Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP019072229811 | chr20: 618 | LM1 | Intergenic | C | T |
homozygote
|
MACSNP019072229829 | chr20: 5346 | LM1 |
ENSMMUG00000000586: Intron |
C | T |
homozygote
|
MACSNP019072229840 | chr20: 5806 | LM1 |
ENSMMUG00000000586: Intron |
C | T |
homozygote
|
MACSNP019072229846 | chr20: 6125 | LM1 |
ENSMMUG00000000586: Intron |
T | A |
heterozygote
|
MACSNP019072229853 | chr20: 7211 | LM1 |
ENSMMUG00000000586: Intron |
T | A |
homozygote
|
MACSNP019072229870 | chr20: 8640 | LM1 |
ENSMMUG00000000586: Intron |
A | G |
heterozygote
|
MACSNP019072229873 | chr20: 8700 | LM1 |
ENSMMUG00000000586: Intron |
C | G |
homozygote
|
MACSNP019072229882 | chr20: 9006 | LM1 |
ENSMMUG00000000586: Intron |
G | C |
homozygote
|
MACSNP019072229889 | chr20: 9422 | LM1 |
ENSMMUG00000000586: Intron ENSMMUG00000047475: 5'UTR |
A | C |
homozygote
|
MACSNP019072229891 | chr20: 9466 | LM1 |
ENSMMUG00000000586: Intron ENSMMUG00000047475: 5'UTR |
A | G |
homozygote
|