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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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300554 SNVs 1 of 30056 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP004050510057 chr12: 38443 TW1 ENSMMUG00000009617: Intron
 C G
homozygote
MACSNP004050510067 chr12: 39590 TW1 Intergenic G A
homozygote
MACSNP004050510074 chr12: 40777 TW1 Intergenic C T
heterozygote
MACSNP004050510076 chr12: 45676 TW1 Intergenic G A
heterozygote
MACSNP004050510078 chr12: 45993 TW1 Intergenic G A
heterozygote
MACSNP004050510079 chr12: 46019 TW1 Intergenic G C
heterozygote
MACSNP004050510084 chr12: 46617 TW1 Intergenic C T
heterozygote
MACSNP004050510088 chr12: 47142 TW1 Intergenic C A
heterozygote
MACSNP004050510089 chr12: 47162 TW1 Intergenic G T
homozygote
MACSNP004050510098 chr12: 47981 TW1 Intergenic G A
homozygote

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