Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP007050510057 | chr12: 38443 | CE1 |
ENSMMUG00000009617: Intron |
C | G |
homozygote
|
MACSNP007050510067 | chr12: 39590 | CE1 | Intergenic | G | A |
homozygote
|
MACSNP007050510072 | chr12: 40601 | CE1 | Intergenic | T | C |
homozygote
|
MACSNP007050510074 | chr12: 40777 | CE1 | Intergenic | C | T |
homozygote
|
MACSNP007050510084 | chr12: 46617 | CE1 | Intergenic | C | T |
homozygote
|
MACSNP007050510085 | chr12: 46997 | CE1 | Intergenic | C | T |
homozygote
|
MACSNP007050510092 | chr12: 47289 | CE1 | Intergenic | C | G |
heterozygote
|
MACSNP007050510098 | chr12: 47981 | CE1 | Intergenic | G | A |
homozygote
|
MACSNP007050510100 | chr12: 48146 | CE1 | Intergenic | A | C |
homozygote
|
MACSNP007050510104 | chr12: 48427 | CE1 | Intergenic | T | G |
homozygote
|