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Filter SNVs Using Feature Selection

Chromosome chr1 chr2 chr3 chr4 chr5 chr6 chr7 chr8 chr9 chr10 chr11 chr12 chr13 chr14 chr15 chr16 chr17 chr18 chr19 chr20
Individual All CR1 CR2 CR3 TW1 JM1 JM2 CE1 CE2 CE3 CE4 CE5 TM1 TM2 AM1 SM1 SM2 PM1 PM2 LM1 BM1
Gene feature All CDS EXON 3'UTR INTRON 5'UTR Genotype All homozygote heterozygote Mutation All non-synonymous synonymous
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144498 SNVs 1 of 14450 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP014070912476 chr19: 27729 AM1 Intergenic G A
homozygote
MACSNP014070912481 chr19: 28057 AM1 Intergenic T C
heterozygote
MACSNP014070912496 chr19: 28345 AM1 Intergenic T C
homozygote
MACSNP014070912499 chr19: 28435 AM1 Intergenic G T
heterozygote
MACSNP014070912503 chr19: 28469 AM1 Intergenic C G
heterozygote
MACSNP014070912530 chr19: 29618 AM1 Intergenic T C
homozygote
MACSNP014070912535 chr19: 29749 AM1 Intergenic A G
heterozygote
MACSNP014070912544 chr19: 29985 AM1 Intergenic T C
heterozygote
MACSNP014070912549 chr19: 30045 AM1 Intergenic A G
homozygote
MACSNP014070912553 chr19: 30091 AM1 Intergenic A G
heterozygote

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