Filter SNVs Using Feature Selection

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411204 SNVs 1 of 41121 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP009050510057 chr12: 38443 CE3 ENSMMUG00000009617: Intron
C G
homozygote
MACSNP009050510067 chr12: 39590 CE3 Intergenic G A
homozygote
MACSNP009050510072 chr12: 40601 CE3 Intergenic T C
homozygote
MACSNP009050510084 chr12: 46617 CE3 Intergenic C T
homozygote
MACSNP009050510098 chr12: 47981 CE3 Intergenic G A
homozygote
MACSNP009050510100 chr12: 48146 CE3 Intergenic A C
homozygote
MACSNP009050510104 chr12: 48427 CE3 Intergenic T G
homozygote
MACSNP009050510109 chr12: 48981 CE3 Intergenic G A
homozygote
MACSNP009050510125 chr12: 50515 CE3 Intergenic A G
heterozygote
MACSNP009050510141 chr12: 52133 CE3 ENSMMUG00000009615: CDS
C T
heterozygote