Primary Site >> Stomach Cancer
Gene >> LIPF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238983 |
| Start | 88667673:88667673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.210T>A |
| AA Mutation | p.Asn70Lys(p.N70K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238983 |
| Start | 88667362:88667362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.65G>A |
| AA Mutation | p.Gly22Glu(p.G22E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238983 |
| Start | 88669914:88669914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.500A>G |
| AA Mutation | p.His167Arg(p.H167R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238983 |
| Start | 88668738:88668738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.404T>A |
| AA Mutation | p.Val135Asp(p.V135D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238983 |
| Start | 88678604:88678604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150812830 |
| CDS Mutation | c.1120G>C |
| AA Mutation | p.Asp374His(p.D374H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238983 |
| Start | 88678647:88678647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1163A>G |
| AA Mutation | p.Asp388Gly(p.D388G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000238983 |
| Start | 88668755:88668755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.421A>C |
| AA Mutation | p.Ser141Arg(p.S141R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238983 |
| Start | 88675627:88675627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.858T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238983 |
| Start | 88668628:88668628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140420172 |
| CDS Mutation | c.294G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000238983 |
| Start | 88678569:88678569(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1087delT |
| AA Mutation | p.Tyr363ThrfsTer30(p.Y363Tfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000238983 |
| Start | 88676280:88676281(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.960_960+1insTCCCAACCTCCCTACTACAATGTGACAGCCAT |
| AA Mutation | p.Met331IlefsTer9(p.M331Ifs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000238983 |
| Start | 88667572:88667573(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.110dupA |
| AA Mutation | p.Met38AspfsTer10(p.M38Dfs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000238983 |
| Start | 88667316:88667317(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.20_29dupTGGCAAGTTT |
| AA Mutation | p.Leu10PhefsTer24(p.L10Ffs*24) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |