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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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455362 SNVs 1 of 45537 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP014050510057 chr12: 38443 AM1 ENSMMUG00000009617: Intron
 C G
homozygote
MACSNP014050510067 chr12: 39590 AM1 Intergenic G A
homozygote
MACSNP014050510068 chr12: 39619 AM1 Intergenic C T
heterozygote
MACSNP014050510071 chr12: 40506 AM1 Intergenic C G
homozygote
MACSNP014050510072 chr12: 40601 AM1 Intergenic T C
homozygote
MACSNP014050510074 chr12: 40777 AM1 Intergenic C T
homozygote
MACSNP014050510075 chr12: 40890 AM1 Intergenic C T
heterozygote
MACSNP014050510081 chr12: 46115 AM1 Intergenic G A
heterozygote
MACSNP014050510084 chr12: 46617 AM1 Intergenic C T
homozygote
MACSNP014050510088 chr12: 47142 AM1 Intergenic C A
heterozygote

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