TFCB
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs346481965snpA/Gintron-variant?TAIR103:3162902TAGCTTAGTCACTGC[A/G]GAGAAGTATTTGGGG820184
rs346556376snpA/Cintron-variant?TAIR103:3162646TAAATTCTCTACTAC[A/C]TGTAATCGGTGTCTC820184
rs346655664snpA/Cintron-variant?TAIR103:3162366TGTAGAGATTGCAAA[A/C]GGTTGGCTAATTTAG820184
rs346786018snpG/Tmissense?TAIR103:3163200TGCCAAGTTGAGCCT[G/T]GGGAGAAAAGAGGAA820184
rs346875105snpC/Gintron-variant?TAIR103:3162466ATGACATGGCTTCTT[C/G]TTTTATCATTTCATC820184
rs346948819snpA/Gintron-variant?TAIR103:3163791CAAGTTTGATATTAG[A/G]AGTCTGGAGTCGAAT820184
rs346989762snpC/Tmissense?TAIR103:3162292TTCTCAGTGATGATT[C/T]TAGACCTCTTGGTTT820184
rs347169066snpC/Tsynonymous-codon?TAIR103:3162251GGCTTTAGAGCTCTA[C/T]GATGACTCTGGCTCA820184
rs347195932snpA/Gintron-variant?TAIR103:3163409CTAGAACCTTGTGCT[A/G]GTATCACTTTAAGCG820184
rs347199560snpG/Tintron-variant?TAIR103:3161918AGTCGAATTTTTTTT[G/T]GATTTCATTGAGATA820184
rs347238596snpA/Gintron-variant?TAIR103:3163805GGAGTCTGGAGTCGA[A/G]TATGGGTTAGCTATA820184
rs347289033snpA/Gintron-variant?TAIR103:3162972TCTTCTTCCAATTTT[A/G]TCCTTTCAACAGACG820184
rs347382764snpC/Tintron-variant?TAIR103:3163136CTCTTTCTCAACTCG[C/T]TATGCTTCTAATTTA820184
rs347389360snpG/Tintron-variant?TAIR103:3162464ACATGACATGGCTTC[G/T]TGTTTTATCATTTCA820184
rs347431209snpC/Gintron-variant?TAIR103:3162726GTTTGATGGTTGTAT[C/G]TTCTTGTGTTCAAAT820184
Full records
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