Filter SNVs Using Feature Selection

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221577 SNVs 1 of 22158 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002050510057 chr12: 38443 CR2 ENSMMUG00000009617: Intron
C G
homozygote
MACSNP002050510067 chr12: 39590 CR2 Intergenic G A
homozygote
MACSNP002050510074 chr12: 40777 CR2 Intergenic C T
heterozygote
MACSNP002050510078 chr12: 45993 CR2 Intergenic G A
heterozygote
MACSNP002050510083 chr12: 46273 CR2 Intergenic T A
heterozygote
MACSNP002050510086 chr12: 47029 CR2 Intergenic C T
heterozygote
MACSNP002050510104 chr12: 48427 CR2 Intergenic T G
homozygote
MACSNP002050510109 chr12: 48981 CR2 Intergenic G A
heterozygote
MACSNP002050510120 chr12: 49898 CR2 Intergenic C T
heterozygote
MACSNP002050510127 chr12: 50574 CR2 Intergenic G A
heterozygote