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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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485784 SNVs 1 of 48579 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016056871533 chr14: 3954 SM2 Intergenic A G
homozygote
MACSNP016056871538 chr14: 4174 SM2 Intergenic T C
homozygote
MACSNP016056871539 chr14: 4190 SM2 Intergenic G A
homozygote
MACSNP016056871548 chr14: 4610 SM2 Intergenic G T
homozygote
MACSNP016056871551 chr14: 4684 SM2 Intergenic A T
homozygote
MACSNP016056871557 chr14: 4889 SM2 Intergenic C T
homozygote
MACSNP016056871559 chr14: 4939 SM2 Intergenic T C
homozygote
MACSNP016056871563 chr14: 5042 SM2 Intergenic T C
homozygote
MACSNP016056871570 chr14: 5470 SM2 Intergenic C T
homozygote
MACSNP016056871572 chr14: 5523 SM2 Intergenic G A
homozygote

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