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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
332900 SNVs 1 of 33290 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP015072229807 chr20: 175 SM1 Intergenic C T
homozygote
MACSNP015072229810 chr20: 513 SM1 Intergenic A G
heterozygote
MACSNP015072229814 chr20: 986 SM1 Intergenic A T
homozygote
MACSNP015072229817 chr20: 1232 SM1 Intergenic T G
homozygote
MACSNP015072229818 chr20: 1253 SM1 Intergenic A G
homozygote
MACSNP015072229830 chr20: 5371 SM1 ENSMMUG00000000586: Intron
 T C
heterozygote
MACSNP015072229832 chr20: 5475 SM1 ENSMMUG00000000586: Intron
 T C
heterozygote
MACSNP015072229840 chr20: 5806 SM1 ENSMMUG00000000586: Intron
 C T
homozygote
MACSNP015072229852 chr20: 7174 SM1 ENSMMUG00000000586: Intron
 A C
heterozygote
MACSNP015072229858 chr20: 7535 SM1 ENSMMUG00000000586: Intron
 G A
heterozygote

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