Primary Site >> Stomach Cancer
Gene >> PLXNB3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153770863:153770863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782236263 |
| CDS Mutation | c.2116C>T |
| AA Mutation | p.Arg706Trp(p.R706W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153778621:153778621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5572T>G |
| AA Mutation | p.Cys1858Gly(p.C1858G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153773265:153773265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782400714 |
| CDS Mutation | c.2942G>A |
| AA Mutation | p.Arg981His(p.R981H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153778446:153778446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367877344 |
| CDS Mutation | c.5525A>C |
| AA Mutation | p.Asn1842Thr(p.N1842T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153778277:153778277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5426A>T |
| AA Mutation | p.Lys1809Ile(p.K1809I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153770977:153770977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2149T>G |
| AA Mutation | p.Ser717Ala(p.S717A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153775056:153775056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4108C>G |
| AA Mutation | p.Leu1370Val(p.L1370V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153776906:153776906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4853T>G |
| AA Mutation | p.Val1618Gly(p.V1618G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153777552:153777552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5125G>A |
| AA Mutation | p.Asp1709Asn(p.D1709N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153774728:153774728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3853C>T |
| AA Mutation | p.Arg1285Trp(p.R1285W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153775047:153775047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782068600 |
| CDS Mutation | c.4099C>T |
| AA Mutation | p.Arg1367Cys(p.R1367C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153777319:153777319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782063016 |
| CDS Mutation | c.5039G>A |
| AA Mutation | p.Arg1680His(p.R1680H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153777598:153777598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5171C>A |
| AA Mutation | p.Ala1724Asp(p.A1724D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153774963:153774963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781808141 |
| CDS Mutation | c.4015C>T |
| AA Mutation | p.Arg1339Cys(p.R1339C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153774270:153774270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370950098 |
| CDS Mutation | c.3604C>T |
| AA Mutation | p.Arg1202Cys(p.R1202C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153773936:153773936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149200734 |
| CDS Mutation | c.3357G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153768971:153768971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1290C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153770799:153770799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782198666 |
| CDS Mutation | c.2052C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153768275:153768275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782813775 |
| CDS Mutation | c.1113C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153774965:153774965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782612614 |
| CDS Mutation | c.4017C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153774008:153774008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3429G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153775028:153775028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781989622 |
| CDS Mutation | c.4080C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153771924:153771924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781994283 |
| CDS Mutation | c.2578C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153775296:153775296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4227G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153771496:153771496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782041448 |
| CDS Mutation | c.2358C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361971 |
| Start | 153777236:153777236(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs782076287 |
| CDS Mutation | c.4963delG |
| AA Mutation | p.Val1655CysfsTer7(p.V1655Cfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |