Filter SNPs Using Feature Selection

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436241 SNPs 1 of 43625 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP019071388341 chr17: 521270 LTM ENSMMUG00000016560: Intron
T C
homozygote
MACSNP019071388345 chr17: 521460 LTM ENSMMUG00000016560: Intron
C T
homozygote
MACSNP019071388347 chr17: 521552 LTM ENSMMUG00000016560: Intron
G T
homozygote
MACSNP019071388350 chr17: 521683 LTM ENSMMUG00000016560: Intron
C A
homozygote
MACSNP019071388357 chr17: 522022 LTM ENSMMUG00000016560: Intron
C T
homozygote
MACSNP019071388364 chr17: 522405 LTM Intergenic C A
heterozygote
MACSNP019071388366 chr17: 522584 LTM Intergenic C T
homozygote
MACSNP019071388370 chr17: 522695 LTM Intergenic A G
homozygote
MACSNP019071388371 chr17: 522702 LTM Intergenic G A
homozygote
MACSNP019071388373 chr17: 522800 LTM Intergenic T C
homozygote