Primary Site >> Stomach Cancer
Gene >> NCOA3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371998 |
| Start | 47637738:47637738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2467C>T |
| AA Mutation | p.His823Tyr(p.H823Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371998 |
| Start | 47635344:47635344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1135A>G |
| AA Mutation | p.Asn379Asp(p.N379D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371998 |
| Start | 47652412:47652412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3953G>A |
| AA Mutation | p.Gly1318Glu(p.G1318E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371998 |
| Start | 47635689:47635689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1480T>C |
| AA Mutation | p.Ser494Pro(p.S494P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371998 |
| Start | 47625419:47625419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.295G>A |
| AA Mutation | p.Asp99Asn(p.D99N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371998 |
| Start | 47636707:47636707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2321T>G |
| AA Mutation | p.Ile774Ser(p.I774S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371998 |
| Start | 47635552:47635552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1343T>C |
| AA Mutation | p.Met448Thr(p.M448T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371998 |
| Start | 47639760:47639760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762194641 |
| CDS Mutation | c.2891G>A |
| AA Mutation | p.Arg964Gln(p.R964Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371998 |
| Start | 47647287:47647287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146235035 |
| CDS Mutation | c.3467G>A |
| AA Mutation | p.Arg1156Gln(p.R1156Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371998 |
| Start | 47639752:47639752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2883G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371998 |
| Start | 47636540:47636540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371484815 |
| CDS Mutation | c.2154C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371998 |
| Start | 47639800:47639800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2931G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371998 |
| Start | 47636459:47636459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2073T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371998 |
| Start | 47651101:47651101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3771G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371998 |
| Start | 47639045:47639045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2550T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371998 |
| Start | 47635421:47635421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369152989 |
| CDS Mutation | c.1212G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371998 |
| Start | 47636241:47636241(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1860delA |
| AA Mutation | p.Lys620AsnfsTer18(p.K620Nfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371998 |
| Start | 47635604:47635604(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1400delC |
| AA Mutation | p.Pro467HisfsTer15(p.P467Hfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000371998 |
| Start | 47625479:47625479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.355C>T |
| AA Mutation | p.Gln119Ter(p.Q119*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000371998 |
| Start | 47622293:47622293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762111371 |
| CDS Mutation | c.46C>T |
| AA Mutation | p.Arg16Ter(p.R16*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000371998 |
| Start | 47642313:47642315(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3181_3183delCTC |
| AA Mutation | p.Leu1061del(p.L1061del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000371998 |
| Start | 47635996:47635997(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1612_1620dupTTATCTACT |
| AA Mutation | p.Thr540_Ser542dup(p.T540_S542dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |