Filter SNVs Using Feature Selection

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382882 SNVs 1 of 38289 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013050510057 chr12: 38443 TM2 ENSMMUG00000009617: Intron
C G
homozygote
MACSNP013050510067 chr12: 39590 TM2 Intergenic G A
homozygote
MACSNP013050510071 chr12: 40506 TM2 Intergenic C G
homozygote
MACSNP013050510072 chr12: 40601 TM2 Intergenic T C
homozygote
MACSNP013050510074 chr12: 40777 TM2 Intergenic C T
homozygote
MACSNP013050510082 chr12: 46233 TM2 Intergenic A G
homozygote
MACSNP013050510084 chr12: 46617 TM2 Intergenic C T
homozygote
MACSNP013050510093 chr12: 47314 TM2 Intergenic C T
homozygote
MACSNP013050510098 chr12: 47981 TM2 Intergenic G A
homozygote
MACSNP013050510104 chr12: 48427 TM2 Intergenic T G
homozygote