Primary Site >> Stomach Cancer
Gene >> NOLC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605788 |
| Start | 102157276:102157276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.264G>T |
| AA Mutation | p.Glu88Asp(p.E88D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605788 |
| Start | 102159904:102159904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.868A>G |
| AA Mutation | p.Ser290Gly(p.S290G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605788 |
| Start | 102159554:102159554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.845T>C |
| AA Mutation | p.Met282Thr(p.M282T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605788 |
| Start | 102160586:102160586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767624483 |
| CDS Mutation | c.1234G>A |
| AA Mutation | p.Gly412Ser(p.G412S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605788 |
| Start | 102157064:102157064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166T>G |
| AA Mutation | p.Phe56Val(p.F56V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605788 |
| Start | 102159494:102159494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764883022 |
| CDS Mutation | c.785G>A |
| AA Mutation | p.Arg262Gln(p.R262Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000605788 |
| Start | 102160234:102160234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.990T>G |
| AA Mutation | p.Asp330Glu(p.D330E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605788 |
| Start | 102161633:102161633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1819A>G |
| AA Mutation | p.Thr607Ala(p.T607A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000605788 |
| Start | 102162263:102162263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767225889 |
| CDS Mutation | c.2094C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000605788 |
| Start | 102159260:102159260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.675T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000605788 |
| Start | 102159542:102159542(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs759637346 |
| CDS Mutation | c.840delA |
| AA Mutation | p.Lys280AsnfsTer3(p.K280Nfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000605788 |
| Start | 102159234:102159245(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs746559763 |
| CDS Mutation | c.657_668delTAGCAGCAGCAG |
| AA Mutation | p.Ser224_Ser227del(p.S224_S227del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |