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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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702109 SNVs 1 of 70211 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020040365691 chr9: 2565 BM1 Intergenic G A
homozygote
MACSNP020040365701 chr9: 2868 BM1 Intergenic C A
homozygote
MACSNP020040365708 chr9: 3219 BM1 Intergenic T G
homozygote
MACSNP020040365788 chr9: 14318 BM1 Intergenic G A
homozygote
MACSNP020040365789 chr9: 14327 BM1 Intergenic A G
homozygote
MACSNP020040365791 chr9: 14375 BM1 Intergenic G A
homozygote
MACSNP020040365802 chr9: 14593 BM1 Intergenic G C
homozygote
MACSNP020040365803 chr9: 14629 BM1 Intergenic G A
homozygote
MACSNP020040365821 chr9: 15119 BM1 Intergenic G A
homozygote
MACSNP020040365832 chr9: 15362 BM1 Intergenic C A
homozygote

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