| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346474787 | snp | C/T | | | intron-variant | UBC14 | TAIR10 | 3:20531962 | TGTTTTCCTCGTCTG[C/T]TGTTTATTCATAGTG | 824704 |
| rs346602342 | snp | A/T | | | missense, intron-variant | UBC14 | TAIR10 | 3:20532552 | TATAAGTCAGGACTT[A/T]GGAATACTCTGGAGG | 824704 |
| rs346654631 | snp | A/C | | | intron-variant | UBC14 | TAIR10 | 3:20532175 | TATCTCTTTCTCGAG[A/C]TTTTAGGATTTAGTC | 824704 |
| rs346656169 | snp | A/G | | | intron-variant | UBC14 | TAIR10 | 3:20532183 | TCTCGAGCTTTTAGG[A/G]TTTAGTCTTCTGATG | 824704 |
| rs346669662 | snp | A/G | | | synonymous-codon | UBC14 | TAIR10 | 3:20532802 | CGATGAGTCACCAGC[A/G]AATGTGGAAGCTGCA | 824704 |
| rs346891571 | snp | A/G | | | intron-variant | UBC14 | TAIR10 | 3:20531937 | CTCATTGGATAAAAC[A/G]TTAATGACTTGTTTT | 824704 |
| rs346957639 | snp | A/C | | | intron-variant, missense | UBC14 | TAIR10 | 3:20532511 | TGAGCTTATACAGTG[A/C]TTGCTTTTCAAATGT | 824704 |
| rs346976952 | snp | C/T | | | intron-variant | UBC14 | TAIR10 | 3:20531833 | GTCTTTTGCTTATTT[C/T]AATTGTGCATTGATT | 824704 |