Primary Site >> Stomach Cancer
Gene >> BDNF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356660 |
| Start | 27658185:27658185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.380G>A |
| AA Mutation | p.Arg127Gln(p.R127Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356660 |
| Start | 27658453:27658453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771341699 |
| CDS Mutation | c.112C>T |
| AA Mutation | p.Arg38Trp(p.R38W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356660 |
| Start | 27658147:27658147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774985498 |
| CDS Mutation | c.418G>A |
| AA Mutation | p.Val140Met(p.V140M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356660 |
| Start | 27657945:27657945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.620A>C |
| AA Mutation | p.Gln207Pro(p.Q207P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356660 |
| Start | 27658478:27658478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.87A>C |
| AA Mutation | p.Gln29His(p.Q29H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356660 |
| Start | 27658245:27658245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.320T>C |
| AA Mutation | p.Leu107Pro(p.L107P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356660 |
| Start | 27658330:27658330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.235C>T |
| AA Mutation | p.Pro79Ser(p.P79S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356660 |
| Start | 27658011:27658011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.554A>G |
| AA Mutation | p.Lys185Arg(p.K185R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356660 |
| Start | 27657995:27657995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.570T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356660 |
| Start | 27658076:27658076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764711746 |
| CDS Mutation | c.489G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |