Filter SNVs Using Feature Selection

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401002 SNVs 1 of 40101 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP010050510057 chr12: 38443 CE4 ENSMMUG00000009617: Intron
C G
homozygote
MACSNP010050510067 chr12: 39590 CE4 Intergenic G A
homozygote
MACSNP010050510070 chr12: 40345 CE4 Intergenic G A
heterozygote
MACSNP010050510072 chr12: 40601 CE4 Intergenic T C
homozygote
MACSNP010050510084 chr12: 46617 CE4 Intergenic C T
homozygote
MACSNP010050510098 chr12: 47981 CE4 Intergenic G A
homozygote
MACSNP010050510100 chr12: 48146 CE4 Intergenic A C
homozygote
MACSNP010050510104 chr12: 48427 CE4 Intergenic T G
homozygote
MACSNP010050510114 chr12: 49498 CE4 Intergenic C T
heterozygote
MACSNP010050510115 chr12: 49504 CE4 Intergenic G A
heterozygote