SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs371536649 | snp | C/T | | | missense | USP17L22 | GRCh38.p7 | 4:9268166 | CCGGGCACAAGCAGG[C/T]GGATCATCACTCTAA | 100287513 |
rs534562689 | snp | A/C | 0.00557542 | 0.0525036 | missense | USP17L22 | GRCh38.p7 | 4:9268510 | AAGAATGTGCAATAT[A/C]CTGAGTGCCTTGACA | 100287513 |
rs535525719 | snp | A/C | 0.000798403 | 0.0199641 | missense | USP17L22 | GRCh38.p7 | 4:9268559 | AGCAGAACACAGGAC[A/C]TCTCGTCTATGTCCT | 100287513 |
rs552690488 | snp | A/G | 0.00159617 | 0.0282053 | synonymous-codon | USP17L22 | GRCh38.p7 | 4:9268545 | GCCATACATGTCTCA[A/G]CAGAACACAGGACCT | 100287513 |
rs557118451 | snp | C/G | 0.000604047 | 0.0173683 | synonymous-codon | USP17L22 | GRCh38.p7 | 4:9268566 | CACAGGACCTCTCGT[C/G]TATGTCCTCTATGCT | 100287513 |
rs568086080 | snp | A/C | 0.00119189 | 0.0243829 | missense | USP17L22 | GRCh38.p7 | 4:9268558 | CAGCAGAACACAGGA[A/C]CTCTCGTCTATGTCC | 100287513 |
rs571066860 | snp | C/T | 0.00199481 | 0.0315187 | missense | USP17L22 | GRCh38.p7 | 4:9268475 | AGAGATTCTCCGATG[C/T]CACAGGCAACAAGAT | 100287513 |
rs575480218 | snp | A/T | 0.00438332 | 0.0466095 | missense | USP17L22 | GRCh38.p7 | 4:9268586 | TCCTCTATGCTGTGC[A/T]GGTCCACGCTGGGTG | 100287513 |
rs750154143 | snp | C/G | 0.00161812 | 0.0283979 | missense | USP17L22 | GRCh38.p7 | 4:9268522 | TATCCTGAGTGCCTT[C/G]ACATGCAGCCATACA | 100287513 |
rs753767503 | snp | A/G | 0.0209767 | 0.100241 | stop-gained | USP17L22 | GRCh38.p7 | 4:9268602 | GGTCCACGCTGGGTG[A/G]AGTTGTCACAACGGA | 100287513 |
rs754892206 | snp | G/T | 0.000608828 | 0.0174368 | missense | USP17L22 | GRCh38.p7 | 4:9268605 | CCACGCTGGGTGGAG[G/T]TGTCACAACGGACAT | 100287513 |
rs778958242 | snp | C/G/T | 0.00982459 | 0.0694265 | missense | USP17L22 | GRCh38.p7 | 4:9268609 | GCTGGGTGGAGTTGT[C/G/T]ACAACGGACATTACT | 100287513 |
rs780959064 | in-del | -/TA | 0.000736648 | 0.0191776 | frameshift-variant | USP17L22 | GRCh38.p7 | 4:9268630 | GGACATTACTTCTCT[-/TA]TGTCAAAGCTCAAGA | 100287513 |