Filter SNVs Using Feature Selection

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577221 SNVs 1 of 57723 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011036100671 chr8: 395560 CE5 ENSMMUG00000011105: Intron
A T
heterozygote
MACSNP011036100676 chr8: 395610 CE5 ENSMMUG00000011105: Intron
C G
heterozygote
MACSNP011036100685 chr8: 395904 CE5 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP011036100686 chr8: 395921 CE5 ENSMMUG00000011105: Intron
A C
heterozygote
MACSNP011036100694 chr8: 396139 CE5 ENSMMUG00000011105: Intron
A G
heterozygote
MACSNP011036100697 chr8: 396155 CE5 ENSMMUG00000011105: Intron
T G
heterozygote
MACSNP011036100698 chr8: 396171 CE5 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP011036100702 chr8: 396349 CE5 ENSMMUG00000011105: Intron
A G
heterozygote
MACSNP011036100703 chr8: 396371 CE5 ENSMMUG00000011105: Intron
T C
homozygote
MACSNP011036100706 chr8: 396513 CE5 ENSMMUG00000011105: Intron
A G
heterozygote