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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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769955 SNVs 1 of 76996 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP015005515250 chr2: 35282 SM1 Intergenic T G
homozygote
MACSNP015005515267 chr2: 37271 SM1 Intergenic A T
homozygote
MACSNP015005515269 chr2: 37401 SM1 Intergenic T C
homozygote
MACSNP015005515270 chr2: 37608 SM1 Intergenic T C
homozygote
MACSNP015005515278 chr2: 38137 SM1 Intergenic T C
homozygote
MACSNP015005515291 chr2: 39585 SM1 Intergenic A G
homozygote
MACSNP015005515292 chr2: 39593 SM1 Intergenic G C
homozygote
MACSNP015005515307 chr2: 41067 SM1 Intergenic C T
homozygote
MACSNP015005515312 chr2: 41406 SM1 Intergenic G A
homozygote
MACSNP015005515317 chr2: 41971 SM1 Intergenic A G
homozygote

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