Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP001072229809 | chr20: 375 | CR1 | Intergenic | G | A |
heterozygote
|
MACSNP001072229837 | chr20: 5681 | CR1 |
ENSMMUG00000000586: Intron |
G | A |
heterozygote
|
MACSNP001072229845 | chr20: 6063 | CR1 |
ENSMMUG00000000586: Intron |
A | T |
homozygote
|
MACSNP001072229873 | chr20: 8700 | CR1 |
ENSMMUG00000000586: Intron |
C | G |
homozygote
|
MACSNP001072229885 | chr20: 9190 | CR1 |
ENSMMUG00000000586: Intron ENSMMUG00000047475: 5'UTR |
G | A |
heterozygote
|
MACSNP001072229915 | chr20: 10349 | CR1 |
ENSMMUG00000047475: Intron |
A | C |
homozygote
|
MACSNP001072229918 | chr20: 10450 | CR1 |
ENSMMUG00000047475: Intron |
C | A |
homozygote
|
MACSNP001072229920 | chr20: 10514 | CR1 |
ENSMMUG00000047475: Intron |
A | G |
homozygote
|
MACSNP001072229931 | chr20: 10864 | CR1 |
ENSMMUG00000047475: Intron |
G | C |
heterozygote
|
MACSNP001072229932 | chr20: 10886 | CR1 |
ENSMMUG00000047475: Intron |
G | A |
heterozygote
|