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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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420459 SNVs 1 of 42046 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016053619578 chr13: 1648 SM2 Intergenic A G
homozygote
MACSNP016053619581 chr13: 1702 SM2 Intergenic G T
homozygote
MACSNP016053619612 chr13: 8506 SM2 Intergenic G A
homozygote
MACSNP016053619714 chr13: 19993 SM2 Intergenic A G
homozygote
MACSNP016053619720 chr13: 20192 SM2 Intergenic A G
homozygote
MACSNP016053619742 chr13: 20838 SM2 Intergenic G A
homozygote
MACSNP016053619755 chr13: 21118 SM2 Intergenic C T
homozygote
MACSNP016053619839 chr13: 27882 SM2 Intergenic C T
homozygote
MACSNP016053619860 chr13: 28721 SM2 Intergenic G A
homozygote
MACSNP016053619875 chr13: 29070 SM2 Intergenic A C
homozygote

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