Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP016072229808 | chr20: 325 | SM2 | Intergenic | G | A |
heterozygote
|
MACSNP016072229821 | chr20: 4827 | SM2 |
ENSMMUG00000000586: Intron |
T | A |
heterozygote
|
MACSNP016072229824 | chr20: 5161 | SM2 |
ENSMMUG00000000586: Intron |
G | T |
heterozygote
|
MACSNP016072229830 | chr20: 5371 | SM2 |
ENSMMUG00000000586: Intron |
T | C |
heterozygote
|
MACSNP016072229832 | chr20: 5475 | SM2 |
ENSMMUG00000000586: Intron |
T | C |
heterozygote
|
MACSNP016072229840 | chr20: 5806 | SM2 |
ENSMMUG00000000586: Intron |
C | T |
homozygote
|
MACSNP016072229848 | chr20: 6160 | SM2 |
ENSMMUG00000000586: Intron |
G | T |
heterozygote
|
MACSNP016072229852 | chr20: 7174 | SM2 |
ENSMMUG00000000586: Intron |
A | C |
heterozygote
|
MACSNP016072229859 | chr20: 7582 | SM2 |
ENSMMUG00000000586: Intron |
C | G |
heterozygote
|
MACSNP016072229861 | chr20: 7737 | SM2 |
ENSMMUG00000000586: Intron |
G | T |
heterozygote
|