Primary Site >> Stomach Cancer
Gene >> PLXND1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129565962:129565962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4247T>C |
| AA Mutation | p.Leu1416Pro(p.L1416P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129565500:129565500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4361G>A |
| AA Mutation | p.Gly1454Asp(p.G1454D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000324093 |
| Start | 129571678:129571678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776923438 |
| CDS Mutation | c.3244A>G |
| AA Mutation | p.Ser1082Gly(p.S1082G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129558564:129558564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5309G>A |
| AA Mutation | p.Arg1770Gln(p.R1770Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129585965:129585965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773387450 |
| CDS Mutation | c.1838G>A |
| AA Mutation | p.Arg613His(p.R613H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129583652:129583652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201008545 |
| CDS Mutation | c.2156C>T |
| AA Mutation | p.Ser719Leu(p.S719L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129574389:129574389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141047735 |
| CDS Mutation | c.2632C>T |
| AA Mutation | p.Arg878Trp(p.R878W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129561867:129561867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759954775 |
| CDS Mutation | c.4862G>A |
| AA Mutation | p.Arg1621Gln(p.R1621Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129589365:129589365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754446744 |
| CDS Mutation | c.1474G>A |
| AA Mutation | p.Gly492Arg(p.G492R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129560421:129560421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5042A>G |
| AA Mutation | p.Asp1681Gly(p.D1681G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129606327:129606327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.313C>T |
| AA Mutation | p.His105Tyr(p.H105Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129605919:129605919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.721C>T |
| AA Mutation | p.Arg241Cys(p.R241C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129562895:129562895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753978969 |
| CDS Mutation | c.4717C>T |
| AA Mutation | p.Arg1573Trp(p.R1573W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129567508:129567508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752691422 |
| CDS Mutation | c.4070G>A |
| AA Mutation | p.Arg1357His(p.R1357H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129571119:129571119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3521C>A |
| AA Mutation | p.Pro1174His(p.P1174H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129589389:129589389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1450G>T |
| AA Mutation | p.Ala484Ser(p.A484S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129556624:129556624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369952557 |
| CDS Mutation | c.5654G>A |
| AA Mutation | p.Arg1885Gln(p.R1885Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324093 |
| Start | 129571101:129571101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528635984 |
| CDS Mutation | c.3539C>T |
| AA Mutation | p.Thr1180Met(p.T1180M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324093 |
| Start | 129565439:129565439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138273738 |
| CDS Mutation | c.4422G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324093 |
| Start | 129605944:129605944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.696C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324093 |
| Start | 129561857:129561857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529197578 |
| CDS Mutation | c.4872C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324093 |
| Start | 129605818:129605818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.822G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324093 |
| Start | 129573725:129573725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771219903 |
| CDS Mutation | c.2706G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324093 |
| Start | 129559655:129559655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768576905 |
| CDS Mutation | c.5262C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324093 |
| Start | 129563235:129563235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779508344 |
| CDS Mutation | c.4527G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324093 |
| Start | 129567779:129567779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3892C>T |
| AA Mutation | p.Arg1298Ter(p.R1298*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000324093 |
| Start | 129571039:129571039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751249482 |
| CDS Mutation | c.3600+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |