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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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684595 SNVs 1 of 68460 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017036100652 chr8: 234621 PM1 ENSMMUG00000020598: Intron
 A G
heterozygote
MACSNP017036100653 chr8: 234643 PM1 ENSMMUG00000020598: Intron
 C G
heterozygote
MACSNP017036100654 chr8: 234711 PM1 ENSMMUG00000020598: Intron
 A G
heterozygote
MACSNP017036100662 chr8: 395413 PM1 ENSMMUG00000011105: Intron
 G A
homozygote
MACSNP017036100665 chr8: 395455 PM1 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP017036100670 chr8: 395511 PM1 ENSMMUG00000011105: Intron
 T C
homozygote
MACSNP017036100685 chr8: 395904 PM1 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP017036100698 chr8: 396171 PM1 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP017036100703 chr8: 396371 PM1 ENSMMUG00000011105: Intron
 T C
homozygote
MACSNP017036100705 chr8: 396471 PM1 ENSMMUG00000011105: Intron
 C T
homozygote

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