Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP005050510057 | chr12: 38443 | JM1 |
ENSMMUG00000009617: Intron |
C | G |
homozygote
|
MACSNP005050510062 | chr12: 38913 | JM1 |
ENSMMUG00000009617: Intron |
C | T |
heterozygote
|
MACSNP005050510067 | chr12: 39590 | JM1 | Intergenic | G | A |
homozygote
|
MACSNP005050510070 | chr12: 40345 | JM1 | Intergenic | G | A |
homozygote
|
MACSNP005050510072 | chr12: 40601 | JM1 | Intergenic | T | C |
homozygote
|
MACSNP005050510074 | chr12: 40777 | JM1 | Intergenic | C | T |
homozygote
|
MACSNP005050510088 | chr12: 47142 | JM1 | Intergenic | C | A |
homozygote
|
MACSNP005050510089 | chr12: 47162 | JM1 | Intergenic | G | T |
homozygote
|
MACSNP005050510090 | chr12: 47171 | JM1 | Intergenic | T | A |
homozygote
|
MACSNP005050510097 | chr12: 47701 | JM1 | Intergenic | C | T |
heterozygote
|