Primary Site >> Stomach Cancer
Gene >> DOCK6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11215864:11215864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754447735 |
| CDS Mutation | c.3958C>T |
| AA Mutation | p.Arg1320Trp(p.R1320W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11243610:11243610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1205C>T |
| AA Mutation | p.Ala402Val(p.A402V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11202621:11202621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5324C>T |
| AA Mutation | p.Ser1775Leu(p.S1775L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11252915:11252915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.176T>C |
| AA Mutation | p.Val59Ala(p.V59A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11242186:11242186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763666283 |
| CDS Mutation | c.1502C>A |
| AA Mutation | p.Ser501Tyr(p.S501Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11213286:11213286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4381G>A |
| AA Mutation | p.Asp1461Asn(p.D1461N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11200967:11200967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377350157 |
| CDS Mutation | c.5774C>T |
| AA Mutation | p.Pro1925Leu(p.P1925L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11202677:11202677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5268C>G |
| AA Mutation | p.Phe1756Leu(p.F1756L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11202034:11202034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201858507 |
| CDS Mutation | c.5543G>A |
| AA Mutation | p.Arg1848His(p.R1848H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11215396:11215396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192428488 |
| CDS Mutation | c.4097G>A |
| AA Mutation | p.Arg1366His(p.R1366H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11245688:11245688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.898C>A |
| AA Mutation | p.Leu300Met(p.L300M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11214388:11214388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779004684 |
| CDS Mutation | c.4225C>T |
| AA Mutation | p.Arg1409Trp(p.R1409W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11217335:11217335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751675629 |
| CDS Mutation | c.3607G>A |
| AA Mutation | p.Glu1203Lys(p.E1203K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11252807:11252807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575157102 |
| CDS Mutation | c.284C>T |
| AA Mutation | p.Thr95Met(p.T95M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11251022:11251022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.572T>C |
| AA Mutation | p.Ile191Thr(p.I191T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294618 |
| Start | 11202092:11202092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5485T>C |
| AA Mutation | p.Phe1829Leu(p.F1829L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294618 |
| Start | 11221945:11221945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761619087 |
| CDS Mutation | c.3456C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294618 |
| Start | 11250964:11250964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114634227 |
| CDS Mutation | c.630G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294618 |
| Start | 11245680:11245680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79202547 |
| CDS Mutation | c.906G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294618 |
| Start | 11208773:11208773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201362444 |
| CDS Mutation | c.5001C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294618 |
| Start | 11214628:11214628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372033657 |
| CDS Mutation | c.4128C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294618 |
| Start | 11222897:11222897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375798888 |
| CDS Mutation | c.3078G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294618 |
| Start | 11242074:11242074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750652023 |
| CDS Mutation | c.1614C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000294618 |
| Start | 11245665:11245665(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.921delG |
| AA Mutation | p.Leu308CysfsTer22(p.L308Cfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000294618 |
| Start | 11213265:11213265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752179590 |
| CDS Mutation | c.4402C>T |
| AA Mutation | p.Arg1468Ter(p.R1468*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000294618 |
| Start | 11233298:11233300(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2621_2623delACC |
| AA Mutation | p.Tyr874del(p.Y874del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |