Filter SNVs Using Feature Selection

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613272 SNVs 1 of 61328 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP014036100631 chr8: 223081 AM1 Intergenic G A
homozygote
MACSNP014036100673 chr8: 395585 AM1 ENSMMUG00000011105: Intron
G A
heterozygote
MACSNP014036100677 chr8: 395629 AM1 ENSMMUG00000011105: Intron
G A
heterozygote
MACSNP014036100680 chr8: 395692 AM1 ENSMMUG00000011105: Intron
G A
heterozygote
MACSNP014036100685 chr8: 395904 AM1 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP014036100698 chr8: 396171 AM1 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP014036100700 chr8: 396287 AM1 ENSMMUG00000011105: Intron
T C
heterozygote
MACSNP014036100701 chr8: 396338 AM1 ENSMMUG00000011105: Intron
G A
heterozygote
MACSNP014036100703 chr8: 396371 AM1 ENSMMUG00000011105: Intron
T C
homozygote
MACSNP014036100710 chr8: 396590 AM1 ENSMMUG00000011105: Intron
T G
homozygote