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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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343285 SNVs 1 of 34329 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013065724322 chr17: 37946 TM2 Intergenic C A
homozygote
MACSNP013065724355 chr17: 38232 TM2 Intergenic C T
heterozygote
MACSNP013065724440 chr17: 39376 TM2 Intergenic A G
heterozygote
MACSNP013065724443 chr17: 39421 TM2 Intergenic C T
heterozygote
MACSNP013065724508 chr17: 40974 TM2 Intergenic G A
heterozygote
MACSNP013065724510 chr17: 40995 TM2 Intergenic A G
heterozygote
MACSNP013065724522 chr17: 41099 TM2 Intergenic G A
heterozygote
MACSNP013065724529 chr17: 41146 TM2 Intergenic T C
heterozygote
MACSNP013065724530 chr17: 41154 TM2 Intergenic C G
heterozygote
MACSNP013065724533 chr17: 41195 TM2 Intergenic C T
heterozygote

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