| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346488096 | snp | A/G | | | synonymous-codon | ? | TAIR10 | 5:26466910 | GTTAGACTCTCTGAG[A/G]CTTCTCTCTTTGCAC | 836756 |
| rs346618305 | snp | A/T | | | utr-variant-3-prime | ? | TAIR10 | 5:26468444 | AGCTTGGGTCGAAGT[A/T]AAAATGGTGGGCCGG | 836756 |
| rs346619036 | snp | C/G | | | intron-variant | ? | TAIR10 | 5:26467392 | TTATGTCTCTAGCAG[C/G]TTGATGGACCACCTG | 836756 |
| rs346703776 | snp | A/C | | | utr-variant-5-prime | ? | TAIR10 | 5:26466233 | TGTTAGGGCTTCTAT[A/C]CATCACCGGCGATAT | 836756 |
| rs346742687 | snp | A/T | | | intron-variant | ? | TAIR10 | 5:26467693 | CCAATAAATAAACTG[A/T]TTTATGTAACTCTTT | 836756 |
| rs346762647 | snp | A/T | | | utr-variant-3-prime | ? | TAIR10 | 5:26468433 | ATCTGACTGAGAGCT[A/T]GGGTCGAAGTTAAAA | 836756 |
| rs346927343 | snp | C/G | | | intron-variant | ? | TAIR10 | 5:26467217 | TAAAATTGACCATTT[C/G]GGTTAACCACAGGGT | 836756 |
| rs347126107 | snp | C/G | | | intron-variant | ? | TAIR10 | 5:26467694 | CAATAAATAAACTGG[C/G]TTATGTAACTCTTTT | 836756 |
| rs347318451 | snp | C/T | | | synonymous-codon | ? | TAIR10 | 5:26466589 | TATGGTGACAGCTAG[C/T]GACGATGACTCAATT | 836756 |
| rs347349732 | snp | A/C | | | intron-variant | ? | TAIR10 | 5:26467814 | GTTGTTTCAGGTAAC[A/C]TTGAGTTTTACCTGA | 836756 |
| rs347467593 | snp | A/T | | | missense | ? | TAIR10 | 5:26466569 | TTTCACAAAACTTCG[A/T]CTTGTATGGTGACAG | 836756 |