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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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269004 SNVs 1 of 26901 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002056871533 chr14: 3954 CR2 Intergenic A G
homozygote
MACSNP002056871536 chr14: 4069 CR2 Intergenic T C
homozygote
MACSNP002056871556 chr14: 4873 CR2 Intergenic G A
heterozygote
MACSNP002056871580 chr14: 5697 CR2 Intergenic A T
homozygote
MACSNP002056871581 chr14: 5726 CR2 Intergenic T C
homozygote
MACSNP002056871597 chr14: 6242 CR2 Intergenic T C
homozygote
MACSNP002056871642 chr14: 8072 CR2 Intergenic G A
heterozygote
MACSNP002056871649 chr14: 8378 CR2 ENSMMUG00000011502: Intron
 C G
homozygote
MACSNP002056871666 chr14: 9134 CR2 ENSMMUG00000011502: Intron
ENSMMUG00000011502: CDS
 C T
heterozygote
MACSNP002056871675 chr14: 9704 CR2 ENSMMUG00000011502: Intron
 G A
heterozygote

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