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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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506526 SNVs 1 of 50653 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001031370838 chr7: 8961 CR1 Intergenic T C
heterozygote
MACSNP001031370843 chr7: 10468 CR1 Intergenic A G
homozygote
MACSNP001031370848 chr7: 10577 CR1 Intergenic A G
homozygote
MACSNP001031370849 chr7: 10604 CR1 Intergenic C A
homozygote
MACSNP001031370882 chr7: 18841 CR1 Intergenic C A
heterozygote
MACSNP001031370884 chr7: 18870 CR1 Intergenic A G
heterozygote
MACSNP001031370887 chr7: 18897 CR1 Intergenic C T
heterozygote
MACSNP001031370889 chr7: 18929 CR1 Intergenic C T
heterozygote
MACSNP001031370890 chr7: 18938 CR1 Intergenic C T
heterozygote
MACSNP001031370893 chr7: 18972 CR1 Intergenic A G
heterozygote

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