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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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182627 SNVs 1 of 18263 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP012070912489 chr19: 28199 TM1 Intergenic A G
homozygote
MACSNP012070912496 chr19: 28345 TM1 Intergenic T C
homozygote
MACSNP012070912515 chr19: 29325 TM1 Intergenic G A
homozygote
MACSNP012070912518 chr19: 29409 TM1 Intergenic G C
homozygote
MACSNP012070912522 chr19: 29470 TM1 Intergenic T A
homozygote
MACSNP012070912530 chr19: 29618 TM1 Intergenic T C
homozygote
MACSNP012070912549 chr19: 30045 TM1 Intergenic A G
homozygote
MACSNP012070912555 chr19: 30139 TM1 Intergenic T C
homozygote
MACSNP012070912570 chr19: 30495 TM1 Intergenic A T
homozygote
MACSNP012070912572 chr19: 30670 TM1 Intergenic A G
homozygote

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