Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP007072229809 | chr20: 375 | CE1 | Intergenic | G | A |
homozygote
|
MACSNP007072229816 | chr20: 1213 | CE1 | Intergenic | C | T |
heterozygote
|
MACSNP007072229819 | chr20: 1391 | CE1 | Intergenic | T | C |
homozygote
|
MACSNP007072229827 | chr20: 5304 | CE1 |
ENSMMUG00000000586: Intron |
A | G |
homozygote
|
MACSNP007072229835 | chr20: 5667 | CE1 |
ENSMMUG00000000586: Intron |
A | G |
homozygote
|
MACSNP007072229838 | chr20: 5710 | CE1 |
ENSMMUG00000000586: Intron |
C | G |
homozygote
|
MACSNP007072229840 | chr20: 5806 | CE1 |
ENSMMUG00000000586: Intron |
C | T |
homozygote
|
MACSNP007072229886 | chr20: 9236 | CE1 |
ENSMMUG00000000586: Intron ENSMMUG00000047475: 5'UTR |
G | A |
homozygote
|
MACSNP007072229893 | chr20: 9635 | CE1 |
ENSMMUG00000000586: CDS ENSMMUG00000047475: 5'UTR |
C | T |
homozygote
|
MACSNP007072229894 | chr20: 9696 | CE1 |
ENSMMUG00000000586: 5'UTR ENSMMUG00000047475: 5'UTR |
C | T |
homozygote
|