| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346568258 | snp | C/T | | | utr-variant-3-prime | UBP20 | TAIR10 | 4:9942766 | GCTAGCTACAAACTT[C/T]TTCTAGGTGTTATAA | 827513 |
| rs346576840 | snp | C/T | | | intron-variant | UBP20 | TAIR10 | 4:9941770 | TTTAGTAATTCTACT[C/T]GATCCGGGTGGTTTA | 827513 |
| rs346613745 | snp | A/G | | | missense | UBP20 | TAIR10 | 4:9940070 | CCAAATCGAGATCGC[A/G]GCGATGATGATGATA | 827513 |
| rs346637727 | snp | A/G | | | intron-variant | UBP20 | TAIR10 | 4:9942352 | CTGCAAGGTACTTCT[A/G]TTCTCTGATTACAGG | 827513 |
| rs346706245 | snp | C/G | | | synonymous-codon | UBP20 | TAIR10 | 4:9942195 | AGAGCTTTTGGACCC[C/G]CTTGATCCTGATGAT | 827513 |
| rs346789254 | snp | C/T | | | utr-variant-3-prime | UBP20 | TAIR10 | 4:9942743 | GTATCATGTCGACTT[C/T]CTTGATCGCTAGCTA | 827513 |
| rs346837572 | snp | C/G | | | missense | UBP20 | TAIR10 | 4:9942080 | ATTCTGCTGGAGTGT[C/G]TAACCAACATGTCAA | 827513 |
| rs346895748 | snp | C/G | | | missense | UBP20 | TAIR10 | 4:9942168 | TTCTAGTGGCGAGGA[C/G]TCTCCTATGGGAGAG | 827513 |
| rs346909277 | snp | G/T | | | missense | UBP20 | TAIR10 | 4:9941920 | GGAACTCGCTGGTTT[G/T]CTAGTGTCTATGAAG | 827513 |
| rs346932684 | snp | A/C | | | missense | UBP20 | TAIR10 | 4:9941221 | GCTGCAACTGTGACT[A/C]CGTCTCCGAGACATA | 827513 |
| rs347176695 | snp | A/G | | | intron-variant | UBP20 | TAIR10 | 4:9941771 | TTAGTAATTCTACTC[A/G]ATCCGGGTGGTTTAA | 827513 |
| rs347230769 | snp | G/T | | | missense | UBP20 | TAIR10 | 4:9942576 | AGCAATATCGCAGAT[G/T]CCATGGAAGCAGAAT | 827513 |
| rs347402283 | snp | A/G | | | synonymous-codon | UBP20 | TAIR10 | 4:9940631 | CAGATATGAAGTTCC[A/G]TGTCACTGTAAGACT | 827513 |
| rs347445961 | snp | C/G | | | missense | UBP20 | TAIR10 | 4:9942569 | ATCAATAAGCAATAT[C/G]GCAGATTCCATGGAA | 827513 |