Filter SNVs Using Feature Selection

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315971 SNVs 1 of 31598 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP008072229819 chr20: 1391 CE2 Intergenic T C
homozygote
MACSNP008072229823 chr20: 4858 CE2 ENSMMUG00000000586: Intron
C G
heterozygote
MACSNP008072229827 chr20: 5304 CE2 ENSMMUG00000000586: Intron
A G
homozygote
MACSNP008072229835 chr20: 5667 CE2 ENSMMUG00000000586: Intron
A G
homozygote
MACSNP008072229855 chr20: 7405 CE2 ENSMMUG00000000586: CDS
C G
heterozygote
MACSNP008072229856 chr20: 7422 CE2 ENSMMUG00000000586: CDS
C A
heterozygote
MACSNP008072229863 chr20: 8052 CE2 ENSMMUG00000000586: Intron
C G
homozygote
MACSNP008072229886 chr20: 9236 CE2 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
G A
homozygote
MACSNP008072229894 chr20: 9696 CE2 ENSMMUG00000000586: 5'UTR
ENSMMUG00000047475: 5'UTR
C T
homozygote
MACSNP008072229915 chr20: 10349 CE2 ENSMMUG00000047475: Intron
A C
homozygote