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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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761207 SNVs 1 of 76121 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP009020528852 chr5: 21121 CE3 Intergenic T C
heterozygote
MACSNP009020528866 chr5: 22565 CE3 Intergenic T C
homozygote
MACSNP009020528875 chr5: 23394 CE3 Intergenic G A
homozygote
MACSNP009020528879 chr5: 23463 CE3 Intergenic G A
heterozygote
MACSNP009020528880 chr5: 23497 CE3 Intergenic A C
heterozygote
MACSNP009020528897 chr5: 24823 CE3 Intergenic G A
heterozygote
MACSNP009020528898 chr5: 24990 CE3 Intergenic C T
heterozygote
MACSNP009020528906 chr5: 25936 CE3 Intergenic A G
heterozygote
MACSNP009020528937 chr5: 30790 CE3 ENSMMUG00000032295: Intron
 C T
heterozygote
MACSNP009020528938 chr5: 30899 CE3 ENSMMUG00000032295: Intron
 C T
heterozygote

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