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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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440106 SNVs 1 of 44011 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP012050510057 chr12: 38443 TM1 ENSMMUG00000009617: Intron
 C G
homozygote
MACSNP012050510067 chr12: 39590 TM1 Intergenic G A
homozygote
MACSNP012050510069 chr12: 40004 TM1 Intergenic A C
heterozygote
MACSNP012050510071 chr12: 40506 TM1 Intergenic C G
homozygote
MACSNP012050510072 chr12: 40601 TM1 Intergenic T C
homozygote
MACSNP012050510073 chr12: 40616 TM1 Intergenic G T
heterozygote
MACSNP012050510074 chr12: 40777 TM1 Intergenic C T
homozygote
MACSNP012050510082 chr12: 46233 TM1 Intergenic A G
homozygote
MACSNP012050510084 chr12: 46617 TM1 Intergenic C T
homozygote
MACSNP012050510098 chr12: 47981 TM1 Intergenic G A
homozygote

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