Primary Site >> Stomach Cancer
Gene >> NPR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153684970:153684970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1491G>A |
| AA Mutation | p.Met497Ile(p.M497I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153687690:153687690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2149T>C |
| AA Mutation | p.Ser717Pro(p.S717P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153690315:153690315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2964G>T |
| AA Mutation | p.Lys988Asn(p.K988N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153681267:153681267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1009T>C |
| AA Mutation | p.Phe337Leu(p.F337L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153689225:153689225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2602C>A |
| AA Mutation | p.Gln868Lys(p.Q868K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153687236:153687236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1972C>T |
| AA Mutation | p.His658Tyr(p.H658Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153689087:153689087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2552A>G |
| AA Mutation | p.Gln851Arg(p.Q851R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153679690:153679690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780404659 |
| CDS Mutation | c.582G>C |
| AA Mutation | p.Glu194Asp(p.E194D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153688196:153688196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753081607 |
| CDS Mutation | c.2392C>T |
| AA Mutation | p.Arg798Cys(p.R798C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153681289:153681289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1031G>A |
| AA Mutation | p.Gly344Asp(p.G344D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368680 |
| Start | 153686160:153686160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145787747 |
| CDS Mutation | c.1718G>A |
| AA Mutation | p.Arg573His(p.R573H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368680 |
| Start | 153685868:153685868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1668A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368680 |
| Start | 153687277:153687277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2013C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368680 |
| Start | 153689284:153689284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141781853 |
| CDS Mutation | c.2661G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |