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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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618478 SNVs 1 of 61848 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016031370888 chr7: 18903 SM2 Intergenic C T
heterozygote
MACSNP016031370926 chr7: 25653 SM2 Intergenic G A
homozygote
MACSNP016031370943 chr7: 26836 SM2 Intergenic A G
homozygote
MACSNP016031370958 chr7: 27846 SM2 Intergenic A C
homozygote
MACSNP016031370961 chr7: 28037 SM2 Intergenic C G
homozygote
MACSNP016031370975 chr7: 28771 SM2 Intergenic T C
heterozygote
MACSNP016031370988 chr7: 29280 SM2 Intergenic G A
homozygote
MACSNP016031370992 chr7: 29412 SM2 Intergenic C T
homozygote
MACSNP016031370994 chr7: 29425 SM2 Intergenic T A
heterozygote
MACSNP016031371033 chr7: 32143 SM2 Intergenic A G
homozygote

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