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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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432607 SNVs 1 of 43261 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020068733183 chr18: 310 BM1 Intergenic A G
homozygote
MACSNP020068733215 chr18: 895 BM1 Intergenic A G
homozygote
MACSNP020068733217 chr18: 931 BM1 Intergenic C T
homozygote
MACSNP020068733220 chr18: 1024 BM1 Intergenic T C
homozygote
MACSNP020068733224 chr18: 1167 BM1 Intergenic A G
heterozygote
MACSNP020068733229 chr18: 1451 BM1 Intergenic A G
homozygote
MACSNP020068733230 chr18: 1478 BM1 Intergenic A G
homozygote
MACSNP020068733231 chr18: 1505 BM1 Intergenic G A
homozygote
MACSNP020068733235 chr18: 1813 BM1 Intergenic G C
homozygote
MACSNP020068733244 chr18: 2051 BM1 Intergenic T C
homozygote

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