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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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549562 SNVs 1 of 54957 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP004020528859 chr5: 21488 TW1 Intergenic A G
heterozygote
MACSNP004020528866 chr5: 22565 TW1 Intergenic T C
homozygote
MACSNP004020528879 chr5: 23463 TW1 Intergenic G A
heterozygote
MACSNP004020528880 chr5: 23497 TW1 Intergenic A C
heterozygote
MACSNP004020528883 chr5: 23685 TW1 Intergenic A T
heterozygote
MACSNP004020528918 chr5: 27241 TW1 ENSMMUG00000032295: 5'UTR
 C T
heterozygote
MACSNP004020528945 chr5: 32695 TW1 ENSMMUG00000032295: Intron
 C A
heterozygote
MACSNP004020528971 chr5: 36072 TW1 ENSMMUG00000032295: Intron
 A T
homozygote
MACSNP004020528985 chr5: 37797 TW1 ENSMMUG00000032295: Intron
 C T
homozygote
MACSNP004020529031 chr5: 44088 TW1 ENSMMUG00000032295: Intron
 T G
homozygote

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