EOL2
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs346451751snpA/Gintron-variantEOL2TAIR105:23666494ATGTAGCTTCCGTCA[A/G]CTCCTGAAGAATTCA835968
rs346614770snpG/Tutr-variant-3-prime, intron-variantEOL2TAIR105:23665365CTTTACAGCATCCAT[G/T]TATAGAAGAAGAAAA835968
rs346664145snpC/TmissenseEOL2TAIR105:23666832TCACCAGTGGCTAAA[C/T]ACAGCCAAGCCCTCA835968
rs346852991snpC/TmissenseEOL2TAIR105:23667804GAAAGCGCTGCGATT[C/T]TCGACCTAACACACT835968
rs346920172snpC/GmissenseEOL2TAIR105:23666977ACAGTGTCGGGTCAA[C/G]TTCAGTGGCGGTTGC835968
rs347093576snpC/Gsynonymous-codonEOL2TAIR105:23665778GAAGAGTTAGTTACC[C/G]GCAGCTCGGTATCTG835968
rs347150604snpA/Csynonymous-codonEOL2TAIR105:23666822ACTCTCCCGGTCACC[A/C]GTGGCTAAATACAGC835968
rs347151881snpA/CmissenseEOL2TAIR105:23667632TAATTGAAGCAGCTC[A/C]AATACAGTTTCCACA835968
rs347346716snpC/GmissenseEOL2TAIR105:23668082TCTCAACCAAGCAGA[C/G]AAAACAACCTTACAA835968
rs347357072snpA/Tintron-variantEOL2TAIR105:23665709CATCAGCACTGCCAC[A/T]CATACGATCACTTCT835968
rs347446318snpC/Tsynonymous-codonEOL2TAIR105:23667095GTTCATGAGCCTGTA[C/T]GCCGAATACCTCTTC835968
Full records
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