Filter SNVs Using Feature Selection

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415983 SNVs 1 of 41599 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011050510057 chr12: 38443 CE5 ENSMMUG00000009617: Intron
C G
homozygote
MACSNP011050510067 chr12: 39590 CE5 Intergenic G A
homozygote
MACSNP011050510070 chr12: 40345 CE5 Intergenic G A
heterozygote
MACSNP011050510072 chr12: 40601 CE5 Intergenic T C
homozygote
MACSNP011050510074 chr12: 40777 CE5 Intergenic C T
heterozygote
MACSNP011050510084 chr12: 46617 CE5 Intergenic C T
homozygote
MACSNP011050510085 chr12: 46997 CE5 Intergenic C T
heterozygote
MACSNP011050510100 chr12: 48146 CE5 Intergenic A C
heterozygote
MACSNP011050510104 chr12: 48427 CE5 Intergenic T G
homozygote
MACSNP011050510107 chr12: 48880 CE5 Intergenic A G
heterozygote