Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP009050510057 | chr12: 38443 | CE3 |
ENSMMUG00000009617: Intron |
C | G |
homozygote
|
MACSNP009050510067 | chr12: 39590 | CE3 | Intergenic | G | A |
homozygote
|
MACSNP009050510072 | chr12: 40601 | CE3 | Intergenic | T | C |
homozygote
|
MACSNP009050510084 | chr12: 46617 | CE3 | Intergenic | C | T |
homozygote
|
MACSNP009050510098 | chr12: 47981 | CE3 | Intergenic | G | A |
homozygote
|
MACSNP009050510100 | chr12: 48146 | CE3 | Intergenic | A | C |
homozygote
|
MACSNP009050510104 | chr12: 48427 | CE3 | Intergenic | T | G |
homozygote
|
MACSNP009050510109 | chr12: 48981 | CE3 | Intergenic | G | A |
homozygote
|
MACSNP009050510125 | chr12: 50515 | CE3 | Intergenic | A | G |
heterozygote
|
MACSNP009050510141 | chr12: 52133 | CE3 |
ENSMMUG00000009615: CDS |
C | T |
heterozygote
|