Filter SNPs Using Feature Selection

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399925 SNPs 1 of 39993 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016071388313 chr17: 519957 SM2 ENSMMUG00000016560: Intron
G A
homozygote
MACSNP016071388315 chr17: 520018 SM2 ENSMMUG00000016560: Intron
A G
homozygote
MACSNP016071388317 chr17: 520044 SM2 ENSMMUG00000016560: Intron
G A
heterozygote
MACSNP016071388330 chr17: 520691 SM2 ENSMMUG00000016560: Intron
G C
heterozygote
MACSNP016071388333 chr17: 520857 SM2 ENSMMUG00000016560: Intron
T A
homozygote
MACSNP016071388345 chr17: 521460 SM2 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP016071388347 chr17: 521552 SM2 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP016071388350 chr17: 521683 SM2 ENSMMUG00000016560: Intron
C A
homozygote
MACSNP016071388354 chr17: 521828 SM2 ENSMMUG00000016560: Intron
A T
heterozygote
MACSNP016071388370 chr17: 522695 SM2 Intergenic A G
homozygote