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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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357207 SNVs 1 of 35721 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP018072229825 chr20: 5199 PM2 ENSMMUG00000000586: Intron
 T C
homozygote
MACSNP018072229828 chr20: 5341 PM2 ENSMMUG00000000586: Intron
 T C
homozygote
MACSNP018072229831 chr20: 5457 PM2 ENSMMUG00000000586: Intron
 T C
homozygote
MACSNP018072229851 chr20: 7148 PM2 ENSMMUG00000000586: Intron
 A G
homozygote
MACSNP018072229860 chr20: 7656 PM2 ENSMMUG00000000586: Intron
 A G
homozygote
MACSNP018072229889 chr20: 9422 PM2 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
 A C
homozygote
MACSNP018072229891 chr20: 9466 PM2 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
 A G
homozygote
MACSNP018072229893 chr20: 9635 PM2 ENSMMUG00000000586: CDS
ENSMMUG00000047475: 5'UTR
 C T
homozygote
MACSNP018072229894 chr20: 9696 PM2 ENSMMUG00000000586: 5'UTR
ENSMMUG00000047475: 5'UTR
 C T
homozygote
MACSNP018072229900 chr20: 9880 PM2 ENSMMUG00000047475: 5'UTR
 A G
heterozygote

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