Filter SNPs Using Feature Selection

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369623 SNPs 1 of 36963 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013071388313 chr17: 519957 TM2 ENSMMUG00000016560: Intron
G A
homozygote
MACSNP013071388315 chr17: 520018 TM2 ENSMMUG00000016560: Intron
A G
homozygote
MACSNP013071388333 chr17: 520857 TM2 ENSMMUG00000016560: Intron
T A
homozygote
MACSNP013071388345 chr17: 521460 TM2 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP013071388346 chr17: 521482 TM2 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP013071388347 chr17: 521552 TM2 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP013071388350 chr17: 521683 TM2 ENSMMUG00000016560: Intron
C A
homozygote
MACSNP013071388367 chr17: 522605 TM2 Intergenic C T
homozygote
MACSNP013071388370 chr17: 522695 TM2 Intergenic A G
homozygote
MACSNP013071388393 chr17: 523183 TM2 Intergenic C T
homozygote