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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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361930 SNVs 1 of 36193 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020063857292 chr16: 884 BM1 Intergenic C T
homozygote
MACSNP020063857293 chr16: 913 BM1 Intergenic G A
homozygote
MACSNP020063857298 chr16: 1026 BM1 Intergenic G A
homozygote
MACSNP020063857300 chr16: 1072 BM1 Intergenic G T
homozygote
MACSNP020063857303 chr16: 1128 BM1 Intergenic A C
homozygote
MACSNP020063857307 chr16: 1204 BM1 Intergenic A G
homozygote
MACSNP020063857308 chr16: 1232 BM1 Intergenic A C
homozygote
MACSNP020063857309 chr16: 1242 BM1 Intergenic A C
homozygote
MACSNP020063857313 chr16: 1354 BM1 Intergenic T G
homozygote
MACSNP020063857314 chr16: 1362 BM1 Intergenic G A
homozygote

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