Primary Site >> Stomach Cancer
Gene >> PLVAP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252590 |
| Start | 17365503:17365503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376519104 |
| CDS Mutation | c.962C>T |
| AA Mutation | p.Ala321Val(p.A321V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252590 |
| Start | 17365594:17365594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141514915 |
| CDS Mutation | c.871C>T |
| AA Mutation | p.Arg291Trp(p.R291W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252590 |
| Start | 17377213:17377213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761581948 |
| CDS Mutation | c.76C>T |
| AA Mutation | p.Arg26Cys(p.R26C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252590 |
| Start | 17376934:17376934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.355T>C |
| AA Mutation | p.Cys119Arg(p.C119R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000252590 |
| Start | 17366195:17366195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.370G>A |
| AA Mutation | p.Val124Ile(p.V124I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252590 |
| Start | 17365502:17365502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150210307 |
| CDS Mutation | c.963G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252590 |
| Start | 17376968:17376968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181770634 |
| CDS Mutation | c.321C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252590 |
| Start | 17365910:17365910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199547779 |
| CDS Mutation | c.555C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252590 |
| Start | 17365667:17365667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.798C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252590 |
| Start | 17365568:17365568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147035073 |
| CDS Mutation | c.897C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |