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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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314511 SNVs 1 of 31452 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP015068733178 chr18: 182 SM1 Intergenic A G
homozygote
MACSNP015068733183 chr18: 310 SM1 Intergenic A G
homozygote
MACSNP015068733187 chr18: 497 SM1 Intergenic A G
homozygote
MACSNP015068733193 chr18: 569 SM1 Intergenic C G
homozygote
MACSNP015068733194 chr18: 569 SM1 Intergenic C G
homozygote
MACSNP015068733217 chr18: 931 SM1 Intergenic C T
homozygote
MACSNP015068733242 chr18: 1935 SM1 Intergenic A G
homozygote
MACSNP015068733244 chr18: 2051 SM1 Intergenic T C
homozygote
MACSNP015068733248 chr18: 2220 SM1 Intergenic A G
homozygote
MACSNP015068733281 chr18: 2908 SM1 Intergenic A C
homozygote

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