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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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417602 SNVs 1 of 41761 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP005036100678 chr8: 395649 JM1 ENSMMUG00000011105: Intron
 C T
homozygote
MACSNP005036100685 chr8: 395904 JM1 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP005036100698 chr8: 396171 JM1 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP005036100699 chr8: 396271 JM1 ENSMMUG00000011105: Intron
 G A
heterozygote
MACSNP005036100703 chr8: 396371 JM1 ENSMMUG00000011105: Intron
 T C
homozygote
MACSNP005036100710 chr8: 396590 JM1 ENSMMUG00000011105: Intron
 T G
homozygote
MACSNP005036100736 chr8: 397360 JM1 ENSMMUG00000011105: Intron
 T C
heterozygote
MACSNP005036100745 chr8: 397575 JM1 ENSMMUG00000011105: Intron
 A C
homozygote
MACSNP005036100755 chr8: 397976 JM1 ENSMMUG00000011105: Intron
 T A
homozygote
MACSNP005036100762 chr8: 398226 JM1 ENSMMUG00000011105: Intron
 G T
homozygote

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