Primary Site >> Stomach Cancer
Gene >> PLXNA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208043154:208043154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3924C>G |
| AA Mutation | p.Asp1308Glu(p.D1308E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208031746:208031746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5069A>C |
| AA Mutation | p.Lys1690Thr(p.K1690T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208142451:208142451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147087031 |
| CDS Mutation | c.1384G>A |
| AA Mutation | p.Gly462Ser(p.G462S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208046056:208046056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3317A>G |
| AA Mutation | p.Tyr1106Cys(p.Y1106C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367033 |
| Start | 208042098:208042098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4286G>A |
| AA Mutation | p.Arg1429Lys(p.R1429K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208052337:208052337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766742913 |
| CDS Mutation | c.2983G>A |
| AA Mutation | p.Glu995Lys(p.E995K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208028974:208028974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5294G>T |
| AA Mutation | p.Ser1765Ile(p.S1765I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208044532:208044532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3850C>T |
| AA Mutation | p.Arg1284Cys(p.R1284C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208084517:208084517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2161A>G |
| AA Mutation | p.Thr721Ala(p.T721A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208217015:208217015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.908C>G |
| AA Mutation | p.Ala303Gly(p.A303G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208044708:208044708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140111660 |
| CDS Mutation | c.3674C>T |
| AA Mutation | p.Ser1225Leu(p.S1225L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208052343:208052343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2977A>G |
| AA Mutation | p.Thr993Ala(p.T993A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208217225:208217225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.698T>C |
| AA Mutation | p.Leu233Pro(p.L233P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208033404:208033404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4970A>G |
| AA Mutation | p.Asn1657Ser(p.N1657S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208084394:208084394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2284T>C |
| AA Mutation | p.Cys762Arg(p.C762R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208079424:208079424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373107594 |
| CDS Mutation | c.2422C>T |
| AA Mutation | p.Arg808Trp(p.R808W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208038881:208038881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566013352 |
| CDS Mutation | c.4604C>T |
| AA Mutation | p.Ala1535Val(p.A1535V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367033 |
| Start | 208034493:208034493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780055079 |
| CDS Mutation | c.4864G>A |
| AA Mutation | p.Asp1622Asn(p.D1622N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367033 |
| Start | 208096067:208096067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747915596 |
| CDS Mutation | c.1944C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367033 |
| Start | 208217539:208217539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.384C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367033 |
| Start | 208029018:208029018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760490787 |
| CDS Mutation | c.5250C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367033 |
| Start | 208092870:208092870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2013C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367033 |
| Start | 208217338:208217338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.585C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367033 |
| Start | 208217365:208217365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.558G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367033 |
| Start | 208028135:208028135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5463C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367033 |
| Start | 208044647:208044647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201569933 |
| CDS Mutation | c.3735C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367033 |
| Start | 208217742:208217742(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.181delG |
| AA Mutation | p.Ala61ProfsTer13(p.A61Pfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367033 |
| Start | 208043111:208043111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758315833 |
| CDS Mutation | c.3967C>T |
| AA Mutation | p.Arg1323Ter(p.R1323*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367033 |
| Start | 208054474:208054475(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2802dupT |
| AA Mutation | p.Gly935TrpfsTer4(p.G935Wfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000367033 |
| Start | 208210387:208210419(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1232_1264delAGCCCCTGGGAGGCTCAACTCCAGTGGAGGGCC |
| AA Mutation | p.Gln411_Gly421del(p.Q411_G421del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |