Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP011072229813 | chr20: 840 | CE5 | Intergenic | G | A |
heterozygote
|
MACSNP011072229819 | chr20: 1391 | CE5 | Intergenic | T | C |
homozygote
|
MACSNP011072229827 | chr20: 5304 | CE5 |
ENSMMUG00000000586: Intron |
A | G |
homozygote
|
MACSNP011072229835 | chr20: 5667 | CE5 |
ENSMMUG00000000586: Intron |
A | G |
homozygote
|
MACSNP011072229838 | chr20: 5710 | CE5 |
ENSMMUG00000000586: Intron |
C | G |
homozygote
|
MACSNP011072229840 | chr20: 5806 | CE5 |
ENSMMUG00000000586: Intron |
C | T |
homozygote
|
MACSNP011072229869 | chr20: 8567 | CE5 |
ENSMMUG00000000586: Intron |
A | C |
heterozygote
|
MACSNP011072229886 | chr20: 9236 | CE5 |
ENSMMUG00000000586: Intron ENSMMUG00000047475: 5'UTR |
G | A |
homozygote
|
MACSNP011072229931 | chr20: 10864 | CE5 |
ENSMMUG00000047475: Intron |
G | C |
homozygote
|
MACSNP011072229932 | chr20: 10886 | CE5 |
ENSMMUG00000047475: Intron |
G | A |
homozygote
|