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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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130046 SNVs 1 of 13005 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP004070912549 chr19: 30045 TW1 Intergenic A G
homozygote
MACSNP004070912555 chr19: 30139 TW1 Intergenic T C
homozygote
MACSNP004070912607 chr19: 33526 TW1 Intergenic A G
homozygote
MACSNP004070912616 chr19: 33744 TW1 Intergenic C T
homozygote
MACSNP004070912617 chr19: 33806 TW1 Intergenic A G
homozygote
MACSNP004070912620 chr19: 33879 TW1 Intergenic T A
homozygote
MACSNP004070912621 chr19: 33888 TW1 Intergenic C T
homozygote
MACSNP004070912649 chr19: 34683 TW1 Intergenic T C
homozygote
MACSNP004070912684 chr19: 35201 TW1 Intergenic T C
homozygote
MACSNP004070912696 chr19: 35289 TW1 Intergenic T C
homozygote

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