Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP010050510057 | chr12: 38443 | CE4 |
ENSMMUG00000009617: Intron |
C | G |
homozygote
|
MACSNP010050510067 | chr12: 39590 | CE4 | Intergenic | G | A |
homozygote
|
MACSNP010050510070 | chr12: 40345 | CE4 | Intergenic | G | A |
heterozygote
|
MACSNP010050510072 | chr12: 40601 | CE4 | Intergenic | T | C |
homozygote
|
MACSNP010050510084 | chr12: 46617 | CE4 | Intergenic | C | T |
homozygote
|
MACSNP010050510098 | chr12: 47981 | CE4 | Intergenic | G | A |
homozygote
|
MACSNP010050510100 | chr12: 48146 | CE4 | Intergenic | A | C |
homozygote
|
MACSNP010050510104 | chr12: 48427 | CE4 | Intergenic | T | G |
homozygote
|
MACSNP010050510114 | chr12: 49498 | CE4 | Intergenic | C | T |
heterozygote
|
MACSNP010050510115 | chr12: 49504 | CE4 | Intergenic | G | A |
heterozygote
|