Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP008072229819 | chr20: 1391 | CE2 | Intergenic | T | C |
homozygote
|
MACSNP008072229823 | chr20: 4858 | CE2 |
ENSMMUG00000000586: Intron |
C | G |
heterozygote
|
MACSNP008072229827 | chr20: 5304 | CE2 |
ENSMMUG00000000586: Intron |
A | G |
homozygote
|
MACSNP008072229835 | chr20: 5667 | CE2 |
ENSMMUG00000000586: Intron |
A | G |
homozygote
|
MACSNP008072229855 | chr20: 7405 | CE2 |
ENSMMUG00000000586: CDS |
C | G |
heterozygote
|
MACSNP008072229856 | chr20: 7422 | CE2 |
ENSMMUG00000000586: CDS |
C | A |
heterozygote
|
MACSNP008072229863 | chr20: 8052 | CE2 |
ENSMMUG00000000586: Intron |
C | G |
homozygote
|
MACSNP008072229886 | chr20: 9236 | CE2 |
ENSMMUG00000000586: Intron ENSMMUG00000047475: 5'UTR |
G | A |
homozygote
|
MACSNP008072229894 | chr20: 9696 | CE2 |
ENSMMUG00000000586: 5'UTR ENSMMUG00000047475: 5'UTR |
C | T |
homozygote
|
MACSNP008072229915 | chr20: 10349 | CE2 |
ENSMMUG00000047475: Intron |
A | C |
homozygote
|