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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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774113 SNVs 1 of 77412 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017031370844 chr7: 10473 PM1 Intergenic C G
homozygote
MACSNP017031370936 chr7: 25961 PM1 Intergenic G A
homozygote
MACSNP017031370939 chr7: 26343 PM1 Intergenic A G
homozygote
MACSNP017031370989 chr7: 29282 PM1 Intergenic G T
heterozygote
MACSNP017031370991 chr7: 29394 PM1 Intergenic C G
heterozygote
MACSNP017031370992 chr7: 29412 PM1 Intergenic C T
homozygote
MACSNP017031370997 chr7: 29460 PM1 Intergenic G A
heterozygote
MACSNP017031370998 chr7: 29523 PM1 Intergenic T C
homozygote
MACSNP017031371008 chr7: 29877 PM1 Intergenic T C
homozygote
MACSNP017031371033 chr7: 32143 PM1 Intergenic A G
homozygote

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