At4g11860
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs346441295snpA/Gintron-variant?TAIR104:7135824GCAGCTCTAACCACA[A/G]TGGCATGCATGTATG826793
rs346467343snpA/Tintron-variant?TAIR104:7135806TGAACTAGAGCAAAG[A/T]GAGCAGCTCTAACCA826793
rs346501010snpC/Tintron-variant?TAIR104:7134822TGCAGATCAGAACTG[C/T]ATAGTACCATGGGAA826793
rs346518139snpC/Tmissense?TAIR104:7137731TGAGTCTGTCGACCA[C/T]GAGGGACATCAATCT826793
rs346539397snpC/Tintron-variant?TAIR104:7137868GTTAATTGATCTAAG[C/T]ATTATTAAGCACACT826793
rs346569686snpC/Tintron-variant?TAIR104:7137283ATTTAATTATTTACG[C/T]GCAGACAGAGCCATT826793
rs346597578snpA/Gintron-variant?TAIR104:7137117TCCATCTTAAAACGA[A/G]CCAAACAATGGATAA826793
rs346640069snpC/Tsynonymous-codon?TAIR104:7136807ATCATCAAAAGATCT[C/T]GTTTTCGAAAGACAA826793
rs346644785snpC/Tmissense?TAIR104:7136521TCGTTGTCGGAAATT[C/T]CCCAACTTTGATCAT826793
rs346678251snpA/Gsynonymous-codon?TAIR104:7135995TGACTCACCTTCATA[A/G]ACGGGTTCTTTGTCT826793
rs346698448snpC/Tsynonymous-codon?TAIR104:7136642ATCTGAAAATGTGAA[C/T]GCAGAATCTTGATTG826793
rs346701430snpA/C/Gintron-variant?TAIR104:7137916ACTTGTCATTTCTAC[A/C/G]AGAAGCTCAAGCTAA826793
rs346713927snpC/Tsynonymous-codon?TAIR104:7138173CATACAAATGGCTAA[C/T]AAAGGACAAGGTCCA826793
rs346744872snpC/Tsynonymous-codon?TAIR104:7138347CGGAGATTCTGAAGA[C/T]GAAGCGGTCGCCATT826793
rs346758100snpC/Tintron-variant?TAIR104:7134336GCTCCTTGGTACCTG[C/T]AATGGTCAGTACAAT826793
rs346782425snpA/Gintron-variant?TAIR104:7134495TAGTCGGTAAAGTAT[A/G]TGGACAGAAAACAAA826793
rs346793314snpA/Tintron-variant?TAIR104:7137866GTGTTAATTGATCTA[A/T]GTATTATTAAGCACA826793
rs346802752snpC/Tintron-variant?TAIR104:7135679ATGAATAAGATCACG[C/T]ACCCACAAAAGGTTA826793
rs346819191snpA/Gsynonymous-codon?TAIR104:7136963ATTATACGATTTGCT[A/G]CCAATTGCATTAGCT826793
rs346865156snpC/G/Tsynonymous-codon?TAIR104:7138281CGTAGTAGTTTCCTT[C/G/T]GGTAAATCTTGCTGC826793
rs346873786snpA/Gsynonymous-codon?TAIR104:7134294GCCGTCGTGTCTCGA[A/G]GACGCAGCTGATGAT826793
rs346912006snpC/Gmissense?TAIR104:7136317CATCAGACTTGAGTA[C/G]ACTCTCAGAACTGCT826793
rs346944876snpA/Cintron-variant?TAIR104:7138009CAAGCAAACCTAACA[A/C]CGATTCTTCAATTTC826793
rs346946059snpA/Csynonymous-codon?TAIR104:7137771AACCTCATAACAGTC[A/C]GGATTTAGATTCAAG826793
rs346973008snpC/Tmissense?TAIR104:7136562TTTTCTGATGCTTTA[C/T]CATCATCAGTTTTGA826793
rs347054918snpC/Gsynonymous-codon?TAIR104:7134991TACATTGTTGATGCT[C/G]GCAAGATAATCCTGT826793
rs347073734snpC/Tsynonymous-codon?TAIR104:7136954CATAAGAGCATTATA[C/T]GATTTGCTACCAATT826793
rs347090241snpG/Tintron-variant?TAIR104:7137905CAAATTCTCACACTT[G/T]TCATTTCTACGAGAA826793
rs347152937snpC/Tsynonymous-codon?TAIR104:7135980CCTTTTACCAAGAAG[C/T]GACTCACCTTCATAA826793
rs347175990snpA/Gintron-variant?TAIR104:7134451TTATCGATGTTTTAC[A/G]CTCGCAATTGGTACT826793
rs347182459snpA/Gsynonymous-codon?TAIR104:7138175TACAAATGGCTAACA[A/G]AGGACAAGGTCCATT826793
rs347187743snpA/Csynonymous-codon?TAIR104:7137804GTTTCTCAAGAGAAG[A/C]ACATTACCTGTTTCA826793
rs347229708snpA/C/Tsynonymous-codon?TAIR104:7136942AACTAGCTCACCCAT[A/C/T]AGAGCATTATACGAT826793
rs347231035snpA/Gintron-variant?TAIR104:7138125TACGATCTGAATGAA[A/G]TTTTATGAGGACGAA826793
rs347238152snpC/Tintron-variant?TAIR104:7135491ATTCAAAGATGGAAA[C/T]AACCGCAAACTAAAC826793
rs347242292snpG/Tintron-variant?TAIR104:7134597ATATTGTTGCAATGT[G/T]CAGGTCACACGGTAA826793
rs347282596snpC/Tutr-variant-5-prime?TAIR104:7138365AGCGGTCGCCATTGA[C/T]GATGATGATATCAAC826793
rs347285352snpA/Tintron-variant?TAIR104:7137947CAACAAAATCTGATG[A/T]TCGGTACACTAACCA826793
rs347314541snpC/Tintron-variant?TAIR104:7137816AAGCACATTACCTGT[C/T]TCATCCCAAAATCAA826793
rs347320649snpA/Gsynonymous-codon?TAIR104:7134970GACATCTATGCCTGC[A/G]TCCGCTACATTGTTG826793
rs347384929snpC/Tintron-variant?TAIR104:7134477GTACTTGTAAACTCA[C/T]CTTAGTCGGTAAAGT826793
rs347387502snpG/Tintron-variant?TAIR104:7135839ATGGCATGCATGTAT[G/T]AGTTTCCGAAAATGT826793
rs347415150snpC/Tsynonymous-codon?TAIR104:7134291TTTGCCGTCGTGTCT[C/T]GAAGACGCAGCTGAT826793
rs347430807snpC/Gintron-variant?TAIR104:7134413ATTATATTCAATGAG[C/G]TTCTGATTACGGTGT826793
rs347446426snpA/Cintron-variant?TAIR104:7137931GAGAAGCTCAAGCTA[A/C]CAACAAAATCTGATG826793
rs347477941snpA/Cintron-variant?TAIR104:7136272CAACTAAGGAAGAGT[A/C]AAAAAAACTACCTGG826793
Full records
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