| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346466015 | snp | A/G | | | intron-variant | UBP16 | TAIR10 | 4:12681840 | GATATATGCAACAAA[A/G]TTTGCTCAATTTCAG | 828558 |
| rs346577526 | snp | A/G | | | synonymous-codon | UBP16 | TAIR10 | 4:12683139 | ATCACTCACACGTTC[A/G]GCTGATCCAAGAGCC | 828558 |
| rs346710657 | snp | A/G | | | intron-variant | UBP16 | TAIR10 | 4:12680213 | GTATGATGCAGATAT[A/G]TGGATGATGACGAGA | 828558 |
| rs346852821 | snp | C/T | | | intron-variant | UBP16 | TAIR10 | 4:12684154 | ATCACTCCAATTCAT[C/T]ACGTCTCAGCAGAGA | 828558 |
| rs346920021 | snp | C/T | | | synonymous-codon | UBP16 | TAIR10 | 4:12681425 | ACATCTGTATTTGTT[C/T]TCTCCATCCAATATC | 828558 |
| rs346927434 | snp | A/T | | | intron-variant | UBP16 | TAIR10 | 4:12681789 | TGCAAATTGCAAGGA[A/T]AATGAAATTAACACA | 828558 |
| rs346961226 | snp | C/T | | | missense | UBP16 | TAIR10 | 4:12683596 | TCTGCAATATCTCCA[C/T]TCCCATCTTCAGGAG | 828558 |
| rs346964589 | snp | A/G | | | intron-variant | UBP16 | TAIR10 | 4:12680250 | CAGTCAATGAGTAGA[A/G]GCCAAAACATTTTCT | 828558 |
| rs346998255 | snp | A/C | | | missense | UBP16 | TAIR10 | 4:12681709 | ATCTTCTAATTTGCT[A/C]CTCTTGGTCATATCA | 828558 |
| rs347005320 | snp | G/T | | | intron-variant | UBP16 | TAIR10 | 4:12680225 | TATATGGATGATGAC[G/T]AGAAGAGACCAGTCA | 828558 |
| rs347022745 | snp | A/C | | | synonymous-codon | UBP16 | TAIR10 | 4:12681905 | TTCTTCCTTGCCATT[A/C]CCAAGAAAGATTCCA | 828558 |
| rs347130859 | snp | A/G | | | missense | UBP16 | TAIR10 | 4:12683204 | CAGCTGATACTGGAT[A/G]CCTATCCGTAACTAA | 828558 |
| rs347155329 | snp | A/G | | | missense | UBP16 | TAIR10 | 4:12683626 | GATCTGGCACGATTA[A/G]ATAATAGTGATTCCC | 828558 |
| rs347184974 | snp | A/T | | | synonymous-codon | UBP16 | TAIR10 | 4:12681884 | CCTAAGGAATTCATG[A/T]GCATCTTCTTCCTTG | 828558 |
| rs347288597 | snp | A/G | | | intron-variant | UBP16 | TAIR10 | 4:12681185 | TTGCAGCTGGTCGTG[A/G]AATCTAGGTATTGTA | 828558 |