Primary Site >> Stomach Cancer
Gene >> ENPP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075322 |
| Start | 119600742:119600742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.908T>C |
| AA Mutation | p.Val303Ala(p.V303A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075322 |
| Start | 119582582:119582582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764975897 |
| CDS Mutation | c.1564G>A |
| AA Mutation | p.Ala522Thr(p.A522T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000075322 |
| Start | 119601460:119601460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.836T>C |
| AA Mutation | p.Val279Ala(p.V279A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075322 |
| Start | 119569284:119569284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2004G>T |
| AA Mutation | p.Leu668Phe(p.L668F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075322 |
| Start | 119607965:119607965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.790G>A |
| AA Mutation | p.Ala264Thr(p.A264T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075322 |
| Start | 119583774:119583774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1486A>G |
| AA Mutation | p.Lys496Glu(p.K496E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075322 |
| Start | 119638448:119638448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.113G>A |
| AA Mutation | p.Gly38Glu(p.G38E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075322 |
| Start | 119564895:119564895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2192T>G |
| AA Mutation | p.Val731Gly(p.V731G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075322 |
| Start | 119586246:119586246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1307C>T |
| AA Mutation | p.Ala436Val(p.A436V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000075322 |
| Start | 119569359:119569359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1929C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000075322 |
| Start | 119600723:119600723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.927G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000075322 |
| Start | 119569341:119569341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1947G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000075322 |
| Start | 119626704:119626704(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.153delC |
| AA Mutation | p.Trp52GlyfsTer44(p.W52Gfs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000075322 |
| Start | 119586305:119586305(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1248delA |
| AA Mutation | p.Lys416AsnfsTer10(p.K416Nfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000075322 |
| Start | 119570821:119570821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764313249 |
| CDS Mutation | c.1801C>T |
| AA Mutation | p.Arg601Ter(p.R601*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |