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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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670794 SNVs 1 of 67080 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013000000037 chr1: 10194 TM2 Intergenic T C
homozygote
MACSNP013000000064 chr1: 10671 TM2 Intergenic G C
homozygote
MACSNP013000000070 chr1: 10885 TM2 Intergenic T C
homozygote
MACSNP013000000076 chr1: 10945 TM2 Intergenic G A
homozygote
MACSNP013000000077 chr1: 10979 TM2 Intergenic G C
homozygote
MACSNP013000000083 chr1: 11109 TM2 Intergenic T C
homozygote
MACSNP013000000093 chr1: 11405 TM2 Intergenic A G
homozygote
MACSNP013000000099 chr1: 11533 TM2 Intergenic A G
homozygote
MACSNP013000000101 chr1: 11609 TM2 Intergenic A G
homozygote
MACSNP013000000104 chr1: 11664 TM2 Intergenic C T
homozygote

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