Filter SNVs Using Feature Selection

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314285 SNVs 1 of 31429 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007072229809 chr20: 375 CE1 Intergenic G A
homozygote
MACSNP007072229816 chr20: 1213 CE1 Intergenic C T
heterozygote
MACSNP007072229819 chr20: 1391 CE1 Intergenic T C
homozygote
MACSNP007072229827 chr20: 5304 CE1 ENSMMUG00000000586: Intron
A G
homozygote
MACSNP007072229835 chr20: 5667 CE1 ENSMMUG00000000586: Intron
A G
homozygote
MACSNP007072229838 chr20: 5710 CE1 ENSMMUG00000000586: Intron
C G
homozygote
MACSNP007072229840 chr20: 5806 CE1 ENSMMUG00000000586: Intron
C T
homozygote
MACSNP007072229886 chr20: 9236 CE1 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
G A
homozygote
MACSNP007072229893 chr20: 9635 CE1 ENSMMUG00000000586: CDS
ENSMMUG00000047475: 5'UTR
C T
homozygote
MACSNP007072229894 chr20: 9696 CE1 ENSMMUG00000000586: 5'UTR
ENSMMUG00000047475: 5'UTR
C T
homozygote