Primary Site >> Stomach Cancer
Gene >> PPL
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000345988 |
| Start | 4893213:4893213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1650G>T |
| AA Mutation | p.Lys550Asn(p.K550N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4884704:4884704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3951G>T |
| AA Mutation | p.Glu1317Asp(p.E1317D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4894474:4894474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1387G>T |
| AA Mutation | p.Ala463Ser(p.A463S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4883689:4883689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140094738 |
| CDS Mutation | c.4966C>T |
| AA Mutation | p.Arg1656Cys(p.R1656C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4884288:4884288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146493629 |
| CDS Mutation | c.4367C>T |
| AA Mutation | p.Ala1456Val(p.A1456V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4893362:4893362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1501G>A |
| AA Mutation | p.Asp501Asn(p.D501N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4892191:4892191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753868819 |
| CDS Mutation | c.1673G>A |
| AA Mutation | p.Arg558Gln(p.R558Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4899044:4899044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200614178 |
| CDS Mutation | c.845C>T |
| AA Mutation | p.Ala282Val(p.A282V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4884483:4884483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573477337 |
| CDS Mutation | c.4172G>A |
| AA Mutation | p.Arg1391Gln(p.R1391Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4901036:4901036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.492A>C |
| AA Mutation | p.Gln164His(p.Q164H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000345988 |
| Start | 4894617:4894617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1244G>A |
| AA Mutation | p.Gly415Asp(p.G415D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4885615:4885615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767821204 |
| CDS Mutation | c.3040C>T |
| AA Mutation | p.Arg1014Trp(p.R1014W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4885408:4885408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3247C>T |
| AA Mutation | p.Leu1083Phe(p.L1083F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4900861:4900861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767203015 |
| CDS Mutation | c.575G>T |
| AA Mutation | p.Ser192Ile(p.S192I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4892153:4892153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138181414 |
| CDS Mutation | c.1711G>A |
| AA Mutation | p.Glu571Lys(p.E571K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4897715:4897715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.932G>A |
| AA Mutation | p.Cys311Tyr(p.C311Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4883733:4883733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4922G>C |
| AA Mutation | p.Gly1641Ala(p.G1641A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345988 |
| Start | 4901072:4901072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.456G>T |
| AA Mutation | p.Gln152His(p.Q152H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345988 |
| Start | 4883849:4883849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778246100 |
| CDS Mutation | c.4806G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345988 |
| Start | 4894523:4894523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141007351 |
| CDS Mutation | c.1338G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345988 |
| Start | 4884125:4884125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4530C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345988 |
| Start | 4885220:4885220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3435C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345988 |
| Start | 4885103:4885103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370446525 |
| CDS Mutation | c.3552G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345988 |
| Start | 4885286:4885286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761315817 |
| CDS Mutation | c.3369C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345988 |
| Start | 4884377:4884377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4278G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345988 |
| Start | 4890784:4890784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2106C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345988 |
| Start | 4883783:4883783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4872G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000345988 |
| Start | 4885688:4885688(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2967delG |
| AA Mutation | p.Gln990ArgfsTer31(p.Q990Rfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000345988 |
| Start | 4902484:4902484(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.360delA |
| AA Mutation | p.Lys120AsnfsTer10(p.K120Nfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000345988 |
| Start | 4894499:4894499(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs779128891 |
| CDS Mutation | c.1362delC |
| AA Mutation | p.Thr455GlnfsTer37(p.T455Qfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000345988 |
| Start | 4885066:4885089(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3566_3589delCGAACCTCCGCCTGGAGCTTGTGG |
| AA Mutation | p.Ala1189_Val1196del(p.A1189_V1196del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |