Primary Site >> Stomach Cancer
Gene >> PLD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4818328:4818328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1952G>T |
| AA Mutation | p.Arg651Leu(p.R651L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4818809:4818809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2159G>A |
| AA Mutation | p.Arg720His(p.R720H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4817236:4817236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368012043 |
| CDS Mutation | c.1792G>A |
| AA Mutation | p.Gly598Arg(p.G598R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4822706:4822706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2644G>A |
| AA Mutation | p.Glu882Lys(p.E882K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4819494:4819494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369879187 |
| CDS Mutation | c.2374G>A |
| AA Mutation | p.Glu792Lys(p.E792K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4808392:4808392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769141526 |
| CDS Mutation | c.359T>C |
| AA Mutation | p.Leu120Ser(p.L120S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4818528:4818528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2044C>T |
| AA Mutation | p.Pro682Ser(p.P682S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4816993:4816993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138719274 |
| CDS Mutation | c.1639G>A |
| AA Mutation | p.Val547Ile(p.V547I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4808086:4808086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.212G>A |
| AA Mutation | p.Gly71Asp(p.G71D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4809105:4809105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373362915 |
| CDS Mutation | c.389C>T |
| AA Mutation | p.Ala130Val(p.A130V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4809710:4809710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375978258 |
| CDS Mutation | c.634C>T |
| AA Mutation | p.Arg212Cys(p.R212C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4816980:4816980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1626C>A |
| AA Mutation | p.Asp542Glu(p.D542E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4809771:4809771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.695G>A |
| AA Mutation | p.Arg232His(p.R232H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263088 |
| Start | 4815558:4815558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199737765 |
| CDS Mutation | c.1256C>T |
| AA Mutation | p.Ala419Val(p.A419V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263088 |
| Start | 4816742:4816742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200019208 |
| CDS Mutation | c.1578C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263088 |
| Start | 4822727:4822727(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2670delC |
| AA Mutation | p.Leu891TrpfsTer21(p.L891Wfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263088 |
| Start | 4815844:4815844(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs753325116 |
| CDS Mutation | c.1370delG |
| AA Mutation | p.Gly457AspfsTer16(p.G457Dfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |