Filter SNVs Using Feature Selection

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423764 SNVs 1 of 42377 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007050510057 chr12: 38443 CE1 ENSMMUG00000009617: Intron
C G
homozygote
MACSNP007050510067 chr12: 39590 CE1 Intergenic G A
homozygote
MACSNP007050510072 chr12: 40601 CE1 Intergenic T C
homozygote
MACSNP007050510074 chr12: 40777 CE1 Intergenic C T
homozygote
MACSNP007050510084 chr12: 46617 CE1 Intergenic C T
homozygote
MACSNP007050510085 chr12: 46997 CE1 Intergenic C T
homozygote
MACSNP007050510092 chr12: 47289 CE1 Intergenic C G
heterozygote
MACSNP007050510098 chr12: 47981 CE1 Intergenic G A
homozygote
MACSNP007050510100 chr12: 48146 CE1 Intergenic A C
homozygote
MACSNP007050510104 chr12: 48427 CE1 Intergenic T G
homozygote