Primary Site >> Stomach Cancer
Gene >> NRP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205794814:205794814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761518491 |
| CDS Mutation | c.2552C>T |
| AA Mutation | p.Ser851Leu(p.S851L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205727901:205727901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769522962 |
| CDS Mutation | c.1001G>A |
| AA Mutation | p.Arg334His(p.R334H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205745866:205745866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1762G>A |
| AA Mutation | p.Glu588Lys(p.E588K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205743308:205743308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1397G>A |
| AA Mutation | p.Arg466His(p.R466H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205752972:205752972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2041C>T |
| AA Mutation | p.Pro681Ser(p.P681S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205743233:205743233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1322T>C |
| AA Mutation | p.Leu441Pro(p.L441P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205727997:205727997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1097G>A |
| AA Mutation | p.Ser366Asn(p.S366N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205722508:205722508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.464G>A |
| AA Mutation | p.Ser155Asn(p.S155N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205763878:205763878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2249A>G |
| AA Mutation | p.Gln750Arg(p.Q750R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205740600:205740600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1228C>T |
| AA Mutation | p.Arg410Cys(p.R410C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205743475:205743475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1564C>T |
| AA Mutation | p.Arg522Cys(p.R522C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360409 |
| Start | 205716271:205716271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751590695 |
| CDS Mutation | c.330G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360409 |
| Start | 205743378:205743378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1467G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360409 |
| Start | 205765509:205765509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758235220 |
| CDS Mutation | c.2343C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360409 |
| Start | 205763807:205763808(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2182dupG |
| AA Mutation | p.Val728GlyfsTer21(p.V728Gfs*21) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |