Primary Site >> Stomach Cancer
Gene >> GRHL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324907 |
| Start | 9995898:9995898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1519C>A |
| AA Mutation | p.Pro507Thr(p.P507T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324907 |
| Start | 9962482:9962482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748306312 |
| CDS Mutation | c.697C>T |
| AA Mutation | p.Arg233Trp(p.R233W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324907 |
| Start | 9990706:9990706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548450490 |
| CDS Mutation | c.1280G>A |
| AA Mutation | p.Arg427Gln(p.R427Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324907 |
| Start | 10000697:10000697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143356570 |
| CDS Mutation | c.1847C>T |
| AA Mutation | p.Thr616Met(p.T616M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324907 |
| Start | 9963927:9963927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.788G>A |
| AA Mutation | p.Arg263Gln(p.R263Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324907 |
| Start | 9961428:9961428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140278187 |
| CDS Mutation | c.661G>A |
| AA Mutation | p.Val221Ile(p.V221I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324907 |
| Start | 9965324:9965324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367582209 |
| CDS Mutation | c.1053C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324907 |
| Start | 9954921:9954921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.27G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324907 |
| Start | 10000671:10000672(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs752756443 |
| CDS Mutation | c.1827dupG |
| AA Mutation | p.Ser610ValfsTer68(p.S610Vfs*68) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |