Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP016036100663 | chr8: 395439 | SM2 |
ENSMMUG00000011105: Intron |
G | A |
homozygote
|
MACSNP016036100673 | chr8: 395585 | SM2 |
ENSMMUG00000011105: Intron |
G | A |
homozygote
|
MACSNP016036100685 | chr8: 395904 | SM2 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP016036100698 | chr8: 396171 | SM2 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP016036100701 | chr8: 396338 | SM2 |
ENSMMUG00000011105: Intron |
G | A |
homozygote
|
MACSNP016036100703 | chr8: 396371 | SM2 |
ENSMMUG00000011105: Intron |
T | C |
homozygote
|
MACSNP016036100710 | chr8: 396590 | SM2 |
ENSMMUG00000011105: Intron |
T | G |
homozygote
|
MACSNP016036100723 | chr8: 397000 | SM2 |
ENSMMUG00000011105: Intron |
G | A |
homozygote
|
MACSNP016036100724 | chr8: 397048 | SM2 |
ENSMMUG00000011105: Intron |
T | C |
homozygote
|
MACSNP016036100732 | chr8: 397231 | SM2 |
ENSMMUG00000011105: Intron |
G | T |
homozygote
|