| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346435447 | snp | A/G | | | intron-variant | UBP8 | TAIR10 | 5:7295825 | AAAGTAAGCAAAAGT[A/G]ATTACGCAACTGTCA | 832263 |
| rs346561327 | snp | C/T | | | missense | UBP8 | TAIR10 | 5:7292862 | CGAGCCACATGATTT[C/T]GCCAATATTCATCAG | 832263 |
| rs346792693 | snp | A/C | | | intron-variant | UBP8 | TAIR10 | 5:7292600 | ACAGAACTCAAATCA[A/C]GAAGATAAAATTGCA | 832263 |
| rs346818083 | snp | A/C | | | intron-variant | UBP8 | TAIR10 | 5:7290792 | CCAAGGATCAGAGTA[A/C]TCCGAAGAATTAGTA | 832263 |
| rs346836946 | snp | A/T | | | intron-variant | UBP8 | TAIR10 | 5:7295792 | TAAAGCCTCAAAACA[A/T]AGCCTCTTAGGCTTA | 832263 |
| rs346970681 | snp | A/C | | | intron-variant | UBP8 | TAIR10 | 5:7296182 | TGGACGACATGAAAT[A/C]AAACGATTACGATAG | 832263 |
| rs346992483 | snp | A/C | | | intron-variant | UBP8 | TAIR10 | 5:7293967 | ACAGAATCAAAAGCA[A/C]ACGTATAAGTTGTAA | 832263 |
| rs347040196 | snp | A/G | | | intron-variant | UBP8 | TAIR10 | 5:7294299 | ATAGGTATTGAACTA[A/G]TGAAACATATAGAAG | 832263 |
| rs347069457 | snp | G/T | | | intron-variant | UBP8 | TAIR10 | 5:7294038 | TGACATGCATATCGT[G/T]TACACAGTACGTAAA | 832263 |
| rs347112659 | snp | C/T | | | intron-variant | UBP8 | TAIR10 | 5:7291802 | AGCATTTGAATACTA[C/T]GCAAACTTACTCTTC | 832263 |
| rs347138862 | snp | A/C | | | intron-variant | UBP8 | TAIR10 | 5:7296150 | TTCGCCGAATATTCC[A/C]TCAATCAAAAGGAAG | 832263 |
| rs347239687 | snp | A/C | | | missense | UBP8 | TAIR10 | 5:7291880 | TCTTTAACCGATACA[A/C]GACAAGTTTGTCACC | 832263 |
| rs347268626 | snp | C/T | | | intron-variant | UBP8 | TAIR10 | 5:7292392 | TATTAGGATCATTTT[C/T]GAACAAATGCACTGA | 832263 |
| rs347308815 | snp | A/C | | | intron-variant | UBP8 | TAIR10 | 5:7296120 | AAAATCAAACTCACT[A/C]GGATGCGATTCAGAT | 832263 |
| rs347334159 | snp | A/G | | | intron-variant | UBP8 | TAIR10 | 5:7290821 | TAAAGAGCAAGTCAG[A/G]CGCACAAAAAGCCCC | 832263 |
| rs347355142 | snp | A/T | | | intron-variant | UBP8 | TAIR10 | 5:7294882 | AACCCAAGCATATAT[A/T]CAAAAGGTACCAACT | 832263 |
| rs347371019 | snp | A/C | | | missense | UBP8 | TAIR10 | 5:7294773 | CCTCCAGCCGAGAAA[A/C]TTTTTACGCCTTTCT | 832263 |
| rs347384261 | snp | G/T | | | intron-variant | UBP8 | TAIR10 | 5:7295963 | CGAAATCACATTCAT[G/T]AGATTCTTCAGCTAG | 832263 |
| rs347385263 | snp | C/T | | | intron-variant | UBP8 | TAIR10 | 5:7295129 | CAAAAAGTTCCTAAT[C/T]TACCTCAGCCTCTTC | 832263 |