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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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191843 SNVs 1 of 19185 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP015070912470 chr19: 27078 SM1 Intergenic G T
heterozygote
MACSNP015070912471 chr19: 27548 SM1 Intergenic T A
homozygote
MACSNP015070912476 chr19: 27729 SM1 Intergenic G A
homozygote
MACSNP015070912487 chr19: 28151 SM1 Intergenic G C
homozygote
MACSNP015070912505 chr19: 28542 SM1 Intergenic C G
homozygote
MACSNP015070912514 chr19: 28781 SM1 Intergenic A G
homozygote
MACSNP015070912517 chr19: 29398 SM1 Intergenic G A
homozygote
MACSNP015070912518 chr19: 29409 SM1 Intergenic G C
homozygote
MACSNP015070912527 chr19: 29594 SM1 Intergenic A G
homozygote
MACSNP015070912536 chr19: 29797 SM1 Intergenic T C
homozygote

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