AUR2
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs346592385snpA/Tutr-variant-3-primeAUR2TAIR102:11034812ATATAGAACTATGAA[A/T]TGGTCAGACTTTTTG817129
rs346704530snpG/Tintron-variantAUR2TAIR102:11035059TAGAGAGATTTACGA[G/T]GAATGCGAGTAGAAA817129
rs346769095snpC/Tintron-variantAUR2TAIR102:11034998CAACATCTGTTTGAT[C/T]AGAAAGTGTGAAAAT817129
rs346811403snpC/Gintron-variantAUR2TAIR102:11035191CTTTAATGTACATTC[C/G]ACTGACCAAACATCA817129
rs346836091snpC/Tsynonymous-codon, intron-variantAUR2TAIR102:11035666CAACAGATTTTCAGG[C/T]TTTATATCTCTGTGA817129
rs346846567snpG/Tintron-variant, synonymous-codonAUR2TAIR102:11035711ATGGCAATAGATGAG[G/T]GCTCTAGCCAATGAC817129
rs346915554snpA/Tsynonymous-codonAUR2TAIR102:11036293CTTTCCTCTACCAAG[A/T]GGCTTTCCGATATCG817129
rs346972598snpA/Gsynonymous-codonAUR2TAIR102:11036089TTCCCTTCGTAACTG[A/G]TGTTCAACTTGAGAT817129
rs346986509snpA/Cintron-variantAUR2TAIR102:11036527CCTCGCTGTAAACGA[A/C]TAAATCCACAATCAT817129
rs346988852snpA/Gintron-variantAUR2TAIR102:11035366AACGCTTTCCACTGT[A/G]AATCCAAAAGCAGAA817129
rs347069886snpG/Tintron-variantAUR2TAIR102:11035749ACTGCCACAATAAAC[G/T]TAAGGGTATGACTAC817129
rs347165783snpC/Tintron-variantAUR2TAIR102:11036219TTAATTCTGCTTGTT[C/T]AACATAATTGTGAAG817129
rs347224672snpA/Gsynonymous-codonAUR2TAIR102:11035840TCGACGTTCGCTGAA[A/G]TACTTGCACTTCTGA817129
rs347234978snpC/Gintron-variant, missenseAUR2TAIR102:11035718TAGATGAGGGCTCTA[C/G]CCAATGACGCAACAT817129
rs347367224snpA/Gintron-variantAUR2TAIR102:11036483AGCTCCTTAACACTA[A/G]TCCACGGATTTGTCA817129
rs347374934snpG/Tsynonymous-codonAUR2TAIR102:11036082TCTCTACTTCCCTTC[G/T]TAACTGGTGTTCAAC817129
rs347395255snpC/Tintron-variantAUR2TAIR102:11036362AGCCGCCTGATACAA[C/T]ATTATCACAAAGATT817129
Full records
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