Filter SNVs Using Feature Selection

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391508 SNVs 1 of 39151 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006036100678 chr8: 395649 JM2 ENSMMUG00000011105: Intron
C T
homozygote
MACSNP006036100685 chr8: 395904 JM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP006036100687 chr8: 395948 JM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP006036100698 chr8: 396171 JM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP006036100703 chr8: 396371 JM2 ENSMMUG00000011105: Intron
T C
homozygote
MACSNP006036100710 chr8: 396590 JM2 ENSMMUG00000011105: Intron
T G
homozygote
MACSNP006036100745 chr8: 397575 JM2 ENSMMUG00000011105: Intron
A C
homozygote
MACSNP006036100755 chr8: 397976 JM2 ENSMMUG00000011105: Intron
T A
homozygote
MACSNP006036100762 chr8: 398226 JM2 ENSMMUG00000011105: Intron
G T
homozygote
MACSNP006036100768 chr8: 398353 JM2 ENSMMUG00000011105: Intron
T C
homozygote