Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP011050510057 | chr12: 38443 | CE5 |
ENSMMUG00000009617: Intron |
C | G |
homozygote
|
MACSNP011050510067 | chr12: 39590 | CE5 | Intergenic | G | A |
homozygote
|
MACSNP011050510070 | chr12: 40345 | CE5 | Intergenic | G | A |
heterozygote
|
MACSNP011050510072 | chr12: 40601 | CE5 | Intergenic | T | C |
homozygote
|
MACSNP011050510074 | chr12: 40777 | CE5 | Intergenic | C | T |
heterozygote
|
MACSNP011050510084 | chr12: 46617 | CE5 | Intergenic | C | T |
homozygote
|
MACSNP011050510085 | chr12: 46997 | CE5 | Intergenic | C | T |
heterozygote
|
MACSNP011050510100 | chr12: 48146 | CE5 | Intergenic | A | C |
heterozygote
|
MACSNP011050510104 | chr12: 48427 | CE5 | Intergenic | T | G |
homozygote
|
MACSNP011050510107 | chr12: 48880 | CE5 | Intergenic | A | G |
heterozygote
|