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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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672084 SNVs 1 of 67209 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP012031370837 chr7: 8917 TM1 Intergenic C T
homozygote
MACSNP012031370847 chr7: 10571 TM1 Intergenic G A
homozygote
MACSNP012031370945 chr7: 27051 TM1 Intergenic G T
homozygote
MACSNP012031370987 chr7: 29238 TM1 Intergenic C G
homozygote
MACSNP012031370992 chr7: 29412 TM1 Intergenic C T
homozygote
MACSNP012031370995 chr7: 29444 TM1 Intergenic G C
homozygote
MACSNP012031370998 chr7: 29523 TM1 Intergenic T C
homozygote
MACSNP012031371012 chr7: 30540 TM1 Intergenic A G
homozygote
MACSNP012031371033 chr7: 32143 TM1 Intergenic A G
homozygote
MACSNP012031371049 chr7: 33584 TM1 Intergenic T C
heterozygote

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