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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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647442 SNVs 1 of 64745 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013026079065 chr6: 17502 TM2 Intergenic C T
homozygote
MACSNP013026079069 chr6: 22395 TM2 Intergenic C T
homozygote
MACSNP013026079075 chr6: 23346 TM2 Intergenic G A
homozygote
MACSNP013026079090 chr6: 25025 TM2 Intergenic G C
homozygote
MACSNP013026079091 chr6: 25120 TM2 Intergenic G C
heterozygote
MACSNP013026079100 chr6: 26867 TM2 Intergenic G C
homozygote
MACSNP013026079107 chr6: 28178 TM2 Intergenic C T
homozygote
MACSNP013026079127 chr6: 38929 TM2 Intergenic C T
homozygote
MACSNP013026079130 chr6: 39077 TM2 Intergenic T C
homozygote
MACSNP013026079138 chr6: 39787 TM2 Intergenic C A
homozygote

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