Primary Site >> Stomach Cancer
Gene >> ZNF143
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396602 |
| Start | 9471376:9471376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762077968 |
| CDS Mutation | c.68C>T |
| AA Mutation | p.Ala23Val(p.A23V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396602 |
| Start | 9512484:9512484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1412C>T |
| AA Mutation | p.Thr471Met(p.T471M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396602 |
| Start | 9508762:9508762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1291A>G |
| AA Mutation | p.Thr431Ala(p.T431A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396602 |
| Start | 9512577:9512577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1505C>A |
| AA Mutation | p.Ser502Tyr(p.S502Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396602 |
| Start | 9525277:9525277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1724C>G |
| AA Mutation | p.Thr575Ser(p.T575S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396602 |
| Start | 9478472:9478472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768970571 |
| CDS Mutation | c.456G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396602 |
| Start | 9501116:9501116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147334022 |
| CDS Mutation | c.993C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396602 |
| Start | 9478418:9478418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201240423 |
| CDS Mutation | c.402G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |