Filter SNVs Using Feature Selection

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302968 SNVs 1 of 30297 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP005050510057 chr12: 38443 JM1 ENSMMUG00000009617: Intron
C G
homozygote
MACSNP005050510062 chr12: 38913 JM1 ENSMMUG00000009617: Intron
C T
heterozygote
MACSNP005050510067 chr12: 39590 JM1 Intergenic G A
homozygote
MACSNP005050510070 chr12: 40345 JM1 Intergenic G A
homozygote
MACSNP005050510072 chr12: 40601 JM1 Intergenic T C
homozygote
MACSNP005050510074 chr12: 40777 JM1 Intergenic C T
homozygote
MACSNP005050510088 chr12: 47142 JM1 Intergenic C A
homozygote
MACSNP005050510089 chr12: 47162 JM1 Intergenic G T
homozygote
MACSNP005050510090 chr12: 47171 JM1 Intergenic T A
homozygote
MACSNP005050510097 chr12: 47701 JM1 Intergenic C T
heterozygote