| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346514427 | snp | C/T | | | intron-variant | ? | TAIR10 | 3:6929055 | CATTTATGCGTTTCC[C/T]GATTGTGTTCATCAG | 821529 |
| rs346659930 | snp | C/G | | | intron-variant | ? | TAIR10 | 3:6929047 | ATGGATTGCATTTAT[C/G]CGTTTCCCGATTGTG | 821529 |
| rs346776186 | snp | C/T | | | intron-variant | ? | TAIR10 | 3:6926942 | GGGCTTTCTTTCTAA[C/T]TGCATTTGCAATGTT | 821529 |
| rs346989438 | snp | C/T | | | intron-variant | ? | TAIR10 | 3:6928942 | TCACGTTAGAAAAAC[C/T]GCCACAGCTCCTGAT | 821529 |
| rs347180120 | snp | A/T | | | missense | ? | TAIR10 | 3:6926665 | CAAGGGGTTGGAGAG[A/T]CGGCAGTTGCTGTGG | 821529 |
| rs347241501 | snp | A/G | | | synonymous-codon | ? | TAIR10 | 3:6928520 | TGCTGATACAATTGC[A/G]TCTTTGCCTTCAAAA | 821529 |
| rs347314713 | snp | C/T | | | utr-variant-3-prime | ? | TAIR10 | 3:6929466 | TCAAAGATTGGAACA[C/T]TCTCAAGCGTTTTTA | 821529 |
| rs347316463 | snp | G/T | | | missense | ? | TAIR10 | 3:6926580 | GATTAACGAGACTGA[G/T]GGACGGTTGCCGGAG | 821529 |
| rs347379831 | snp | C/G | | | intron-variant | ? | TAIR10 | 3:6929140 | AATTCATTAGGAAGA[C/G]TATCTAGAGTATGGT | 821529 |
| rs347411367 | snp | A/C | | | intron-variant | ? | TAIR10 | 3:6927824 | TTGTTTGTAGTTAAG[A/C]CAGTCACTGGAATAG | 821529 |
| rs347467594 | snp | G/T | | | intron-variant | ? | TAIR10 | 3:6927412 | AGGGGCGTTCTAAAA[G/T]AAATTTTGGATTATG | 821529 |