Filter SNPs Using Feature Selection

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356654 SNPs 1 of 35666 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP001071388318 chr17: 520117 CR1 ENSMMUG00000016560: Intron
G A
homozygote
MACSNP001071388329 chr17: 520650 CR1 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP001071388345 chr17: 521460 CR1 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP001071388347 chr17: 521552 CR1 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP001071388353 chr17: 521822 CR1 ENSMMUG00000016560: Intron
A T
homozygote
MACSNP001071388370 chr17: 522695 CR1 Intergenic A G
homozygote
MACSNP001071388386 chr17: 523030 CR1 Intergenic G C
heterozygote
MACSNP001071388391 chr17: 523141 CR1 Intergenic T C
homozygote
MACSNP001071388393 chr17: 523183 CR1 Intergenic C T
homozygote
MACSNP001071388395 chr17: 523260 CR1 Intergenic T G
homozygote