Filter SNPs Using Feature Selection

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241317 SNPs 1 of 24132 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002071388329 chr17: 520650 CR2 ENSMMUG00000016560: Intron
C T
heterozygote
MACSNP002071388338 chr17: 520962 CR2 ENSMMUG00000016560: Intron
G T
heterozygote
MACSNP002071388345 chr17: 521460 CR2 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP002071388347 chr17: 521552 CR2 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP002071388365 chr17: 522507 CR2 Intergenic G A
homozygote
MACSNP002071388395 chr17: 523260 CR2 Intergenic T G
homozygote
MACSNP002071388400 chr17: 523402 CR2 Intergenic G C
homozygote
MACSNP002071388402 chr17: 523546 CR2 Intergenic C T
homozygote
MACSNP002071388427 chr17: 524542 CR2 Intergenic T C
homozygote
MACSNP002071388432 chr17: 524746 CR2 Intergenic T C
homozygote