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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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295879 SNVs 1 of 29588 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP019068733181 chr18: 276 LM1 Intergenic A T
homozygote
MACSNP019068733183 chr18: 310 LM1 Intergenic A G
homozygote
MACSNP019068733185 chr18: 387 LM1 Intergenic A G
homozygote
MACSNP019068733209 chr18: 757 LM1 Intergenic C T
homozygote
MACSNP019068733217 chr18: 931 LM1 Intergenic C T
homozygote
MACSNP019068733221 chr18: 1125 LM1 Intergenic A T
homozygote
MACSNP019068733232 chr18: 1545 LM1 Intergenic C T
homozygote
MACSNP019068733244 chr18: 2051 LM1 Intergenic T C
homozygote
MACSNP019068733247 chr18: 2209 LM1 Intergenic C G
homozygote
MACSNP019068733248 chr18: 2220 LM1 Intergenic A G
homozygote

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