Primary Site >> Stomach Cancer
Gene >> LDOC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370526 |
| Start | 141176930:141176930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.92G>A |
| AA Mutation | p.Arg31Gln(p.R31Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370526 |
| Start | 141176888:141176888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.134G>A |
| AA Mutation | p.Arg45His(p.R45H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370526 |
| Start | 141176844:141176844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.178G>A |
| AA Mutation | p.Glu60Lys(p.E60K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370526 |
| Start | 141176622:141176622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.400G>A |
| AA Mutation | p.Asp134Asn(p.D134N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370526 |
| Start | 141176825:141176825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.197A>T |
| AA Mutation | p.Glu66Val(p.E66V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370526 |
| Start | 141176835:141176835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782286173 |
| CDS Mutation | c.187C>T |
| AA Mutation | p.Arg63Trp(p.R63W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370526 |
| Start | 141176968:141176968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.54C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |