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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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372568 SNVs 1 of 37257 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016065724298 chr17: 37654 SM2 Intergenic A G
homozygote
MACSNP016065724310 chr17: 37813 SM2 Intergenic T C
homozygote
MACSNP016065724313 chr17: 37841 SM2 Intergenic C T
homozygote
MACSNP016065724314 chr17: 37854 SM2 Intergenic G A
homozygote
MACSNP016065724316 chr17: 37873 SM2 Intergenic G A
homozygote
MACSNP016065724322 chr17: 37946 SM2 Intergenic C A
homozygote
MACSNP016065724330 chr17: 38006 SM2 Intergenic T C
homozygote
MACSNP016065724337 chr17: 38100 SM2 Intergenic G A
homozygote
MACSNP016065724351 chr17: 38201 SM2 Intergenic G C
homozygote
MACSNP016065724356 chr17: 38234 SM2 Intergenic G A
homozygote

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