Primary Site >> Stomach Cancer
Gene >> DDB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61304032:61304032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2665C>T |
| AA Mutation | p.Arg889Trp(p.R889W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61302278:61302278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3194T>C |
| AA Mutation | p.Val1065Ala(p.V1065A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61311815:61311815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2246C>T |
| AA Mutation | p.Thr749Met(p.T749M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61324067:61324067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.833G>A |
| AA Mutation | p.Gly278Asp(p.G278D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61329367:61329367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.545A>G |
| AA Mutation | p.Tyr182Cys(p.Y182C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61323036:61323036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.980G>A |
| AA Mutation | p.Arg327His(p.R327H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61331568:61331568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.185C>T |
| AA Mutation | p.Ala62Val(p.A62V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61312041:61312041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2113G>A |
| AA Mutation | p.Asp705Asn(p.D705N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61303076:61303076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2912C>T |
| AA Mutation | p.Ala971Val(p.A971V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61303915:61303915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2782C>T |
| AA Mutation | p.Arg928Cys(p.R928C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301764 |
| Start | 61329574:61329574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.338G>A |
| AA Mutation | p.Gly113Asp(p.G113D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301764 |
| Start | 61312078:61312078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753624809 |
| CDS Mutation | c.2076G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301764 |
| Start | 61326876:61326876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553636034 |
| CDS Mutation | c.567C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301764 |
| Start | 61303075:61303075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779141182 |
| CDS Mutation | c.2913C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301764 |
| Start | 61314421:61314421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1476G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301764 |
| Start | 61303925:61303925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2772C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301764 |
| Start | 61326807:61326807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754810752 |
| CDS Mutation | c.636C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000301764 |
| Start | 61302625:61302625(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3069delC |
| AA Mutation | p.Thr1024HisfsTer13(p.T1024Hfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000301764 |
| Start | 61314315:61314315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1582C>T |
| AA Mutation | p.Gln528Ter(p.Q528*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000301764 |
| Start | 61326851:61326851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780534106 |
| CDS Mutation | c.592C>T |
| AA Mutation | p.Arg198Ter(p.R198*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |