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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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1062041 SNVs 1 of 106205 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020020528810 chr5: 422 BM1 Intergenic A G
heterozygote
MACSNP020020528811 chr5: 439 BM1 Intergenic A G
heterozygote
MACSNP020020528815 chr5: 631 BM1 Intergenic G A
heterozygote
MACSNP020020528816 chr5: 652 BM1 Intergenic A C
heterozygote
MACSNP020020528817 chr5: 680 BM1 Intergenic A G
heterozygote
MACSNP020020528899 chr5: 25224 BM1 Intergenic T G
homozygote
MACSNP020020528900 chr5: 25393 BM1 Intergenic C T
homozygote
MACSNP020020528905 chr5: 25863 BM1 Intergenic A G
homozygote
MACSNP020020528916 chr5: 27071 BM1 ENSMMUG00000032295: 5'UTR
 G A
homozygote
MACSNP020020528935 chr5: 30465 BM1 ENSMMUG00000032295: Intron
 G A
homozygote

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