation | c.145C>T |
| AA Mutation | p.Arg49Cys(p.R49C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263334 |
| Start | 113244471:113244471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772686587 |
| CDS Mutation | c.345C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263334 |
| Start | 113235545:113235545(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.936delC |
| AA Mutation | p.Glu313ArgfsTer113(p.E313Rfs*113) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |