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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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907128 SNVs 1 of 90713 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017000000010 chr1: 9596 PM1 Intergenic C A
homozygote
MACSNP017000000024 chr1: 9909 PM1 Intergenic T C
homozygote
MACSNP017000000039 chr1: 10234 PM1 Intergenic C T
heterozygote
MACSNP017000000042 chr1: 10361 PM1 Intergenic G A
heterozygote
MACSNP017000000044 chr1: 10381 PM1 Intergenic G A
heterozygote
MACSNP017000000047 chr1: 10429 PM1 Intergenic T C
heterozygote
MACSNP017000000049 chr1: 10487 PM1 Intergenic T C
heterozygote
MACSNP017000000055 chr1: 10548 PM1 Intergenic G A
heterozygote
MACSNP017000000056 chr1: 10569 PM1 Intergenic C T
homozygote
MACSNP017000000061 chr1: 10631 PM1 Intergenic G A
heterozygote

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