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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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847736 SNVs 1 of 84774 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP018005515250 chr2: 35282 PM2 Intergenic T G
homozygote
MACSNP018005515259 chr2: 35947 PM2 Intergenic A T
homozygote
MACSNP018005515262 chr2: 36650 PM2 Intergenic T G
heterozygote
MACSNP018005515270 chr2: 37608 PM2 Intergenic T C
homozygote
MACSNP018005515279 chr2: 38356 PM2 Intergenic C A
homozygote
MACSNP018005515291 chr2: 39585 PM2 Intergenic A G
homozygote
MACSNP018005515292 chr2: 39593 PM2 Intergenic G C
homozygote
MACSNP018005515307 chr2: 41067 PM2 Intergenic C T
homozygote
MACSNP018005515321 chr2: 42083 PM2 Intergenic T C
heterozygote
MACSNP018005515333 chr2: 44101 PM2 Intergenic A G
homozygote

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