Filter SNVs Using Feature Selection

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244867 SNVs 1 of 24487 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001072229809 chr20: 375 CR1 Intergenic G A
heterozygote
MACSNP001072229837 chr20: 5681 CR1 ENSMMUG00000000586: Intron
G A
heterozygote
MACSNP001072229845 chr20: 6063 CR1 ENSMMUG00000000586: Intron
A T
homozygote
MACSNP001072229873 chr20: 8700 CR1 ENSMMUG00000000586: Intron
C G
homozygote
MACSNP001072229885 chr20: 9190 CR1 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
G A
heterozygote
MACSNP001072229915 chr20: 10349 CR1 ENSMMUG00000047475: Intron
A C
homozygote
MACSNP001072229918 chr20: 10450 CR1 ENSMMUG00000047475: Intron
C A
homozygote
MACSNP001072229920 chr20: 10514 CR1 ENSMMUG00000047475: Intron
A G
homozygote
MACSNP001072229931 chr20: 10864 CR1 ENSMMUG00000047475: Intron
G C
heterozygote
MACSNP001072229932 chr20: 10886 CR1 ENSMMUG00000047475: Intron
G A
heterozygote