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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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831594 SNVs 1 of 83160 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP020036100647 chr8: 234126 BM1 ENSMMUG00000020598: Intron
 C A
heterozygote
MACSNP020036100656 chr8: 234818 BM1 ENSMMUG00000020598: Intron
 T C
homozygote
MACSNP020036100660 chr8: 395395 BM1 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP020036100661 chr8: 395412 BM1 ENSMMUG00000011105: Intron
 C T
homozygote
MACSNP020036100664 chr8: 395450 BM1 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP020036100668 chr8: 395475 BM1 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP020036100673 chr8: 395585 BM1 ENSMMUG00000011105: Intron
 G A
homozygote
MACSNP020036100679 chr8: 395678 BM1 ENSMMUG00000011105: Intron
 T G
homozygote
MACSNP020036100683 chr8: 395807 BM1 ENSMMUG00000011105: Intron
 G A
homozygote
MACSNP020036100685 chr8: 395904 BM1 ENSMMUG00000011105: Intron
 A G
homozygote

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