Primary Site >> Stomach Cancer
Gene >> USP42
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6145636:6145636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1111C>T |
| AA Mutation | p.His371Tyr(p.H371Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6154154:6154154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2600G>A |
| AA Mutation | p.Cys867Tyr(p.C867Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6156987:6156987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371531352 |
| CDS Mutation | c.3875G>A |
| AA Mutation | p.Arg1292His(p.R1292H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6139188:6139188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.650G>A |
| AA Mutation | p.Ser217Asn(p.S217N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6115431:6115431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.350G>A |
| AA Mutation | p.Gly117Asp(p.G117D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6111287:6111287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.154C>T |
| AA Mutation | p.Leu52Phe(p.L52F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6154120:6154120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2566A>G |
| AA Mutation | p.Ser856Gly(p.S856G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6149853:6149853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772525190 |
| CDS Mutation | c.1657G>A |
| AA Mutation | p.Val553Ile(p.V553I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6149668:6149668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754564754 |
| CDS Mutation | c.1472A>G |
| AA Mutation | p.Asn491Ser(p.N491S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6154082:6154082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748410824 |
| CDS Mutation | c.2528C>T |
| AA Mutation | p.Pro843Leu(p.P843L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6147852:6147852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1346C>T |
| AA Mutation | p.Pro449Leu(p.P449L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306177 |
| Start | 6147849:6147849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758322239 |
| CDS Mutation | c.1343C>T |
| AA Mutation | p.Ala448Val(p.A448V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306177 |
| Start | 6150170:6150170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1974C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306177 |
| Start | 6140942:6140942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546216572 |
| CDS Mutation | c.753A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306177 |
| Start | 6153948:6153948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554217282 |
| CDS Mutation | c.2394C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000306177 |
| Start | 6153997:6153997(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2447delC |
| AA Mutation | p.Pro816LeufsTer9(p.P816Lfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |