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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
162869 SNVs 1 of 16287 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002068733183 chr18: 310 CR2 Intergenic A G
homozygote
MACSNP002068733223 chr18: 1150 CR2 Intergenic C T
homozygote
MACSNP002068733244 chr18: 2051 CR2 Intergenic T C
homozygote
MACSNP002068733268 chr18: 2676 CR2 Intergenic T G
homozygote
MACSNP002068733293 chr18: 3450 CR2 Intergenic C T
homozygote
MACSNP002068733297 chr18: 3555 CR2 Intergenic C T
homozygote
MACSNP002068733331 chr18: 4442 CR2 Intergenic T C
homozygote
MACSNP002068733332 chr18: 4475 CR2 Intergenic C T
homozygote
MACSNP002068733372 chr18: 5560 CR2 Intergenic G T
homozygote
MACSNP002068733403 chr18: 6380 CR2 Intergenic G T
homozygote

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