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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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179287 SNVs 1 of 17929 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006063857291 chr16: 845 JM2 Intergenic T C
homozygote
MACSNP006063857296 chr16: 966 JM2 Intergenic C T
homozygote
MACSNP006063857297 chr16: 997 JM2 Intergenic T C
homozygote
MACSNP006063857355 chr16: 3350 JM2 Intergenic C T
homozygote
MACSNP006063857356 chr16: 3357 JM2 Intergenic G A
homozygote
MACSNP006063857362 chr16: 3678 JM2 Intergenic T C
homozygote
MACSNP006063857366 chr16: 3735 JM2 Intergenic C T
homozygote
MACSNP006063857374 chr16: 4244 JM2 Intergenic A C
homozygote
MACSNP006063857380 chr16: 4515 JM2 Intergenic A G
homozygote
MACSNP006063857381 chr16: 4584 JM2 Intergenic G T
homozygote

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