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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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476136 SNVs 1 of 47614 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP015053619570 chr13: 1350 SM1 Intergenic C T
heterozygote
MACSNP015053619572 chr13: 1438 SM1 Intergenic G C
heterozygote
MACSNP015053619576 chr13: 1609 SM1 Intergenic T C
heterozygote
MACSNP015053619581 chr13: 1702 SM1 Intergenic G T
heterozygote
MACSNP015053619699 chr13: 19120 SM1 Intergenic C T
heterozygote
MACSNP015053619700 chr13: 19164 SM1 Intergenic C T
heterozygote
MACSNP015053619716 chr13: 20091 SM1 Intergenic A G
heterozygote
MACSNP015053619718 chr13: 20116 SM1 Intergenic C T
heterozygote
MACSNP015053619720 chr13: 20192 SM1 Intergenic A G
heterozygote
MACSNP015053619727 chr13: 20504 SM1 Intergenic G A
heterozygote

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