Filter SNVs Using Feature Selection

Show entries
313748 SNVs 1 of 31375 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP019072229811 chr20: 618 LM1 Intergenic C T
homozygote
MACSNP019072229829 chr20: 5346 LM1 ENSMMUG00000000586: Intron
C T
homozygote
MACSNP019072229840 chr20: 5806 LM1 ENSMMUG00000000586: Intron
C T
homozygote
MACSNP019072229846 chr20: 6125 LM1 ENSMMUG00000000586: Intron
T A
heterozygote
MACSNP019072229853 chr20: 7211 LM1 ENSMMUG00000000586: Intron
T A
homozygote
MACSNP019072229870 chr20: 8640 LM1 ENSMMUG00000000586: Intron
A G
heterozygote
MACSNP019072229873 chr20: 8700 LM1 ENSMMUG00000000586: Intron
C G
homozygote
MACSNP019072229882 chr20: 9006 LM1 ENSMMUG00000000586: Intron
G C
homozygote
MACSNP019072229889 chr20: 9422 LM1 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
A C
homozygote
MACSNP019072229891 chr20: 9466 LM1 ENSMMUG00000000586: Intron
ENSMMUG00000047475: 5'UTR
A G
homozygote