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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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538645 SNVs 1 of 53865 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001005515268 chr2: 37287 CR1 Intergenic T G
homozygote
MACSNP001005515288 chr2: 38958 CR1 Intergenic A T
heterozygote
MACSNP001005515311 chr2: 41367 CR1 Intergenic T G
heterozygote
MACSNP001005515321 chr2: 42083 CR1 Intergenic T C
homozygote
MACSNP001005515323 chr2: 42145 CR1 Intergenic G A
heterozygote
MACSNP001005515324 chr2: 42589 CR1 Intergenic A G
heterozygote
MACSNP001005515325 chr2: 42784 CR1 Intergenic G T
heterozygote
MACSNP001005515327 chr2: 43402 CR1 Intergenic G A
heterozygote
MACSNP001005515330 chr2: 43844 CR1 Intergenic A T
heterozygote
MACSNP001005515331 chr2: 43955 CR1 Intergenic A T
homozygote

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