Filter SNPs Using Feature Selection

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519156 SNPs 1 of 51916 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP017071388314 chr17: 519976 PM1 ENSMMUG00000016560: Intron
G A
heterozygote
MACSNP017071388316 chr17: 520021 PM1 ENSMMUG00000016560: Intron
C T
heterozygote
MACSNP017071388321 chr17: 520196 PM1 ENSMMUG00000016560: Intron
C T
heterozygote
MACSNP017071388334 chr17: 520876 PM1 ENSMMUG00000016560: Intron
G A
heterozygote
MACSNP017071388341 chr17: 521270 PM1 ENSMMUG00000016560: Intron
T C
heterozygote
MACSNP017071388345 chr17: 521460 PM1 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP017071388347 chr17: 521552 PM1 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP017071388350 chr17: 521683 PM1 ENSMMUG00000016560: Intron
C A
homozygote
MACSNP017071388355 chr17: 521844 PM1 ENSMMUG00000016560: Intron
T G
heterozygote
MACSNP017071388370 chr17: 522695 PM1 Intergenic A G
homozygote