Primary Site >> Stomach Cancer
Gene >> PLD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171734897:171734897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.508A>T |
| AA Mutation | p.Met170Leu(p.M170L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171662164:171662164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745485055 |
| CDS Mutation | c.2236C>T |
| AA Mutation | p.Arg746Cys(p.R746C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171709605:171709605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527440335 |
| CDS Mutation | c.1016G>A |
| AA Mutation | p.Arg339Gln(p.R339Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171735522:171735522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.404C>T |
| AA Mutation | p.Ala135Val(p.A135V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171738042:171738042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10A>G |
| AA Mutation | p.Lys4Glu(p.K4E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171687553:171687553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1571G>T |
| AA Mutation | p.Arg524Ile(p.R524I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171688713:171688713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1502A>C |
| AA Mutation | p.Lys501Thr(p.K501T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171612357:171612357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2804A>C |
| AA Mutation | p.Glu935Ala(p.E935A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171603182:171603182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3121C>T |
| AA Mutation | p.Arg1041Cys(p.R1041C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171620409:171620409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2705C>T |
| AA Mutation | p.Ala902Val(p.A902V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171674589:171674589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754079957 |
| CDS Mutation | c.2140C>A |
| AA Mutation | p.Leu714Ile(p.L714I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171662074:171662074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2326T>C |
| AA Mutation | p.Tyr776His(p.Y776H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171612313:171612313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373695779 |
| CDS Mutation | c.2848C>T |
| AA Mutation | p.Arg950Trp(p.R950W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171687523:171687523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1601A>G |
| AA Mutation | p.Asn534Ser(p.N534S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171738021:171738021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.31A>T |
| AA Mutation | p.Thr11Ser(p.T11S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351298 |
| Start | 171612318:171612318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2843C>T |
| AA Mutation | p.Ala948Val(p.A948V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351298 |
| Start | 171674506:171674506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757293042 |
| CDS Mutation | c.2223C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351298 |
| Start | 171709691:171709691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.930C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351298 |
| Start | 171737598:171737598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144748395 |
| CDS Mutation | c.222G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351298 |
| Start | 171738037:171738037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145738077 |
| CDS Mutation | c.15C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351298 |
| Start | 171733501:171733501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.549G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351298 |
| Start | 171709583:171709583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1038C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351298 |
| Start | 171688694:171688694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201783123 |
| CDS Mutation | c.1521G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000351298 |
| Start | 171733473:171733473(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.577delA |
| AA Mutation | p.Met193CysfsTer16(p.M193Cfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000351298 |
| Start | 171733500:171733500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.550G>T |
| AA Mutation | p.Glu184Ter(p.E184*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000351298 |
| Start | 171738037:171738038(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.14dupA |
| AA Mutation | p.Asn5LysfsTer16(p.N5Kfs*16) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000351298 |
| Start | 171709710:171709710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.912-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |