Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP014036100631 | chr8: 223081 | AM1 | Intergenic | G | A |
homozygote
|
MACSNP014036100673 | chr8: 395585 | AM1 |
ENSMMUG00000011105: Intron |
G | A |
heterozygote
|
MACSNP014036100677 | chr8: 395629 | AM1 |
ENSMMUG00000011105: Intron |
G | A |
heterozygote
|
MACSNP014036100680 | chr8: 395692 | AM1 |
ENSMMUG00000011105: Intron |
G | A |
heterozygote
|
MACSNP014036100685 | chr8: 395904 | AM1 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP014036100698 | chr8: 396171 | AM1 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP014036100700 | chr8: 396287 | AM1 |
ENSMMUG00000011105: Intron |
T | C |
heterozygote
|
MACSNP014036100701 | chr8: 396338 | AM1 |
ENSMMUG00000011105: Intron |
G | A |
heterozygote
|
MACSNP014036100703 | chr8: 396371 | AM1 |
ENSMMUG00000011105: Intron |
T | C |
homozygote
|
MACSNP014036100710 | chr8: 396590 | AM1 |
ENSMMUG00000011105: Intron |
T | G |
homozygote
|