Primary Site >> Stomach Cancer
Gene >> DOC2A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350119 |
| Start | 30007206:30007206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.621G>T |
| AA Mutation | p.Lys207Asn(p.K207N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350119 |
| Start | 30006934:30006934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.729G>T |
| AA Mutation | p.Glu243Asp(p.E243D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350119 |
| Start | 30007231:30007231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.596G>A |
| AA Mutation | p.Arg199His(p.R199H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350119 |
| Start | 30006938:30006938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772945741 |
| CDS Mutation | c.725C>T |
| AA Mutation | p.Ala242Val(p.A242V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350119 |
| Start | 30006897:30006897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.766C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000350119 |
| Start | 30010032:30010032(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs753153258 |
| CDS Mutation | c.191delC |
| AA Mutation | p.Pro64LeufsTer27(p.P64Lfs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |