Filter SNVs Using Feature Selection

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295557 SNVs 1 of 29556 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016072229808 chr20: 325 SM2 Intergenic G A
heterozygote
MACSNP016072229821 chr20: 4827 SM2 ENSMMUG00000000586: Intron
T A
heterozygote
MACSNP016072229824 chr20: 5161 SM2 ENSMMUG00000000586: Intron
G T
heterozygote
MACSNP016072229830 chr20: 5371 SM2 ENSMMUG00000000586: Intron
T C
heterozygote
MACSNP016072229832 chr20: 5475 SM2 ENSMMUG00000000586: Intron
T C
heterozygote
MACSNP016072229840 chr20: 5806 SM2 ENSMMUG00000000586: Intron
C T
homozygote
MACSNP016072229848 chr20: 6160 SM2 ENSMMUG00000000586: Intron
G T
heterozygote
MACSNP016072229852 chr20: 7174 SM2 ENSMMUG00000000586: Intron
A C
heterozygote
MACSNP016072229859 chr20: 7582 SM2 ENSMMUG00000000586: Intron
C G
heterozygote
MACSNP016072229861 chr20: 7737 SM2 ENSMMUG00000000586: Intron
G T
heterozygote