Primary Site >> Stomach Cancer
Gene >> PAX2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428433 |
| Start | 100827581:100827581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1216G>A |
| AA Mutation | p.Ala406Thr(p.A406T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428433 |
| Start | 100749808:100749808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770252038 |
| CDS Mutation | c.106G>A |
| AA Mutation | p.Val36Met(p.V36M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428433 |
| Start | 100806478:100806478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.734A>G |
| AA Mutation | p.Asp245Gly(p.D245G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428433 |
| Start | 100827023:100827023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1105G>A |
| AA Mutation | p.Gly369Ser(p.G369S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428433 |
| Start | 100749777:100749777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371041678 |
| CDS Mutation | c.75G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000428433 |
| Start | 100827567:100827567(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1207delC |
| AA Mutation | p.Arg403GlyfsTer37(p.R403Gfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000428433 |
| Start | 100749771:100749772(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs768607170 |
| CDS Mutation | c.76dupG |
| AA Mutation | p.Val26GlyfsTer28(p.V26Gfs*28) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |