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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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240448 SNVs 1 of 24045 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016063857297 chr16: 997 SM2 Intergenic T C
homozygote
MACSNP016063857312 chr16: 1342 SM2 Intergenic C T
homozygote
MACSNP016063857322 chr16: 1683 SM2 Intergenic A G
homozygote
MACSNP016063857331 chr16: 2080 SM2 Intergenic C A
homozygote
MACSNP016063857345 chr16: 2723 SM2 Intergenic G A
homozygote
MACSNP016063857363 chr16: 3687 SM2 Intergenic A G
homozygote
MACSNP016063857376 chr16: 4259 SM2 Intergenic G A
homozygote
MACSNP016063857396 chr16: 5464 SM2 Intergenic A G
homozygote
MACSNP016063857429 chr16: 6689 SM2 Intergenic G A
homozygote
MACSNP016063857432 chr16: 6782 SM2 Intergenic A C
homozygote

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