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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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442440 SNVs 1 of 44244 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006031370886 chr7: 18884 JM2 Intergenic G A
heterozygote
MACSNP006031370889 chr7: 18929 JM2 Intergenic C T
heterozygote
MACSNP006031370890 chr7: 18938 JM2 Intergenic C T
heterozygote
MACSNP006031370894 chr7: 18980 JM2 Intergenic G A
heterozygote
MACSNP006031370897 chr7: 19012 JM2 Intergenic A G
heterozygote
MACSNP006031370898 chr7: 19018 JM2 Intergenic T C
heterozygote
MACSNP006031370937 chr7: 25981 JM2 Intergenic T C
heterozygote
MACSNP006031370973 chr7: 28690 JM2 Intergenic G A
heterozygote
MACSNP006031370979 chr7: 29019 JM2 Intergenic G A
heterozygote
MACSNP006031370992 chr7: 29412 JM2 Intergenic C T
homozygote

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