Primary Site >> Stomach Cancer
Gene >> GRHL3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350501 |
| Start | 24342901:24342901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1295G>A |
| AA Mutation | p.Gly432Asp(p.G432D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350501 |
| Start | 24337740:24337740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184435420 |
| CDS Mutation | c.791G>A |
| AA Mutation | p.Arg264Gln(p.R264Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350501 |
| Start | 24346566:24346566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375906769 |
| CDS Mutation | c.1468C>T |
| AA Mutation | p.Arg490Cys(p.R490C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350501 |
| Start | 24343014:24343014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1408C>T |
| AA Mutation | p.Arg470Cys(p.R470C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350501 |
| Start | 24339699:24339699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.984G>T |
| AA Mutation | p.Glu328Asp(p.E328D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350501 |
| Start | 24342711:24342711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1224G>A |
| AA Mutation | p.Met408Ile(p.M408I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350501 |
| Start | 24342712:24342712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1225C>A |
| AA Mutation | p.Arg409Ser(p.R409S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350501 |
| Start | 24337995:24337995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.844G>A |
| AA Mutation | p.Val282Met(p.V282M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350501 |
| Start | 24336786:24336786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200674358 |
| CDS Mutation | c.571C>T |
| AA Mutation | p.Arg191Cys(p.R191C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350501 |
| Start | 24336572:24336572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.357A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350501 |
| Start | 24342968:24342968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370513043 |
| CDS Mutation | c.1362G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350501 |
| Start | 24342914:24342914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370928369 |
| CDS Mutation | c.1308G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000350501 |
| Start | 24337658:24337659(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.714dupC |
| AA Mutation | p.Lys239GlnfsTer52(p.K239Qfs*52) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |