Primary Site >> Stomach Cancer
Gene >> GRHL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251808 |
| Start | 101666687:101666687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748576840 |
| CDS Mutation | c.1862C>T |
| AA Mutation | p.Thr621Met(p.T621M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251808 |
| Start | 101644159:101644159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780540983 |
| CDS Mutation | c.1546C>T |
| AA Mutation | p.Arg516Trp(p.R516W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251808 |
| Start | 101558784:101558784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.650G>A |
| AA Mutation | p.Ser217Asn(p.S217N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251808 |
| Start | 101558593:101558593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.459G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251808 |
| Start | 101558713:101558713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144668624 |
| CDS Mutation | c.579C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251808 |
| Start | 101649424:101649424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753392037 |
| CDS Mutation | c.1623C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000251808 |
| Start | 101577438:101577438(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.926delA |
| AA Mutation | p.Asn309ThrfsTer53(p.N309Tfs*53) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |