Primary Site >> Stomach Cancer
Gene >> USP20
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315480 |
| Start | 129868350:129868350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768323864 |
| CDS Mutation | c.1036G>A |
| AA Mutation | p.Glu346Lys(p.E346K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315480 |
| Start | 129870496:129870496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370182930 |
| CDS Mutation | c.1609G>A |
| AA Mutation | p.Val537Ile(p.V537I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315480 |
| Start | 129875432:129875432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766157763 |
| CDS Mutation | c.2171C>T |
| AA Mutation | p.Ala724Val(p.A724V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315480 |
| Start | 129856320:129856320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181271773 |
| CDS Mutation | c.95C>T |
| AA Mutation | p.Ser32Leu(p.S32L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315480 |
| Start | 129874727:129874727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1892C>T |
| AA Mutation | p.Ser631Leu(p.S631L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315480 |
| Start | 129874598:129874598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762740870 |
| CDS Mutation | c.1763G>A |
| AA Mutation | p.Arg588His(p.R588H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315480 |
| Start | 129873730:129873730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1726C>A |
| AA Mutation | p.Leu576Met(p.L576M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315480 |
| Start | 129873733:129873733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778065634 |
| CDS Mutation | c.1729C>T |
| AA Mutation | p.Arg577Trp(p.R577W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315480 |
| Start | 129858488:129858488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs191133247 |
| CDS Mutation | c.220G>A |
| AA Mutation | p.Val74Met(p.V74M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315480 |
| Start | 129874673:129874673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142714756 |
| CDS Mutation | c.1838G>A |
| AA Mutation | p.Arg613His(p.R613H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315480 |
| Start | 129868337:129868337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758892167 |
| CDS Mutation | c.1023G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315480 |
| Start | 129874929:129874929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375361283 |
| CDS Mutation | c.2022C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |