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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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406705 SNVs 1 of 40671 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016050510057 chr12: 38443 SM2 ENSMMUG00000009617: Intron
 C G
homozygote
MACSNP016050510067 chr12: 39590 SM2 Intergenic G A
homozygote
MACSNP016050510084 chr12: 46617 SM2 Intergenic C T
homozygote
MACSNP016050510088 chr12: 47142 SM2 Intergenic C A
heterozygote
MACSNP016050510091 chr12: 47192 SM2 Intergenic A T
heterozygote
MACSNP016050510098 chr12: 47981 SM2 Intergenic G A
homozygote
MACSNP016050510099 chr12: 48081 SM2 Intergenic A G
homozygote
MACSNP016050510104 chr12: 48427 SM2 Intergenic T G
homozygote
MACSNP016050510106 chr12: 48739 SM2 Intergenic C T
homozygote
MACSNP016050510112 chr12: 49145 SM2 Intergenic T C
homozygote

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