Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP007036100650 | chr8: 234576 | CE1 |
ENSMMUG00000020598: Intron |
C | T |
heterozygote
|
MACSNP007036100651 | chr8: 234602 | CE1 |
ENSMMUG00000020598: Intron |
G | C |
heterozygote
|
MACSNP007036100672 | chr8: 395584 | CE1 |
ENSMMUG00000011105: Intron |
C | T |
heterozygote
|
MACSNP007036100678 | chr8: 395649 | CE1 |
ENSMMUG00000011105: Intron |
C | T |
heterozygote
|
MACSNP007036100685 | chr8: 395904 | CE1 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP007036100688 | chr8: 395963 | CE1 |
ENSMMUG00000011105: Intron |
G | A |
heterozygote
|
MACSNP007036100691 | chr8: 396075 | CE1 |
ENSMMUG00000011105: Intron |
T | G |
heterozygote
|
MACSNP007036100692 | chr8: 396091 | CE1 |
ENSMMUG00000011105: Intron |
A | G |
heterozygote
|
MACSNP007036100696 | chr8: 396152 | CE1 |
ENSMMUG00000011105: Intron |
G | A |
heterozygote
|
MACSNP007036100698 | chr8: 396171 | CE1 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|