Primary Site >> Stomach Cancer
Gene >> APLNR
| ID | 1 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236161:57236161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.844G>A |
| AA Mutation | p.Asp282Asn(p.D282N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236344:57236344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.661T>C |
| AA Mutation | p.Tyr221His(p.Y221H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236874:57236874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767906014 |
| CDS Mutation | c.131C>T |
| AA Mutation | p.Thr44Met(p.T44M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236056:57236056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777561476 |
| CDS Mutation | c.949C>T |
| AA Mutation | p.Arg317Cys(p.R317C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236687:57236687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.318C>A |
| AA Mutation | p.Ser106Arg(p.S106R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236766:57236766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.239T>C |
| AA Mutation | p.Val80Ala(p.V80A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236767:57236767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.238G>T |
| AA Mutation | p.Val80Leu(p.V80L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236569:57236569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755793037 |
| CDS Mutation | c.436G>A |
| AA Mutation | p.Gly146Arg(p.G146R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236502:57236502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746176980 |
| CDS Mutation | c.503G>A |
| AA Mutation | p.Arg168His(p.R168H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57235901:57235901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1104A>T |
| AA Mutation | p.Lys368Asn(p.K368N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57235895:57235895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1110C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236738:57236738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755487685 |
| CDS Mutation | c.267G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236867:57236867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138964036 |
| CDS Mutation | c.138C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant;NMD_transcript_variant |
| Transcription ID | ENST00000257254 |
| Start | 57236849:57236849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747009504 |
| CDS Mutation | c.156C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |