Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP013050510057 | chr12: 38443 | TM2 |
ENSMMUG00000009617: Intron |
C | G |
homozygote
|
MACSNP013050510067 | chr12: 39590 | TM2 | Intergenic | G | A |
homozygote
|
MACSNP013050510071 | chr12: 40506 | TM2 | Intergenic | C | G |
homozygote
|
MACSNP013050510072 | chr12: 40601 | TM2 | Intergenic | T | C |
homozygote
|
MACSNP013050510074 | chr12: 40777 | TM2 | Intergenic | C | T |
homozygote
|
MACSNP013050510082 | chr12: 46233 | TM2 | Intergenic | A | G |
homozygote
|
MACSNP013050510084 | chr12: 46617 | TM2 | Intergenic | C | T |
homozygote
|
MACSNP013050510093 | chr12: 47314 | TM2 | Intergenic | C | T |
homozygote
|
MACSNP013050510098 | chr12: 47981 | TM2 | Intergenic | G | A |
homozygote
|
MACSNP013050510104 | chr12: 48427 | TM2 | Intergenic | T | G |
homozygote
|