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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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536518 SNVs 1 of 53652 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017060569760 chr15: 32023 PM1 Intergenic A T
heterozygote
MACSNP017060569762 chr15: 32201 PM1 Intergenic A C
homozygote
MACSNP017060569763 chr15: 32212 PM1 Intergenic C T
heterozygote
MACSNP017060569764 chr15: 32256 PM1 Intergenic G C
heterozygote
MACSNP017060569765 chr15: 32286 PM1 Intergenic A C
homozygote
MACSNP017060569770 chr15: 32459 PM1 Intergenic C T
heterozygote
MACSNP017060569775 chr15: 32523 PM1 Intergenic C T
heterozygote
MACSNP017060569782 chr15: 32616 PM1 Intergenic A G
homozygote
MACSNP017060569784 chr15: 32697 PM1 Intergenic C A
heterozygote
MACSNP017060569792 chr15: 33049 PM1 Intergenic G A
heterozygote

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