Primary Site >> Stomach Cancer
Gene >> DOCK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127052794:127052794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2252G>A |
| AA Mutation | p.Arg751His(p.R751H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127447468:127447468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748393302 |
| CDS Mutation | c.5425G>A |
| AA Mutation | p.Ala1809Thr(p.A1809T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127052752:127052752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2210A>C |
| AA Mutation | p.Lys737Thr(p.K737T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127037796:127037796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745478937 |
| CDS Mutation | c.1927G>A |
| AA Mutation | p.Asp643Asn(p.D643N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 126999390:126999390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.804A>T |
| AA Mutation | p.Leu268Phe(p.L268F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127110319:127110319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2525T>C |
| AA Mutation | p.Ile842Thr(p.I842T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127106256:127106256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373968953 |
| CDS Mutation | c.2408C>T |
| AA Mutation | p.Thr803Met(p.T803M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127409148:127409148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4171G>T |
| AA Mutation | p.Gly1391Cys(p.G1391C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 126996801:126996801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.527C>A |
| AA Mutation | p.Pro176Gln(p.P176Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127381294:127381294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3670T>C |
| AA Mutation | p.Cys1224Arg(p.C1224R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127362141:127362141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769248529 |
| CDS Mutation | c.3298C>T |
| AA Mutation | p.Arg1100Cys(p.R1100C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127426000:127426000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779105233 |
| CDS Mutation | c.4840G>A |
| AA Mutation | p.Val1614Ile(p.V1614I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127374186:127374186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3584A>C |
| AA Mutation | p.Asn1195Thr(p.N1195T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280333 |
| Start | 127031739:127031739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1651C>T |
| AA Mutation | p.Leu551Phe(p.L551F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280333 |
| Start | 126998229:126998229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372684802 |
| CDS Mutation | c.747T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280333 |
| Start | 127127740:127127740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2760C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280333 |
| Start | 127384859:127384859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3814C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280333 |
| Start | 126977967:126977967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777561205 |
| CDS Mutation | c.150G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280333 |
| Start | 127043144:127043144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374112333 |
| CDS Mutation | c.2118T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280333 |
| Start | 127409114:127409114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4137A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280333 |
| Start | 127043072:127043072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2046C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280333 |
| Start | 127052765:127052765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761104711 |
| CDS Mutation | c.2223G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000280333 |
| Start | 127439128:127439128(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5104delA |
| AA Mutation | p.Arg1702GlyfsTer26(p.R1702Gfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000280333 |
| Start | 127447441:127447441(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5402delC |
| AA Mutation | p.Pro1801LeufsTer14(p.P1801Lfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000280333 |
| Start | 127404324:127404325(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3960dupA |
| AA Mutation | p.Gln1321ThrfsTer6(p.Q1321Tfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000280333 |
| Start | 127000192:127000193(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.874dupA |
| AA Mutation | p.Arg292LysfsTer51(p.R292Kfs*51) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000280333 |
| Start | 127374122:127374124(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3522_3524delTGT |
| AA Mutation | p.Val1175del(p.V1175del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |