Primary Site >> Stomach Cancer
Gene >> YY1AP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295566 |
| Start | 155660564:155660564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749346586 |
| CDS Mutation | c.1484G>A |
| AA Mutation | p.Arg495Gln(p.R495Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295566 |
| Start | 155676695:155676695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.375G>T |
| AA Mutation | p.Lys125Asn(p.K125N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295566 |
| Start | 155659881:155659881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2167C>T |
| AA Mutation | p.His723Tyr(p.H723Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295566 |
| Start | 155660391:155660391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1657C>T |
| AA Mutation | p.Pro553Ser(p.P553S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295566 |
| Start | 155660688:155660688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1360C>T |
| AA Mutation | p.Arg454Cys(p.R454C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295566 |
| Start | 155676699:155676699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.371C>T |
| AA Mutation | p.Ala124Val(p.A124V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295566 |
| Start | 155660300:155660300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1748G>A |
| AA Mutation | p.Arg583Lys(p.R583K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295566 |
| Start | 155660137:155660137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397834368 |
| CDS Mutation | c.1911C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295566 |
| Start | 155680435:155680439(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.196_200delCTGAT |
| AA Mutation | p.Leu66GlyfsTer5(p.L66Gfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295566 |
| Start | 155660499:155660499(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1549delG |
| AA Mutation | p.Val517SerfsTer41(p.V517Sfs*41) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |