Primary Site >> Stomach Cancer
Gene >> NGFR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000172229 |
| Start | 49506452:49506452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.362G>A |
| AA Mutation | p.Arg121His(p.R121H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000172229 |
| Start | 49510496:49510496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.653C>A |
| AA Mutation | p.Pro218His(p.P218H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000172229 |
| Start | 49512813:49512813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1088C>T |
| AA Mutation | p.Ala363Val(p.A363V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000172229 |
| Start | 49506406:49506406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.316G>A |
| AA Mutation | p.Val106Met(p.V106M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000172229 |
| Start | 49510567:49510567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.724G>A |
| AA Mutation | p.Val242Met(p.V242M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000172229 |
| Start | 49513002:49513002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574245308 |
| CDS Mutation | c.1277C>T |
| AA Mutation | p.Pro426Leu(p.P426L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000172229 |
| Start | 49506378:49506378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.288G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000172229 |
| Start | 49512778:49512778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1053C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000172229 |
| Start | 49506306:49506306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.216G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000172229 |
| Start | 49506474:49506474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.384C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000172229 |
| Start | 49511988:49511988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.918C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000172229 |
| Start | 49512721:49512721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143961715 |
| CDS Mutation | c.996C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |