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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
Show entries
706498 SNVs 1 of 70650 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010026079066 chr6: 17623 CE4 Intergenic C T
homozygote
MACSNP010026079071 chr6: 22910 CE4 Intergenic T C
heterozygote
MACSNP010026079100 chr6: 26867 CE4 Intergenic G C
homozygote
MACSNP010026079110 chr6: 28795 CE4 Intergenic A T
homozygote
MACSNP010026079127 chr6: 38929 CE4 Intergenic C T
homozygote
MACSNP010026079130 chr6: 39077 CE4 Intergenic T C
homozygote
MACSNP010026079135 chr6: 39552 CE4 Intergenic T A
homozygote
MACSNP010026079138 chr6: 39787 CE4 Intergenic C A
homozygote
MACSNP010026079145 chr6: 41754 CE4 Intergenic C A
homozygote
MACSNP010026079152 chr6: 43465 CE4 Intergenic T C
homozygote

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