Filter SNPs Using Feature Selection

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429064 SNPs 1 of 42907 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011071388320 chr17: 520170 CE5 ENSMMUG00000016560: Intron
G A
homozygote
MACSNP011071388345 chr17: 521460 CE5 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP011071388347 chr17: 521552 CE5 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP011071388351 chr17: 521744 CE5 ENSMMUG00000016560: Intron
G A
homozygote
MACSNP011071388352 chr17: 521762 CE5 ENSMMUG00000016560: Intron
G A
homozygote
MACSNP011071388369 chr17: 522629 CE5 Intergenic G A
homozygote
MACSNP011071388370 chr17: 522695 CE5 Intergenic A G
homozygote
MACSNP011071388383 chr17: 522994 CE5 Intergenic A G
heterozygote
MACSNP011071388385 chr17: 523001 CE5 Intergenic G A
heterozygote
MACSNP011071388386 chr17: 523030 CE5 Intergenic G C
homozygote