Filter SNPs Using Feature Selection

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441820 SNPs 1 of 44182 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007071388318 chr17: 520117 CE1 ENSMMUG00000016560: Intron
G A
homozygote
MACSNP007071388324 chr17: 520387 CE1 ENSMMUG00000016560: CDS
T C
homozygote
MACSNP007071388345 chr17: 521460 CE1 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP007071388347 chr17: 521552 CE1 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP007071388353 chr17: 521822 CE1 ENSMMUG00000016560: Intron
A T
homozygote
MACSNP007071388365 chr17: 522507 CE1 Intergenic G A
heterozygote
MACSNP007071388370 chr17: 522695 CE1 Intergenic A G
homozygote
MACSNP007071388391 chr17: 523141 CE1 Intergenic T C
homozygote
MACSNP007071388392 chr17: 523149 CE1 Intergenic G A
homozygote
MACSNP007071388393 chr17: 523183 CE1 Intergenic C T
homozygote