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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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298988 SNVs 1 of 29899 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP009072229835 chr20: 5667 CE3 ENSMMUG00000000586: Intron
 A G
homozygote
MACSNP009072229838 chr20: 5710 CE3 ENSMMUG00000000586: Intron
 C G
homozygote
MACSNP009072229840 chr20: 5806 CE3 ENSMMUG00000000586: Intron
 C T
homozygote
MACSNP009072229847 chr20: 6157 CE3 ENSMMUG00000000586: Intron
 A G
heterozygote
MACSNP009072229886 chr20: 9236 CE3 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
 G A
homozygote
MACSNP009072229915 chr20: 10349 CE3 ENSMMUG00000047475: Intron
 A C
homozygote
MACSNP009072229916 chr20: 10364 CE3 ENSMMUG00000047475: Intron
 G A
heterozygote
MACSNP009072229931 chr20: 10864 CE3 ENSMMUG00000047475: Intron
 G C
homozygote
MACSNP009072229932 chr20: 10886 CE3 ENSMMUG00000047475: Intron
 G A
homozygote
MACSNP009072229933 chr20: 10903 CE3 ENSMMUG00000047475: Intron
 G A
homozygote

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