Filter SNVs Using Feature Selection

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583613 SNVs 1 of 58362 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP007036100650 chr8: 234576 CE1 ENSMMUG00000020598: Intron
C T
heterozygote
MACSNP007036100651 chr8: 234602 CE1 ENSMMUG00000020598: Intron
G C
heterozygote
MACSNP007036100672 chr8: 395584 CE1 ENSMMUG00000011105: Intron
C T
heterozygote
MACSNP007036100678 chr8: 395649 CE1 ENSMMUG00000011105: Intron
C T
heterozygote
MACSNP007036100685 chr8: 395904 CE1 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP007036100688 chr8: 395963 CE1 ENSMMUG00000011105: Intron
G A
heterozygote
MACSNP007036100691 chr8: 396075 CE1 ENSMMUG00000011105: Intron
T G
heterozygote
MACSNP007036100692 chr8: 396091 CE1 ENSMMUG00000011105: Intron
A G
heterozygote
MACSNP007036100696 chr8: 396152 CE1 ENSMMUG00000011105: Intron
G A
heterozygote
MACSNP007036100698 chr8: 396171 CE1 ENSMMUG00000011105: Intron
A G
homozygote