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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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178939 SNVs 1 of 17894 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP019070912476 chr19: 27729 LM1 Intergenic G A
homozygote
MACSNP019070912484 chr19: 28120 LM1 Intergenic A T
homozygote
MACSNP019070912501 chr19: 28452 LM1 Intergenic T A
homozygote
MACSNP019070912509 chr19: 28574 LM1 Intergenic T C
homozygote
MACSNP019070912522 chr19: 29470 LM1 Intergenic T A
homozygote
MACSNP019070912525 chr19: 29554 LM1 Intergenic G C
heterozygote
MACSNP019070912537 chr19: 29798 LM1 Intergenic T C
homozygote
MACSNP019070912540 chr19: 29858 LM1 Intergenic T G
homozygote
MACSNP019070912543 chr19: 29966 LM1 Intergenic T C
homozygote
MACSNP019070912549 chr19: 30045 LM1 Intergenic A G
homozygote

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