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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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484063 SNVs 1 of 48407 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006005515270 chr2: 37608 JM2 Intergenic T C
homozygote
MACSNP006005515274 chr2: 37948 JM2 Intergenic T C
heterozygote
MACSNP006005515275 chr2: 37977 JM2 Intergenic T A
homozygote
MACSNP006005515279 chr2: 38356 JM2 Intergenic C A
homozygote
MACSNP006005515284 chr2: 38796 JM2 Intergenic A G
homozygote
MACSNP006005515286 chr2: 38863 JM2 Intergenic C T
homozygote
MACSNP006005515291 chr2: 39585 JM2 Intergenic A G
homozygote
MACSNP006005515292 chr2: 39593 JM2 Intergenic G C
homozygote
MACSNP006005515321 chr2: 42083 JM2 Intergenic T C
homozygote
MACSNP006005515322 chr2: 42095 JM2 Intergenic C T
heterozygote

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