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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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965450 SNVs 1 of 96545 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020015522760 chr4: 17341 BM1 Intergenic A G
homozygote
MACSNP020015522762 chr4: 17441 BM1 Intergenic C T
homozygote
MACSNP020015522763 chr4: 17469 BM1 Intergenic G A
homozygote
MACSNP020015522789 chr4: 18360 BM1 Intergenic T C
homozygote
MACSNP020015522793 chr4: 18481 BM1 Intergenic A G
homozygote
MACSNP020015522806 chr4: 19055 BM1 Intergenic C T
homozygote
MACSNP020015522826 chr4: 19818 BM1 Intergenic G T
homozygote
MACSNP020015522829 chr4: 19918 BM1 Intergenic T C
homozygote
MACSNP020015522832 chr4: 19957 BM1 Intergenic G T
homozygote
MACSNP020015522835 chr4: 20105 BM1 Intergenic G A
homozygote

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