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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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132226 SNVs 1 of 13223 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002063857337 chr16: 2360 CR2 Intergenic A C
homozygote
MACSNP002063857343 chr16: 2639 CR2 Intergenic T C
homozygote
MACSNP002063857344 chr16: 2705 CR2 Intergenic T C
homozygote
MACSNP002063857406 chr16: 5802 CR2 Intergenic C T
homozygote
MACSNP002063857408 chr16: 5811 CR2 Intergenic G A
homozygote
MACSNP002063857437 chr16: 7138 CR2 Intergenic G A
homozygote
MACSNP002063857441 chr16: 7267 CR2 Intergenic A G
homozygote
MACSNP002063857478 chr16: 8949 CR2 Intergenic G T
homozygote
MACSNP002063857489 chr16: 9559 CR2 Intergenic G C
homozygote
MACSNP002063857493 chr16: 9723 CR2 Intergenic G A
homozygote

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