Filter SNPs Using Feature Selection

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334196 SNPs 1 of 33420 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP004071388318 chr17: 520117 TW1 ENSMMUG00000016560: Intron
G A
heterozygote
MACSNP004071388331 chr17: 520693 TW1 ENSMMUG00000016560: Intron
A C
heterozygote
MACSNP004071388334 chr17: 520876 TW1 ENSMMUG00000016560: Intron
G A
heterozygote
MACSNP004071388345 chr17: 521460 TW1 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP004071388347 chr17: 521552 TW1 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP004071388353 chr17: 521822 TW1 ENSMMUG00000016560: Intron
A T
homozygote
MACSNP004071388370 chr17: 522695 TW1 Intergenic A G
homozygote
MACSNP004071388391 chr17: 523141 TW1 Intergenic T C
homozygote
MACSNP004071388393 chr17: 523183 TW1 Intergenic C T
homozygote
MACSNP004071388395 chr17: 523260 TW1 Intergenic T G
homozygote