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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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435110 SNVs 1 of 43511 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP009060569676 chr15: 14047 CE3 Intergenic G A
heterozygote
MACSNP009060569688 chr15: 15466 CE3 Intergenic C T
heterozygote
MACSNP009060569697 chr15: 16844 CE3 Intergenic G A
heterozygote
MACSNP009060569730 chr15: 25805 CE3 ENSMMUG00000012546: CDS
 C A
heterozygote
MACSNP009060569741 chr15: 28282 CE3 Intergenic T C
heterozygote
MACSNP009060569874 chr15: 36360 CE3 Intergenic T C
heterozygote
MACSNP009060569936 chr15: 39548 CE3 Intergenic G A
heterozygote
MACSNP009060569943 chr15: 40734 CE3 Intergenic A G
heterozygote
MACSNP009060569944 chr15: 40741 CE3 Intergenic A C
heterozygote
MACSNP009060570037 chr15: 49281 CE3 Intergenic C T
heterozygote

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