Filter SNPs Using Feature Selection

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496951 SNPs 1 of 49696 Pages
Individual SNP ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010062033227 chr14: 3686 CE4 Intergenic A G
homozygote
MACSNP010062033245 chr14: 4416 CE4 Intergenic A T
homozygote
MACSNP010062033247 chr14: 4511 CE4 ENSMMUG00000011501: Exon
C T
homozygote
MACSNP010062033256 chr14: 4749 CE4 ENSMMUG00000011501: Intron
C G
homozygote
MACSNP010062033261 chr14: 5013 CE4 ENSMMUG00000011501: CDS
T C
homozygote
MACSNP010062033274 chr14: 5372 CE4 ENSMMUG00000011501: Intron
A T
homozygote
MACSNP010062033275 chr14: 5401 CE4 ENSMMUG00000011501: Intron
T C
homozygote
MACSNP010062033280 chr14: 5481 CE4 ENSMMUG00000011501: Intron
G T
homozygote
MACSNP010062033281 chr14: 5507 CE4 ENSMMUG00000011501: Intron
T C
homozygote
MACSNP010062033300 chr14: 6138 CE4 Intergenic T C
homozygote