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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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315123 SNVs 1 of 31513 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP014072229830 chr20: 5371 AM1 ENSMMUG00000000586: Intron
 T C
heterozygote
MACSNP014072229832 chr20: 5475 AM1 ENSMMUG00000000586: Intron
 T C
homozygote
MACSNP014072229871 chr20: 8642 AM1 ENSMMUG00000000586: Intron
 G T
heterozygote
MACSNP014072229886 chr20: 9236 AM1 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
 G A
homozygote
MACSNP014072229903 chr20: 9915 AM1 ENSMMUG00000047475: 5'UTR
 A G
homozygote
MACSNP014072229939 chr20: 11042 AM1 ENSMMUG00000047475: Intron
 C T
heterozygote
MACSNP014072229949 chr20: 11284 AM1 ENSMMUG00000047475: Intron
 A G
homozygote
MACSNP014072230002 chr20: 13530 AM1 ENSMMUG00000047475: 3'UTR
 A G
homozygote
MACSNP014072230008 chr20: 13713 AM1 Intergenic C T
heterozygote
MACSNP014072230009 chr20: 13779 AM1 Intergenic A G
heterozygote

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