Primary Site >> Stomach Cancer
Gene >> UGP2
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000337130 |
| Start | 63857935:63857935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781014998 |
| CDS Mutation | c.254C>T |
| AA Mutation | p.Ser85Leu(p.S85L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337130 |
| Start | 63884062:63884062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.544C>T |
| AA Mutation | p.Arg182Cys(p.R182C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337130 |
| Start | 63885856:63885856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.843A>C |
| AA Mutation | p.Glu281Asp(p.E281D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337130 |
| Start | 63887608:63887608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1278A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000337130 |
| Start | 63884032:63884032(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.520delA |
| AA Mutation | p.Ile174TyrfsTer10(p.I174Yfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000337130 |
| Start | 63884031:63884032(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.519_520dupAA |
| AA Mutation | p.Ile174LysfsTer11(p.I174Kfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000337130 |
| Start | 63884031:63884032(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs763972594 |
| CDS Mutation | c.520dupA |
| AA Mutation | p.Ile174AsnfsTer24(p.I174Nfs*24) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000337130 |
| Start | 63882651:63882654(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.441+3_441+6delGAGT |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |