Primary Site >> Stomach Cancer
Gene >> RTN4R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000043402 |
| Start | 20242093:20242093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1040T>C |
| AA Mutation | p.Leu347Pro(p.L347P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000043402 |
| Start | 20242424:20242424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.709A>G |
| AA Mutation | p.Asn237Asp(p.N237D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000043402 |
| Start | 20242516:20242516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.617G>A |
| AA Mutation | p.Arg206His(p.R206H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000043402 |
| Start | 20242898:20242898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.235G>A |
| AA Mutation | p.Ala79Thr(p.A79T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000043402 |
| Start | 20242778:20242778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs74315508 |
| CDS Mutation | c.355C>T |
| AA Mutation | p.Arg119Trp(p.R119W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000043402 |
| Start | 20242608:20242608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140080129 |
| CDS Mutation | c.525C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000043402 |
| Start | 20243049:20243049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.84A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000043402 |
| Start | 20242989:20242989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.144G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000043402 |
| Start | 20243087:20243087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.46C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000043402 |
| Start | 20242641:20242641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368044171 |
| CDS Mutation | c.492C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |