Filter SNPs Using Feature Selection

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462317 SNPs 1 of 46232 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP005039432775 chr8: 307378 JM1 ENSMMUG00000011105: Intron
C T
homozygote
MACSNP005039432782 chr8: 307633 JM1 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP005039432795 chr8: 307900 JM1 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP005039432796 chr8: 308000 JM1 ENSMMUG00000011105: Intron
G A
heterozygote
MACSNP005039432800 chr8: 308100 JM1 ENSMMUG00000011105: Intron
T C
homozygote
MACSNP005039432807 chr8: 308319 JM1 ENSMMUG00000011105: Intron
T G
homozygote
MACSNP005039432833 chr8: 309089 JM1 ENSMMUG00000011105: Intron
T C
heterozygote
MACSNP005039432842 chr8: 309304 JM1 ENSMMUG00000011105: Intron
A C
homozygote
MACSNP005039432852 chr8: 309705 JM1 ENSMMUG00000011105: Intron
T A
homozygote
MACSNP005039432859 chr8: 309955 JM1 ENSMMUG00000011105: Intron
G T
homozygote