Primary Site >> Stomach Cancer
Gene >> KDM6A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377967 |
| Start | 45107448:45107448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3917T>C |
| AA Mutation | p.Leu1306Ser(p.L1306S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377967 |
| Start | 45078455:45078455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2888C>T |
| AA Mutation | p.Pro963Leu(p.P963L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377967 |
| Start | 45020708:45020708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.542C>T |
| AA Mutation | p.Thr181Ile(p.T181I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377967 |
| Start | 44873947:44873947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.185T>C |
| AA Mutation | p.Phe62Ser(p.F62S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377967 |
| Start | 45069616:45069616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1961C>G |
| AA Mutation | p.Pro654Arg(p.P654R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377967 |
| Start | 45083479:45083479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3304G>A |
| AA Mutation | p.Glu1102Lys(p.E1102K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377967 |
| Start | 45063540:45063540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1646G>C |
| AA Mutation | p.Arg549Thr(p.R549T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377967 |
| Start | 45069617:45069617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1962T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377967 |
| Start | 45020661:45020661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.495A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377967 |
| Start | 45063646:45063646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1752G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377967 |
| Start | 45083499:45083499(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3327delT |
| AA Mutation | p.Phe1109LeufsTer11(p.F1109Lfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377967 |
| Start | 45076707:45076707(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2717delA |
| AA Mutation | p.Asn906MetfsTer31(p.N906Mfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377967 |
| Start | 45079162:45079162(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2955delT |
| AA Mutation | p.Thr986LeufsTer13(p.T986Lfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377967 |
| Start | 45082743:45082743(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3241delA |
| AA Mutation | p.Thr1081ProfsTer2(p.T1081Pfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377967 |
| Start | 45089858:45089861(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3667_3670delGGCA |
| AA Mutation | p.Gly1223LeufsTer41(p.G1223Lfs*41) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377967 |
| Start | 45069731:45069731(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2080delG |
| AA Mutation | p.Ala694LeufsTer21(p.A694Lfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000377967 |
| Start | 45079164:45079235(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2957_3028delCTAAAACTTTGGTGGAAGCTAACAATGAACATATGGTAGAAGTGAGGACACAGTTGTTGCAGCCAGCAGATG |
| AA Mutation | p.Thr986_Glu1010delinsLys(p.T986_E1010delinsK) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000377967 |
| Start | 45083508:45083509(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs754641067 |
| CDS Mutation | c.3336_3338dupCGT |
| AA Mutation | p.Val1113dup(p.V1113dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |