Filter SNVs Using Feature Selection

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303925 SNVs 1 of 30393 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011072229813 chr20: 840 CE5 Intergenic G A
heterozygote
MACSNP011072229819 chr20: 1391 CE5 Intergenic T C
homozygote
MACSNP011072229827 chr20: 5304 CE5 ENSMMUG00000000586: Intron
A G
homozygote
MACSNP011072229835 chr20: 5667 CE5 ENSMMUG00000000586: Intron
A G
homozygote
MACSNP011072229838 chr20: 5710 CE5 ENSMMUG00000000586: Intron
C G
homozygote
MACSNP011072229840 chr20: 5806 CE5 ENSMMUG00000000586: Intron
C T
homozygote
MACSNP011072229869 chr20: 8567 CE5 ENSMMUG00000000586: Intron
A C
heterozygote
MACSNP011072229886 chr20: 9236 CE5 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
G A
homozygote
MACSNP011072229931 chr20: 10864 CE5 ENSMMUG00000047475: Intron
G C
homozygote
MACSNP011072229932 chr20: 10886 CE5 ENSMMUG00000047475: Intron
G A
homozygote