At1g04790
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs346489844snpC/Tintron-variant?TAIR101:1347493AATGTTGTTAAGTAC[C/T]GTAGAATCATCCTTA839412
rs346494700snpC/Tmissense?TAIR101:1346144GAACAGGAACTAGCT[C/T]CTGAAACTGCATCTT839412
rs346545117snpC/Tintron-variant?TAIR101:1347853TTTCATATCGAAATT[C/T]TGTTACTAAAAGCTT839412
rs346620393snpA/Gmissense?TAIR101:1345706CGTGCTTCTGTAGGC[A/G]ATGCTTTGTTTAGGA839412
rs346704779snpC/Gmissense?TAIR101:1346717AGGGTCTTCCGGGGT[C/G]CCAGACGTGTTGAAA839412
rs346718563snpC/Tintron-variant?TAIR101:1347096TTTACCTGGTTCTTT[C/T]GATTTTCTGTGTTCA839412
rs346726969snpC/Tutr-variant-3-prime?TAIR101:1348386AGAAAGTTGATACTA[C/T]CACTTATTCACTTTA839412
rs346814854snpG/Tstop-gained?TAIR101:1345988TCTGTTCCTCATAGA[G/T]AAACAATTGACCTTT839412
rs346884635snpC/Tmissense?TAIR101:1345778GATCCATGTGCGCCT[C/T]GTGTAGAGAAAAATC839412
rs346913316snpC/Tmissense?TAIR101:1345520GATACTCCAGATAGA[C/T]CGGTACACCATAGAG839412
rs346983907snpA/Tintron-variant?TAIR101:1345236ATTTTCACTAGTCTG[A/T]TCCTCAGTTTTAGAT839412
rs347025053snpC/Tmissense?TAIR101:1346073TTTCTCCACATGAAA[C/T]AGCAGCTAGAGCTAG839412
rs347076966snpA/Gmissense?TAIR101:1346170ATCTTCGATTGGCAT[A/G]AGAGAGATTGTTCCT839412
rs347077524snpA/Gmissense?TAIR101:1345683GAACTGAGAGTGGAC[A/G]TCGCCCTCGTGCTTC839412
rs347271610snpG/Tmissense?TAIR101:1346699GATTCATCTCCTGAA[G/T]TAAGGGTCTTCCGGG839412
rs347288537snpA/Cintron-variant?TAIR101:1347126AGATGCGAGACTAAT[A/C]TTTATCAAACATGAA839412
rs347325016snpA/Gmissense?TAIR101:1346459GAGAGTAACACACGC[A/G]GAATTTGTAGTTCTG839412
rs347333772snpC/Gintron-variant?TAIR101:1347176GCACTTAAAAAGAAT[C/G]TGGCTTTAGGGATCA839412
rs347352120snpA/Gmissense?TAIR101:1346051AGATTGGTGAGACAT[A/G]GCTGCATTTCTCCAC839412
rs347398248snpG/Tsynonymous-codon?TAIR101:1346398GGGGTGGGTTAGTAC[G/T]CGTAACCGAAATTTA839412
Full records
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