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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
373636 SNVs 1 of 37364 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002026079107 chr6: 28178 CR2 Intergenic C T
homozygote
MACSNP002026079120 chr6: 31233 CR2 Intergenic T G
homozygote
MACSNP002026079149 chr6: 42774 CR2 Intergenic A C
homozygote
MACSNP002026079161 chr6: 44532 CR2 Intergenic G A
homozygote
MACSNP002026079178 chr6: 46945 CR2 Intergenic G A
homozygote
MACSNP002026079251 chr6: 54063 CR2 Intergenic G A
homozygote
MACSNP002026079256 chr6: 54520 CR2 Intergenic G C
homozygote
MACSNP002026079263 chr6: 55275 CR2 Intergenic G C
homozygote
MACSNP002026079275 chr6: 55917 CR2 Intergenic T G
heterozygote
MACSNP002026079276 chr6: 55990 CR2 Intergenic A G
homozygote

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