Primary Site >> Stomach Cancer
Gene >> IKZF3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346872 |
| Start | 39765963:39765963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1357C>T |
| AA Mutation | p.Arg453Trp(p.R453W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346872 |
| Start | 39766106:39766106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1214A>G |
| AA Mutation | p.His405Arg(p.H405R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346872 |
| Start | 39791478:39791478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.530A>G |
| AA Mutation | p.His177Arg(p.H177R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346872 |
| Start | 39765947:39765947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761982738 |
| CDS Mutation | c.1373G>A |
| AA Mutation | p.Arg458His(p.R458H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346872 |
| Start | 39766134:39766134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748446589 |
| CDS Mutation | c.1186C>T |
| AA Mutation | p.Arg396Cys(p.R396C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000346872 |
| Start | 39766393:39766393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.927T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000346872 |
| Start | 39792917:39792917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.180G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000346872 |
| Start | 39766324:39766324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760230065 |
| CDS Mutation | c.996G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000346872 |
| Start | 39792863:39792863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.234A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000346872 |
| Start | 39792737:39792737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748258169 |
| CDS Mutation | c.360C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |