Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP011036100671 | chr8: 395560 | CE5 |
ENSMMUG00000011105: Intron |
A | T |
heterozygote
|
MACSNP011036100676 | chr8: 395610 | CE5 |
ENSMMUG00000011105: Intron |
C | G |
heterozygote
|
MACSNP011036100685 | chr8: 395904 | CE5 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP011036100686 | chr8: 395921 | CE5 |
ENSMMUG00000011105: Intron |
A | C |
heterozygote
|
MACSNP011036100694 | chr8: 396139 | CE5 |
ENSMMUG00000011105: Intron |
A | G |
heterozygote
|
MACSNP011036100697 | chr8: 396155 | CE5 |
ENSMMUG00000011105: Intron |
T | G |
heterozygote
|
MACSNP011036100698 | chr8: 396171 | CE5 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP011036100702 | chr8: 396349 | CE5 |
ENSMMUG00000011105: Intron |
A | G |
heterozygote
|
MACSNP011036100703 | chr8: 396371 | CE5 |
ENSMMUG00000011105: Intron |
T | C |
homozygote
|
MACSNP011036100706 | chr8: 396513 | CE5 |
ENSMMUG00000011105: Intron |
A | G |
heterozygote
|