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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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769351 SNVs 1 of 76936 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP019000000010 chr1: 9596 LM1 Intergenic C A
homozygote
MACSNP019000000023 chr1: 9857 LM1 Intergenic T C
heterozygote
MACSNP019000000024 chr1: 9909 LM1 Intergenic T C
homozygote
MACSNP019000000030 chr1: 9964 LM1 Intergenic C T
homozygote
MACSNP019000000047 chr1: 10429 LM1 Intergenic T C
homozygote
MACSNP019000000056 chr1: 10569 LM1 Intergenic C T
homozygote
MACSNP019000000070 chr1: 10885 LM1 Intergenic T C
homozygote
MACSNP019000000076 chr1: 10945 LM1 Intergenic G A
homozygote
MACSNP019000000077 chr1: 10979 LM1 Intergenic G C
homozygote
MACSNP019000000081 chr1: 11053 LM1 Intergenic T C
homozygote

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