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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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238855 SNVs 1 of 23886 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020070912476 chr19: 27729 BM1 Intergenic G A
homozygote
MACSNP020070912477 chr19: 27833 BM1 Intergenic C A
homozygote
MACSNP020070912496 chr19: 28345 BM1 Intergenic T C
homozygote
MACSNP020070912498 chr19: 28413 BM1 Intergenic G A
homozygote
MACSNP020070912507 chr19: 28556 BM1 Intergenic C G
homozygote
MACSNP020070912519 chr19: 29419 BM1 Intergenic A C
homozygote
MACSNP020070912521 chr19: 29461 BM1 Intergenic T C
homozygote
MACSNP020070912522 chr19: 29470 BM1 Intergenic T A
homozygote
MACSNP020070912524 chr19: 29520 BM1 Intergenic A G
homozygote
MACSNP020070912529 chr19: 29617 BM1 Intergenic A G
homozygote

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