Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP006050510057 | chr12: 38443 | JM2 |
ENSMMUG00000009617: Intron |
C | G |
homozygote
|
MACSNP006050510067 | chr12: 39590 | JM2 | Intergenic | G | A |
homozygote
|
MACSNP006050510070 | chr12: 40345 | JM2 | Intergenic | G | A |
homozygote
|
MACSNP006050510072 | chr12: 40601 | JM2 | Intergenic | T | C |
homozygote
|
MACSNP006050510074 | chr12: 40777 | JM2 | Intergenic | C | T |
homozygote
|
MACSNP006050510088 | chr12: 47142 | JM2 | Intergenic | C | A |
homozygote
|
MACSNP006050510089 | chr12: 47162 | JM2 | Intergenic | G | T |
homozygote
|
MACSNP006050510098 | chr12: 47981 | JM2 | Intergenic | G | A |
homozygote
|
MACSNP006050510104 | chr12: 48427 | JM2 | Intergenic | T | G |
homozygote
|
MACSNP006050510110 | chr12: 49057 | JM2 | Intergenic | A | G |
homozygote
|