Primary Site >> Stomach Cancer
Gene >> WDR66
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121960680:121960680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2229C>G |
| AA Mutation | p.Ser743Arg(p.S743R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121958391:121958391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1850A>G |
| AA Mutation | p.Tyr617Cys(p.Y617C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121921401:121921401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.96A>C |
| AA Mutation | p.Glu32Asp(p.E32D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121957236:121957236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1698C>G |
| AA Mutation | p.Asp566Glu(p.D566E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121959045:121959045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2084G>A |
| AA Mutation | p.Ser695Asn(p.S695N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121921480:121921480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201510168 |
| CDS Mutation | c.175G>A |
| AA Mutation | p.Glu59Lys(p.E59K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121942583:121942583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747183230 |
| CDS Mutation | c.1048A>G |
| AA Mutation | p.Met350Val(p.M350V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121923716:121923716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.473T>G |
| AA Mutation | p.Phe158Cys(p.F158C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121921590:121921590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.285A>C |
| AA Mutation | p.Glu95Asp(p.E95D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121959086:121959086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2125G>A |
| AA Mutation | p.Ala709Thr(p.A709T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288912 |
| Start | 121968142:121968142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754845886 |
| CDS Mutation | c.2744C>T |
| AA Mutation | p.Ser915Leu(p.S915L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288912 |
| Start | 122001558:122001558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs576412535 |
| CDS Mutation | c.3297C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288912 |
| Start | 121968125:121968125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2727G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288912 |
| Start | 121921620:121921620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370712951 |
| CDS Mutation | c.315G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288912 |
| Start | 121923858:121923858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288912 |
| Start | 121966961:121966961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559061329 |
| CDS Mutation | c.2499G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288912 |
| Start | 122003746:122003746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746253460 |
| CDS Mutation | c.3432C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288912 |
| Start | 121934276:121934276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767249441 |
| CDS Mutation | c.918C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000288912 |
| Start | 121948995:121948995(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1206delT |
| AA Mutation | p.Phe402LeufsTer10(p.F402Lfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |