Filter SNVs Using Feature Selection

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472839 SNVs 1 of 47284 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010056871533 chr14: 3954 CE4 Intergenic A G
homozygote
MACSNP010056871551 chr14: 4684 CE4 Intergenic A T
homozygote
MACSNP010056871553 chr14: 4779 CE4 Intergenic C T
homozygote
MACSNP010056871562 chr14: 5017 CE4 Intergenic C G
homozygote
MACSNP010056871567 chr14: 5338 CE4 Intergenic T C
homozygote
MACSNP010056871580 chr14: 5697 CE4 Intergenic A T
homozygote
MACSNP010056871581 chr14: 5726 CE4 Intergenic T C
homozygote
MACSNP010056871604 chr14: 6463 CE4 Intergenic T C
homozygote
MACSNP010056871612 chr14: 6740 CE4 Intergenic A G
homozygote
MACSNP010056871623 chr14: 7074 CE4 Intergenic C A
homozygote