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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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439685 SNVs 1 of 43969 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020072229826 chr20: 5292 BM1 ENSMMUG00000000586: Intron
 C T
homozygote
MACSNP020072229834 chr20: 5641 BM1 ENSMMUG00000000586: Intron
 T C
homozygote
MACSNP020072229840 chr20: 5806 BM1 ENSMMUG00000000586: Intron
 C T
homozygote
MACSNP020072229872 chr20: 8659 BM1 ENSMMUG00000000586: Intron
 C G
heterozygote
MACSNP020072229874 chr20: 8724 BM1 ENSMMUG00000000586: Intron
 A G
heterozygote
MACSNP020072229875 chr20: 8734 BM1 ENSMMUG00000000586: Intron
 T C
heterozygote
MACSNP020072229877 chr20: 8763 BM1 ENSMMUG00000000586: Intron
 A T
heterozygote
MACSNP020072229888 chr20: 9408 BM1 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
 G A
homozygote
MACSNP020072229890 chr20: 9450 BM1 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
 G C
homozygote
MACSNP020072229893 chr20: 9635 BM1 ENSMMUG00000000586: CDS
ENSMMUG00000047475: 5'UTR
 C T
homozygote

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