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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
318112 SNVs 1 of 31812 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP012072229807 chr20: 175 TM1 Intergenic C T
homozygote
MACSNP012072229815 chr20: 1177 TM1 Intergenic G C
homozygote
MACSNP012072229832 chr20: 5475 TM1 ENSMMUG00000000586: Intron
 T C
homozygote
MACSNP012072229840 chr20: 5806 TM1 ENSMMUG00000000586: Intron
 C T
homozygote
MACSNP012072229852 chr20: 7174 TM1 ENSMMUG00000000586: Intron
 A C
homozygote
MACSNP012072229867 chr20: 8449 TM1 ENSMMUG00000000586: Intron
 C G
homozygote
MACSNP012072229893 chr20: 9635 TM1 ENSMMUG00000000586: CDS
ENSMMUG00000047475: 5'UTR
 C T
homozygote
MACSNP012072229908 chr20: 9999 TM1 ENSMMUG00000047475: 5'UTR
 T G
homozygote
MACSNP012072229940 chr20: 11048 TM1 ENSMMUG00000047475: Intron
 T C
homozygote
MACSNP012072229949 chr20: 11284 TM1 ENSMMUG00000047475: Intron
 A G
homozygote

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