Primary Site >> Stomach Cancer
Gene >> PALD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70547346:70547346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781013796 |
| CDS Mutation | c.2162G>A |
| AA Mutation | p.Arg721His(p.R721H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70564383:70564383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766925536 |
| CDS Mutation | c.2282C>T |
| AA Mutation | p.Ala761Val(p.A761V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70537893:70537893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1310A>G |
| AA Mutation | p.Tyr437Cys(p.Y437C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70531336:70531336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140490112 |
| CDS Mutation | c.515G>A |
| AA Mutation | p.Arg172His(p.R172H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70525962:70525962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746010656 |
| CDS Mutation | c.11C>T |
| AA Mutation | p.Thr4Met(p.T4M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70547328:70547328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757741108 |
| CDS Mutation | c.2144T>C |
| AA Mutation | p.Leu715Pro(p.L715P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70538346:70538346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1390C>T |
| AA Mutation | p.Pro464Ser(p.P464S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70539095:70539095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1573C>A |
| AA Mutation | p.Leu525Met(p.L525M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70525991:70525991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.40G>A |
| AA Mutation | p.Ala14Thr(p.A14T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70526019:70526019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.68G>A |
| AA Mutation | p.Gly23Asp(p.G23D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263563 |
| Start | 70541213:70541213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2020G>A |
| AA Mutation | p.Val674Met(p.V674M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263563 |
| Start | 70532626:70532626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769539071 |
| CDS Mutation | c.639C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263563 |
| Start | 70537897:70537897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1314T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263563 |
| Start | 70539639:70539639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760096524 |
| CDS Mutation | c.1785C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263563 |
| Start | 70539749:70539749(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1900delC |
| AA Mutation | p.Arg634GlufsTer61(p.R634Efs*61) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263563 |
| Start | 70533964:70533964(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.917delC |
| AA Mutation | p.Pro306GlnfsTer52(p.P306Qfs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263563 |
| Start | 70539748:70539749(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs745381684 |
| CDS Mutation | c.1900dupC |
| AA Mutation | p.Arg634ProfsTer6(p.R634Pfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |