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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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408077 SNVs 1 of 40808 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013060569918 chr15: 37741 TM2 Intergenic C T
homozygote
MACSNP013060569937 chr15: 39621 TM2 Intergenic C T
homozygote
MACSNP013060569938 chr15: 39640 TM2 Intergenic C T
homozygote
MACSNP013060569981 chr15: 45570 TM2 Intergenic A G
homozygote
MACSNP013060569994 chr15: 47698 TM2 Intergenic G T
homozygote
MACSNP013060570004 chr15: 48578 TM2 Intergenic A G
homozygote
MACSNP013060570011 chr15: 48799 TM2 Intergenic A C
homozygote
MACSNP013060570055 chr15: 49671 TM2 Intergenic T C
homozygote
MACSNP013060570058 chr15: 49711 TM2 Intergenic C A
homozygote
MACSNP013060570230 chr15: 60671 TM2 Intergenic T C
homozygote

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