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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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513856 SNVs 1 of 51386 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP019056871526 chr14: 3756 LM1 Intergenic A G
homozygote
MACSNP019056871533 chr14: 3954 LM1 Intergenic A G
homozygote
MACSNP019056871537 chr14: 4077 LM1 Intergenic C G
homozygote
MACSNP019056871539 chr14: 4190 LM1 Intergenic G A
homozygote
MACSNP019056871544 chr14: 4478 LM1 Intergenic C T
homozygote
MACSNP019056871551 chr14: 4684 LM1 Intergenic A T
homozygote
MACSNP019056871559 chr14: 4939 LM1 Intergenic T C
homozygote
MACSNP019056871560 chr14: 4950 LM1 Intergenic G A
homozygote
MACSNP019056871563 chr14: 5042 LM1 Intergenic T C
homozygote
MACSNP019056871565 chr14: 5124 LM1 Intergenic G A
homozygote

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