Filter SNPs Using Feature Selection

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433465 SNPs 1 of 43347 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006039432775 chr8: 307378 JM2 ENSMMUG00000011105: Intron
C T
homozygote
MACSNP006039432782 chr8: 307633 JM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP006039432784 chr8: 307677 JM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP006039432795 chr8: 307900 JM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP006039432800 chr8: 308100 JM2 ENSMMUG00000011105: Intron
T C
homozygote
MACSNP006039432807 chr8: 308319 JM2 ENSMMUG00000011105: Intron
T G
homozygote
MACSNP006039432842 chr8: 309304 JM2 ENSMMUG00000011105: Intron
A C
homozygote
MACSNP006039432852 chr8: 309705 JM2 ENSMMUG00000011105: Intron
T A
homozygote
MACSNP006039432859 chr8: 309955 JM2 ENSMMUG00000011105: Intron
G T
homozygote
MACSNP006039432866 chr8: 310082 JM2 ENSMMUG00000011105: Intron
T C
homozygote