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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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239348 SNVs 1 of 23935 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011063857297 chr16: 997 CE5 Intergenic T C
homozygote
MACSNP011063857310 chr16: 1260 CE5 Intergenic G T
homozygote
MACSNP011063857320 chr16: 1616 CE5 Intergenic G A
heterozygote
MACSNP011063857350 chr16: 3151 CE5 Intergenic C T
homozygote
MACSNP011063857355 chr16: 3350 CE5 Intergenic C T
homozygote
MACSNP011063857356 chr16: 3357 CE5 Intergenic G A
homozygote
MACSNP011063857360 chr16: 3562 CE5 Intergenic C G
homozygote
MACSNP011063857366 chr16: 3735 CE5 Intergenic C T
homozygote
MACSNP011063857396 chr16: 5464 CE5 Intergenic A G
homozygote
MACSNP011063857400 chr16: 5667 CE5 Intergenic C T
homozygote

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