Filter SNVs Using Feature Selection

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685268 SNVs 1 of 68527 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP018036100654 chr8: 234711 PM2 ENSMMUG00000020598: Intron
A G
heterozygote
MACSNP018036100666 chr8: 395461 PM2 ENSMMUG00000011105: Intron
T C
heterozygote
MACSNP018036100667 chr8: 395472 PM2 ENSMMUG00000011105: Intron
T C
heterozygote
MACSNP018036100670 chr8: 395511 PM2 ENSMMUG00000011105: Intron
T C
homozygote
MACSNP018036100681 chr8: 395714 PM2 ENSMMUG00000011105: Intron
C T
heterozygote
MACSNP018036100682 chr8: 395770 PM2 ENSMMUG00000011105: Intron
T C
heterozygote
MACSNP018036100684 chr8: 395865 PM2 ENSMMUG00000011105: Intron
T A
heterozygote
MACSNP018036100685 chr8: 395904 PM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP018036100690 chr8: 396074 PM2 ENSMMUG00000011105: Intron
G T
heterozygote
MACSNP018036100698 chr8: 396171 PM2 ENSMMUG00000011105: Intron
A G
homozygote