Filter SNPs Using Feature Selection

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516124 SNPs 1 of 51613 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP018071388312 chr17: 519956 PM2 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP018071388314 chr17: 519976 PM2 ENSMMUG00000016560: Intron
G A
heterozygote
MACSNP018071388316 chr17: 520021 PM2 ENSMMUG00000016560: Intron
C T
heterozygote
MACSNP018071388341 chr17: 521270 PM2 ENSMMUG00000016560: Intron
T C
heterozygote
MACSNP018071388345 chr17: 521460 PM2 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP018071388347 chr17: 521552 PM2 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP018071388350 chr17: 521683 PM2 ENSMMUG00000016560: Intron
C A
homozygote
MACSNP018071388355 chr17: 521844 PM2 ENSMMUG00000016560: Intron
T G
heterozygote
MACSNP018071388357 chr17: 522022 PM2 ENSMMUG00000016560: Intron
C T
heterozygote
MACSNP018071388369 chr17: 522629 PM2 Intergenic G A
heterozygote