| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346801279 | snp | G/T | | | missense | UBC13 | TAIR10 | 3:17097311 | AGACAAGCTTGTGAG[G/T]TCATGGCGGATTGTG | 823796 |
| rs347019324 | snp | A/G | | | synonymous-codon | UBC13 | TAIR10 | 3:17096599 | AATAGATATACAAAC[A/G]CGGCCATCGGGATAA | 823796 |
| rs347082377 | snp | C/T | | | intron-variant | UBC13 | TAIR10 | 3:17096280 | TCCAATGAGACAGTG[C/T]TAATCTGATGAGTTC | 823796 |
| rs347101343 | snp | G/T | | | synonymous-codon | UBC13 | TAIR10 | 3:17096364 | GTCGTTGGGACCAGA[G/T]AGCATTGATATAATA | 823796 |
| rs347245969 | snp | A/G | | | utr-variant-5-prime | UBC13 | TAIR10 | 3:17097317 | GCTTGTGAGTTCATG[A/G]CGGATTGTGAGAAAT | 823796 |
| rs347310957 | snp | A/T | | | utr-variant-5-prime | UBC13 | TAIR10 | 3:17097339 | GTGAGAAATCGAGCT[A/T]GAGCTTCCAGTGATC | 823796 |
| rs347348201 | snp | A/C | | | intron-variant | UBC13 | TAIR10 | 3:17096211 | TTCTGCAAGAGGAAA[A/C]CCCACAAGGAGAATG | 823796 |