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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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234358 SNVs 1 of 23436 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013063857297 chr16: 997 TM2 Intergenic T C
homozygote
MACSNP013063857299 chr16: 1037 TM2 Intergenic T C
homozygote
MACSNP013063857304 chr16: 1176 TM2 Intergenic T C
homozygote
MACSNP013063857355 chr16: 3350 TM2 Intergenic C T
homozygote
MACSNP013063857357 chr16: 3378 TM2 Intergenic G A
homozygote
MACSNP013063857368 chr16: 3842 TM2 Intergenic G A
homozygote
MACSNP013063857377 chr16: 4326 TM2 Intergenic G A
homozygote
MACSNP013063857379 chr16: 4481 TM2 Intergenic T C
homozygote
MACSNP013063857383 chr16: 4753 TM2 Intergenic T C
homozygote
MACSNP013063857387 chr16: 4857 TM2 Intergenic A G
homozygote

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