Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP018036100654 | chr8: 234711 | PM2 |
ENSMMUG00000020598: Intron |
A | G |
heterozygote
|
MACSNP018036100666 | chr8: 395461 | PM2 |
ENSMMUG00000011105: Intron |
T | C |
heterozygote
|
MACSNP018036100667 | chr8: 395472 | PM2 |
ENSMMUG00000011105: Intron |
T | C |
heterozygote
|
MACSNP018036100670 | chr8: 395511 | PM2 |
ENSMMUG00000011105: Intron |
T | C |
homozygote
|
MACSNP018036100681 | chr8: 395714 | PM2 |
ENSMMUG00000011105: Intron |
C | T |
heterozygote
|
MACSNP018036100682 | chr8: 395770 | PM2 |
ENSMMUG00000011105: Intron |
T | C |
heterozygote
|
MACSNP018036100684 | chr8: 395865 | PM2 |
ENSMMUG00000011105: Intron |
T | A |
heterozygote
|
MACSNP018036100685 | chr8: 395904 | PM2 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP018036100690 | chr8: 396074 | PM2 |
ENSMMUG00000011105: Intron |
G | T |
heterozygote
|
MACSNP018036100698 | chr8: 396171 | PM2 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|