SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs193924780 | snp | A/G | | | intron-variant | EMB2771 | TAIR10 | 5:1653322 | TAAAACCAGGTAGAC[A/G]AAATGACCAAGGACA | 830439 |
rs346441944 | snp | A/T | | | intron-variant | EMB2771 | TAIR10 | 5:1641946 | CGTTTTACCTTGTCT[A/T]CTGCCGTCATTAAGG | 830439 |
rs346477629 | snp | G/T | | | intron-variant | EMB2771 | TAIR10 | 5:1645121 | TGCATATGCTTTGAT[G/T]CAAACGTGGCACAAA | 830439 |
rs346489424 | snp | A/G | | | intron-variant | EMB2771 | TAIR10 | 5:1643105 | TATTTCTTTCTTGTT[A/G]TCTCAACAGCACATA | 830439 |
rs346496337 | snp | C/G | | | intron-variant | EMB2771 | TAIR10 | 5:1643365 | GAAATACTTTGTCTT[C/G]GTTTTTTCAGGCAAG | 830439 |
rs346553868 | snp | A/G | | | synonymous-codon | EMB2771 | TAIR10 | 5:1651874 | TGTGTAGGTCATGGC[A/G]GGATCTGGAGACTTG | 830439 |
rs346601807 | snp | C/T | | | synonymous-codon | EMB2771 | TAIR10 | 5:1643796 | CGATGTTAAGCCTGA[C/T]ATAAGCTGGAGTGTG | 830439 |
rs346606875 | snp | A/C | | | missense | EMB2771 | TAIR10 | 5:1646212 | CGATTGGCTTAGAAA[A/C]CACTAAGATTGAGGA | 830439 |
rs346607380 | snp | C/G | | | intron-variant | EMB2771 | TAIR10 | 5:1646444 | ATCTTTGTAGCTATG[C/G]TCATGTTGCATTGTT | 830439 |
rs346677575 | snp | A/T | | | intron-variant | EMB2771 | TAIR10 | 5:1647641 | TTTGCATGAAGCAGC[A/T]ATTTCAAGACATAAA | 830439 |
rs346686908 | snp | G/T | | | intron-variant | EMB2771 | TAIR10 | 5:1648346 | GGATGTCTGCTGTAT[G/T]GAGCATCACGTTACT | 830439 |
rs346731582 | snp | A/T | | | intron-variant | EMB2771 | TAIR10 | 5:1646487 | ATAAGGTAACTTGTT[A/T]GCTTGTAGTGCACTC | 830439 |
rs346754327 | snp | A/T | | | intron-variant | EMB2771 | TAIR10 | 5:1648577 | GGTGTACCCTGGTGA[A/T]GTACTTTCTATTTTA | 830439 |
rs346772847 | snp | A/G | | | intron-variant | EMB2771 | TAIR10 | 5:1653165 | TCAGCCATTCTACCT[A/G]TTTGTTTCGTCCACG | 830439 |
rs346858713 | snp | C/G | | | intron-variant | EMB2771 | TAIR10 | 5:1650097 | TTCTCAGTGGTGCAT[C/G]TTTGATACAGTTTGG | 830439 |
rs346911083 | snp | G/T | | | intron-variant | EMB2771 | TAIR10 | 5:1641854 | TCTAGCTGAATTGCG[G/T]TTCGTTTCTGTACCT | 830439 |
rs346913234 | snp | A/T | | | intron-variant | EMB2771 | TAIR10 | 5:1647962 | TACACGATCCCACTA[A/T]TGTATATTTATCATC | 830439 |
rs346919057 | snp | C/T | | | missense | EMB2771 | TAIR10 | 5:1645780 | TCTGGTGTTTCTCTC[C/T]CGCTAAGACATGTAA | 830439 |
rs346929071 | snp | C/G | | | intron-variant | EMB2771 | TAIR10 | 5:1652676 | AGACATGCTAAGCTT[C/G]GAAGTTGGTTTCAAA | 830439 |
rs346960221 | snp | A/C | | | intron-variant | EMB2771 | TAIR10 | 5:1643612 | TATACTATTTTTTTT[A/C]CTGAAGTATTTACTA | 830439 |
rs346973785 | snp | A/G | | | intron-variant | EMB2771 | TAIR10 | 5:1652332 | TTATTGTTGAGCAGA[A/G]TCCTATACTTTTCTT | 830439 |
rs346980861 | snp | C/G | | | intron-variant | EMB2771 | TAIR10 | 5:1651639 | TCTGGTCATCTCTAT[C/G]TGAGCTTATATGTTT | 830439 |
rs346984812 | snp | C/T | | | intron-variant | EMB2771 | TAIR10 | 5:1651997 | GCAAAATGAAGGTTC[C/T]TTGATTTCATGTAAT | 830439 |
rs347001759 | snp | A/G | | | intron-variant | EMB2771 | TAIR10 | 5:1648329 | GATATATATATATAT[A/G]TGGATGTCTGCTGTA | 830439 |
rs347070370 | snp | G/T | | | synonymous-codon | EMB2771 | TAIR10 | 5:1643274 | TGACCGTCTACCTCT[G/T]ATGACGTCGTATAAC | 830439 |
rs347084934 | snp | C/T | | | intron-variant | EMB2771 | TAIR10 | 5:1653585 | GTTCTGATACACGTT[C/T]GTATGCTTTCTGTGA | 830439 |
rs347098970 | snp | C/G | | | missense | EMB2771 | TAIR10 | 5:1651531 | CTTAACTCCTACGCT[C/G]TCTATCTTTTGAATG | 830439 |
rs347119674 | snp | A/T | | | missense | EMB2771 | TAIR10 | 5:1645669 | TCAGGTGTCCCCTGT[A/T]ATATCGCGCCAGGAT | 830439 |
rs347210769 | snp | C/G | | | intron-variant | EMB2771 | TAIR10 | 5:1649746 | TATAGCGTTCTTCTT[C/G]TCATCAATCTCATTC | 830439 |
rs347339357 | snp | C/T | | | intron-variant | EMB2771 | TAIR10 | 5:1642009 | TCAAGTTTTCCCGTT[C/T]GAAAATCTATGGATT | 830439 |
rs347394961 | snp | G/T | | | intron-variant | EMB2771 | TAIR10 | 5:1649523 | TTACTGCAGAAGTGA[G/T]GATCAGAAAATCTGG | 830439 |