Filter SNPs Using Feature Selection

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590622 SNPs 1 of 59063 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016039432760 chr8: 307168 SM2 ENSMMUG00000011105: Intron
G A
homozygote
MACSNP016039432770 chr8: 307314 SM2 ENSMMUG00000011105: Intron
G A
homozygote
MACSNP016039432782 chr8: 307633 SM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP016039432795 chr8: 307900 SM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP016039432798 chr8: 308067 SM2 ENSMMUG00000011105: Intron
G A
homozygote
MACSNP016039432800 chr8: 308100 SM2 ENSMMUG00000011105: Intron
T C
homozygote
MACSNP016039432807 chr8: 308319 SM2 ENSMMUG00000011105: Intron
T G
homozygote
MACSNP016039432820 chr8: 308729 SM2 ENSMMUG00000011105: Intron
G A
homozygote
MACSNP016039432821 chr8: 308777 SM2 ENSMMUG00000011105: Intron
T C
homozygote
MACSNP016039432829 chr8: 308960 SM2 ENSMMUG00000011105: Intron
G T
homozygote