Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP015050510057 | chr12: 38443 | SM1 |
ENSMMUG00000009617: Intron |
C | G |
homozygote
|
MACSNP015050510067 | chr12: 39590 | SM1 | Intergenic | G | A |
homozygote
|
MACSNP015050510084 | chr12: 46617 | SM1 | Intergenic | C | T |
homozygote
|
MACSNP015050510088 | chr12: 47142 | SM1 | Intergenic | C | A |
heterozygote
|
MACSNP015050510098 | chr12: 47981 | SM1 | Intergenic | G | A |
homozygote
|
MACSNP015050510099 | chr12: 48081 | SM1 | Intergenic | A | G |
homozygote
|
MACSNP015050510104 | chr12: 48427 | SM1 | Intergenic | T | G |
homozygote
|
MACSNP015050510106 | chr12: 48739 | SM1 | Intergenic | C | T |
homozygote
|
MACSNP015050510112 | chr12: 49145 | SM1 | Intergenic | T | C |
homozygote
|
MACSNP015050510124 | chr12: 50461 | SM1 | Intergenic | C | T |
homozygote
|