Primary Site >> Stomach Cancer
Gene >> NCOA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24705104:24705104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.968C>T |
| AA Mutation | p.Ala323Val(p.A323V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24742120:24742120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3640G>C |
| AA Mutation | p.Gly1214Arg(p.G1214R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24705121:24705121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.985A>G |
| AA Mutation | p.Arg329Gly(p.R329G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24751991:24751991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3716C>T |
| AA Mutation | p.Pro1239Leu(p.P1239L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24665904:24665904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.245G>T |
| AA Mutation | p.Arg82Ile(p.R82I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24705098:24705098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962G>A |
| AA Mutation | p.Gly321Asp(p.G321D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24706693:24706693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1223C>T |
| AA Mutation | p.Pro408Leu(p.P408L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24741884:24741884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3404T>A |
| AA Mutation | p.Met1135Lys(p.M1135K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24742172:24742172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3692A>G |
| AA Mutation | p.Gln1231Arg(p.Q1231R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24741964:24741964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3484G>A |
| AA Mutation | p.Gly1162Ser(p.G1162S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24758005:24758005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770279405 |
| CDS Mutation | c.3914C>T |
| AA Mutation | p.Thr1305Met(p.T1305M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24739490:24739490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3260G>A |
| AA Mutation | p.Gly1087Asp(p.G1087D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24707872:24707872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2402T>G |
| AA Mutation | p.Leu801Arg(p.L801R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24707710:24707710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2240A>G |
| AA Mutation | p.Gln747Arg(p.Q747R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24705200:24705200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1064A>C |
| AA Mutation | p.Gln355Pro(p.Q355P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24706598:24706598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1128C>A |
| AA Mutation | p.Asp376Glu(p.D376E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24665804:24665804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.145T>A |
| AA Mutation | p.Leu49Ile(p.L49I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24706728:24706728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754730103 |
| CDS Mutation | c.1258C>T |
| AA Mutation | p.Arg420Cys(p.R420C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348332 |
| Start | 24741815:24741815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3335G>A |
| AA Mutation | p.Arg1112His(p.R1112H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348332 |
| Start | 24706796:24706796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1326A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348332 |
| Start | 24706985:24706985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1515C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348332 |
| Start | 24658743:24658743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769344189 |
| CDS Mutation | c.66G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348332 |
| Start | 24707633:24707633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2163G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348332 |
| Start | 24705153:24705153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766755612 |
| CDS Mutation | c.1017C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348332 |
| Start | 24711029:24711029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757335592 |
| CDS Mutation | c.2517G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000348332 |
| Start | 24768342:24768342(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4282delC |
| AA Mutation | p.Gln1428ArgfsTer12(p.Q1428Rfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000348332 |
| Start | 24739516:24739516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3286C>T |
| AA Mutation | p.Gln1096Ter(p.Q1096*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |