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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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515874 SNVs 1 of 51588 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017050510057 chr12: 38443 PM1 ENSMMUG00000009617: Intron
 C G
homozygote
MACSNP017050510070 chr12: 40345 PM1 Intergenic G A
heterozygote
MACSNP017050510074 chr12: 40777 PM1 Intergenic C T
homozygote
MACSNP017050510077 chr12: 45712 PM1 Intergenic G T
heterozygote
MACSNP017050510084 chr12: 46617 PM1 Intergenic C T
homozygote
MACSNP017050510087 chr12: 47087 PM1 Intergenic G A
heterozygote
MACSNP017050510093 chr12: 47314 PM1 Intergenic C T
heterozygote
MACSNP017050510098 chr12: 47981 PM1 Intergenic G A
homozygote
MACSNP017050510102 chr12: 48222 PM1 Intergenic T C
homozygote
MACSNP017050510104 chr12: 48427 PM1 Intergenic T G
homozygote

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