Filter SNVs Using Feature Selection

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361811 SNVs 1 of 36182 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017072229825 chr20: 5199 PM1 ENSMMUG00000000586: Intron
T C
homozygote
MACSNP017072229831 chr20: 5457 PM1 ENSMMUG00000000586: Intron
T C
homozygote
MACSNP017072229840 chr20: 5806 PM1 ENSMMUG00000000586: Intron
C T
homozygote
MACSNP017072229842 chr20: 5897 PM1 ENSMMUG00000000586: Intron
C G
homozygote
MACSNP017072229847 chr20: 6157 PM1 ENSMMUG00000000586: Intron
A G
heterozygote
MACSNP017072229857 chr20: 7496 PM1 ENSMMUG00000000586: Intron
C T
heterozygote
MACSNP017072229864 chr20: 8358 PM1 ENSMMUG00000000586: Intron
C T
homozygote
MACSNP017072229876 chr20: 8736 PM1 ENSMMUG00000000586: Intron
A C
heterozygote
MACSNP017072229878 chr20: 8790 PM1 ENSMMUG00000000586: Intron
T C
heterozygote
MACSNP017072229879 chr20: 8816 PM1 ENSMMUG00000000586: Intron
C A
heterozygote