Primary Site >> Stomach Cancer
Gene >> ZNF365
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000410046 |
| Start | 62666145:62666145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1237A>C |
| AA Mutation | p.Ser413Arg(p.S413R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395254 |
| Start | 62376220:62376220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.27C>A |
| AA Mutation | p.Ser9Arg(p.S9R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395254 |
| Start | 62376840:62376840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.647G>T |
| AA Mutation | p.Arg216Leu(p.R216L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395254 |
| Start | 62388461:62388461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547383793 |
| CDS Mutation | c.809G>A |
| AA Mutation | p.Arg270Gln(p.R270Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395254 |
| Start | 62376843:62376843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.650C>T |
| AA Mutation | p.Ala217Val(p.A217V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395254 |
| Start | 62376888:62376888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.695T>C |
| AA Mutation | p.Leu232Pro(p.L232P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395254 |
| Start | 62399726:62399726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1161C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395254 |
| Start | 62376862:62376862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150802191 |
| CDS Mutation | c.669C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395254 |
| Start | 62376577:62376577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.384C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000395254 |
| Start | 62399754:62399755(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1195_1196delAA |
| AA Mutation | p.Lys399AlafsTer32(p.K399Afs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000395254 |
| Start | 62399754:62399754(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs764105435 |
| CDS Mutation | c.1196delA |
| AA Mutation | p.Lys399SerfsTer6(p.K399Sfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |