Bfar
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs8156609snpA/G00utr-variant-3-primeBfarRn_Celera10:1497312GTAGCACTTGGCATA[A/G]TTATACATGCTTTTA304709
rs13453608snpA/G0.3362980.234633missenseBfarRn_Celera10:1496378CTGGTGGTCAAGGAA[A/G]TCCGACGGCTGGAAA304709
rs106038820snpC/T0.2141580.247417intron-variant, utr-variant-5-primeBfar, RGD1305537Rn_Celera10:1469637AGAGGTCTGGTTGCA[C/T]GCGCTGGTGGGTAAA304709
rs197224422snpG/T00intron-variantBfarRn_Celera10:1485510TACAACCATTTCCAG[G/T]CATTTCCTGACTCCC304709
rs197302150snpG/T00missenseBfarRn_Celera10:1485083CTGTCTCCTTTCAGG[G/T]CATCCTGCTTGTGTA304709
rs197403385snpA/C/G/T00intron-variantBfar, RGD1305537Rn_Celera10:1465985AACCCAAAGTTAAGT[A/C/G/T]TTCAGAGTGAGGCTA304709
rs197674910snpA/C00intron-variantBfarRn_Celera10:1485263GAAGGTGAGGAATTA[A/C]AATCTGTCACACCAA304709
rs197755687snpG/T00intron-variantBfarRn_Celera10:1485363GCCTGGCAACTATCA[G/T]GCCACAAGGTGACAT304709
rs198025834snpC/G00intron-variantBfar, RGD1305537Rn_Celera10:1468943TACCAGATGGTCTTA[C/G]GCAACTCCTGCAAGA304709
rs198091826snpA/G00intron-variantBfarRn_Celera10:1485929TTGGAGCTCTTTGAA[A/G]AGTGCTGCTAAAGTC304709
rs198223259snpG/T00missenseBfarRn_Celera10:1485151GTGCACAAGGCTGTA[G/T]ACAAATGGACGACAG304709
rs198547581snpC/G00intron-variantBfar, RGD1305537Rn_Celera10:1468872AGGACTATTGCACTA[C/G]GAGAAAGTAAATCTA304709
rs198939916snpA/T00intron-variantBfarRn_Celera10:1485338CAGAGCTCTTGTGAG[A/T]TTGAGGCCAGCCTGG304709
rs198982654snpC/G00intron-variantBfarRn_Celera10:1485460AATCCTTTTCTTACA[C/G]AAGTGAATGTGTTTG304709
rs199042996snpG/T00intron-variantBfarRn_Celera10:1485301GTGGTGGTGCAAGCA[G/T]GCCTTTAATCTCAGA304709