Filter SNVs Using Feature Selection

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710127 SNVs 1 of 71013 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011000000011 chr1: 9620 CE5 Intergenic C T
homozygote
MACSNP011000000021 chr1: 9800 CE5 Intergenic G C
homozygote
MACSNP011000000024 chr1: 9909 CE5 Intergenic T C
homozygote
MACSNP011000000028 chr1: 9932 CE5 Intergenic T C
homozygote
MACSNP011000000070 chr1: 10885 CE5 Intergenic T C
homozygote
MACSNP011000000098 chr1: 11493 CE5 Intergenic G A
homozygote
MACSNP011000000122 chr1: 12162 CE5 Intergenic A G
homozygote
MACSNP011000000141 chr1: 13635 CE5 Intergenic T C
homozygote
MACSNP011000000146 chr1: 13826 CE5 Intergenic C T
homozygote
MACSNP011000000156 chr1: 14054 CE5 Intergenic T C
homozygote