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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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469597 SNVs 1 of 46960 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006015522751 chr4: 16897 JM2 Intergenic T C
homozygote
MACSNP006015522752 chr4: 16920 JM2 Intergenic C T
homozygote
MACSNP006015522759 chr4: 17308 JM2 Intergenic T C
homozygote
MACSNP006015522763 chr4: 17469 JM2 Intergenic G A
homozygote
MACSNP006015522765 chr4: 17509 JM2 Intergenic G A
homozygote
MACSNP006015522768 chr4: 17609 JM2 Intergenic G A
homozygote
MACSNP006015522770 chr4: 17755 JM2 Intergenic C T
homozygote
MACSNP006015522772 chr4: 17833 JM2 Intergenic T A
homozygote
MACSNP006015522777 chr4: 17952 JM2 Intergenic G A
homozygote
MACSNP006015522780 chr4: 17990 JM2 Intergenic T C
homozygote

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