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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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690687 SNVs 1 of 69069 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP019015522763 chr4: 17469 LM1 Intergenic G A
homozygote
MACSNP019015522793 chr4: 18481 LM1 Intergenic A G
homozygote
MACSNP019015522794 chr4: 18489 LM1 Intergenic T C
homozygote
MACSNP019015522795 chr4: 18529 LM1 Intergenic T C
homozygote
MACSNP019015522810 chr4: 19257 LM1 Intergenic T A
homozygote
MACSNP019015522829 chr4: 19918 LM1 Intergenic T C
homozygote
MACSNP019015522837 chr4: 20172 LM1 Intergenic C T
homozygote
MACSNP019015522838 chr4: 20180 LM1 Intergenic T A
homozygote
MACSNP019015522839 chr4: 20204 LM1 Intergenic A C
homozygote
MACSNP019015522840 chr4: 20262 LM1 Intergenic C T
homozygote

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