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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
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218892 SNVs 1 of 21890 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP005072229845 chr20: 6063 JM1 ENSMMUG00000000586: Intron
 A T
homozygote
MACSNP005072229873 chr20: 8700 JM1 ENSMMUG00000000586: Intron
 C G
homozygote
MACSNP005072229887 chr20: 9376 JM1 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
 G T
heterozygote
MACSNP005072229896 chr20: 9730 JM1 ENSMMUG00000000586: 5'UTR
ENSMMUG00000047475: 5'UTR
 C A
heterozygote
MACSNP005072229904 chr20: 9919 JM1 ENSMMUG00000047475: 5'UTR
 C G
heterozygote
MACSNP005072229915 chr20: 10349 JM1 ENSMMUG00000047475: Intron
 A C
homozygote
MACSNP005072229918 chr20: 10450 JM1 ENSMMUG00000047475: Intron
 C A
homozygote
MACSNP005072229920 chr20: 10514 JM1 ENSMMUG00000047475: Intron
 A G
homozygote
MACSNP005072229931 chr20: 10864 JM1 ENSMMUG00000047475: Intron
 G C
homozygote
MACSNP005072229940 chr20: 11048 JM1 ENSMMUG00000047475: Intron
 T C
homozygote

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