Filter SNPs Using Feature Selection

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446209 SNPs 1 of 44621 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010071388320 chr17: 520170 CE4 ENSMMUG00000016560: Intron
G A
heterozygote
MACSNP010071388341 chr17: 521270 CE4 ENSMMUG00000016560: Intron
T C
heterozygote
MACSNP010071388345 chr17: 521460 CE4 ENSMMUG00000016560: Intron
C T
homozygote
MACSNP010071388347 chr17: 521552 CE4 ENSMMUG00000016560: Intron
G T
homozygote
MACSNP010071388350 chr17: 521683 CE4 ENSMMUG00000016560: Intron
C A
homozygote
MACSNP010071388351 chr17: 521744 CE4 ENSMMUG00000016560: Intron
G A
heterozygote
MACSNP010071388352 chr17: 521762 CE4 ENSMMUG00000016560: Intron
G A
heterozygote
MACSNP010071388358 chr17: 522106 CE4 ENSMMUG00000016560: Intron
C A
heterozygote
MACSNP010071388362 chr17: 522257 CE4 ENSMMUG00000016560: CDS
C T
heterozygote
MACSNP010071388370 chr17: 522695 CE4 Intergenic A G
homozygote