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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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315075 SNVs 1 of 31508 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP004053619597 chr13: 7065 TW1 Intergenic G A
heterozygote
MACSNP004053619616 chr13: 8734 TW1 Intergenic G T
heterozygote
MACSNP004053619694 chr13: 17859 TW1 Intergenic A G
heterozygote
MACSNP004053619708 chr13: 19650 TW1 Intergenic A G
heterozygote
MACSNP004053619711 chr13: 19946 TW1 Intergenic C T
heterozygote
MACSNP004053619714 chr13: 19993 TW1 Intergenic A G
heterozygote
MACSNP004053619747 chr13: 20989 TW1 Intergenic G A
heterozygote
MACSNP004053619748 chr13: 20995 TW1 Intergenic G C
heterozygote
MACSNP004053619750 chr13: 21037 TW1 Intergenic T C
homozygote
MACSNP004053619831 chr13: 27701 TW1 Intergenic A G
heterozygote

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