At4g32990
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs346454878snpC/Gmissense?TAIR104:15920550TTGGTCACCGTCTGG[C/G]AAGTTTCGATGGCAA829436
rs346489325snpC/Tintron-variant?TAIR104:15922455TGCAGGGTAATCTTA[C/T]TCGTATGTTGGTACT829436
rs346501547snpC/Tsynonymous-codon?TAIR104:15920557CCGTCTGGGAAGTTT[C/T]GATGGCAATACTTGC829436
rs346562861snpA/Tmissense?TAIR104:15922040TTTGTGGACAGCGAC[A/T]GTGACTCTGTATGCC829436
rs346577284snpA/Gsynonymous-codon?TAIR104:15920602TGCTACTGACTCCGA[A/G]TCTGTCTCTGTTTTA829436
rs346609359snpG/Tintron-variant?TAIR104:15921011TTTCATGAATTGGTG[G/T]CATATCTATGCATAA829436
rs346631537snpA/Tintron-variant?TAIR104:15922285ACAGCCAAATTGAAA[A/T]GCTGGTCATCATTGT829436
rs346640566snpC/Gmissense?TAIR104:15920546TAGCTTGGTCACCGT[C/G]TGGGAAGTTTCGATG829436
rs346673697snpG/Tstop-gained?TAIR104:15921094TGAAGATGGTGATTA[G/T]AATTGTGTACAAACC829436
rs346675775snpA/Gintron-variant?TAIR104:15921911TTGCTGACCAATATT[A/G]ATTGTCTTCTATGTG829436
rs346678156snpC/Tsynonymous-codon?TAIR104:15920956CTCTTGCAGTTATGA[C/T]AACACTATCAAGGTT829436
rs346685562snpA/Tintron-variant?TAIR104:15922420TTCCTAAGGAGTAAT[A/T]GGCTAAATATGTAAA829436
rs346719355snpA/Gintron-variant?TAIR104:15921602AGATACATGCGGTTG[A/G]ATATTCTTCATTTGC829436
rs346734636snpC/Tintron-variant?TAIR104:15920476TAATGAACATGAAGC[C/T]TCGTGATTGGTCAGG829436
rs346774264snpA/Tmissense?TAIR104:15920583CTTGCGTTTGGGAAA[A/T]TTTTGCTACTGACTC829436
rs346782257snpC/Gintron-variant?TAIR104:15922140TTGTCCGGTTTACTT[C/G]TTGGCATATGCTCTG829436
rs346905930snpA/Gintron-variant?TAIR104:15921389TCTGTTAACATTTGG[A/G]TTGTCTGAACTTTGC829436
rs346979683snpA/Tmissense?TAIR104:15920841GGATTTGGGAAATAC[A/T]ACCAGAGGAGGACGA829436
rs347008935snpG/Tintron-variant?TAIR104:15921574TTATTGTATGGTCTA[G/T]AAGTTTGACATAAGA829436
rs347019682snpG/Tstop-gained?TAIR104:15921998GGTGTTATTGCTAGT[G/T]GAGCAGGCGATGATA829436
rs347037309snpA/Cintron-variant?TAIR104:15921809ACTATATTCCCATGC[A/C]AACCAAGAAGATGAT829436
rs347040931snpA/Gsynonymous-codon?TAIR104:15922640GGTTAAGATTTGGAA[A/G]CTTGCCTCGGAGCCA829436
rs347041247snpA/Cmissense?TAIR104:15920565GAAGTTTCGATGGCA[A/C]TACTTGCGTTTGGGA829436
rs347097233snpA/Tintron-variant?TAIR104:15920685ACTGAAATTTATTGT[A/T]GGGCTTTGATGTCCC829436
rs347109397snpG/Tintron-variant?TAIR104:15920683CAACTGAAATTTATT[G/T]TAGGGCTTTGATGTC829436
rs347120531snpG/Tmissense?TAIR104:15920290CTTGAAGGTCACACT[G/T]ATCGTGTTTGGAACG829436
rs347135100snpC/Gintron-variant?TAIR104:15922235GCTTTAGACTCTAGC[C/G]AGTGATTTTTCATTA829436
rs347202006snpA/Tintron-variant?TAIR104:15922279TTGTGTACAGCCAAA[A/T]TGAAAAGCTGGTCAT829436
rs347211002snpA/Gintron-variant?TAIR104:15920514GGAAGGCGCGCACAC[A/G]AGAAGTGTGAAGTCG829436
rs347256470snpA/Cintron-variant?TAIR104:15921017GAATTGGTGTCATAT[A/C]TATGCATAAGCATTT829436
rs347306744snpC/Gintron-variant?TAIR104:15922059ACTCTGTATGCCCTT[C/G]TCCCTTTTACCTATA829436
rs347312539snpC/Gmissense?TAIR104:15922592ATTGCAGAAGGAAAG[C/G]CGGTTGCTTGCCTCG829436
rs347325785snpG/Tmissense?TAIR104:15921298TTTAATGCTGCAGGG[G/T]ACAAGATGGTCACTT829436
rs347327697snpA/Gmissense?TAIR104:15922363GCACATGAAATGGAT[A/G]TAAATTCGGTCCAAT829436
rs347365936snpA/Cmissense?TAIR104:15921690AGGACTCATGTTTGT[A/C]CACTCTCTGGTTTTC829436
rs347425074snpA/Tintron-variant?TAIR104:15920502TCAGGCTGTTTTGGA[A/T]GGCGCGCACACAAGA829436
rs347426446snpA/Gintron-variant?TAIR104:15920627GTTTTACGGGTACTA[A/G]ATGTACTATCTCAAA829436
rs347427417snpA/Gintron-variant?TAIR104:15922270CAATATACCTTGTGT[A/G]CAGCCAAATTGAAAA829436
rs347473430snpA/Gmissense?TAIR104:15921420AGTGATGATCTAGCA[A/G]TGAAAATATGGAAGA829436