Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP019036100632 | chr8: 223132 | LM1 | Intergenic | T | A |
heterozygote
|
MACSNP019036100659 | chr8: 395394 | LM1 |
ENSMMUG00000011105: Intron |
G | C |
heterozygote
|
MACSNP019036100662 | chr8: 395413 | LM1 |
ENSMMUG00000011105: Intron |
G | A |
homozygote
|
MACSNP019036100665 | chr8: 395455 | LM1 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP019036100670 | chr8: 395511 | LM1 |
ENSMMUG00000011105: Intron |
T | C |
homozygote
|
MACSNP019036100685 | chr8: 395904 | LM1 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP019036100693 | chr8: 396111 | LM1 |
ENSMMUG00000011105: Intron |
T | C |
heterozygote
|
MACSNP019036100698 | chr8: 396171 | LM1 |
ENSMMUG00000011105: Intron |
A | G |
homozygote
|
MACSNP019036100703 | chr8: 396371 | LM1 |
ENSMMUG00000011105: Intron |
T | C |
homozygote
|
MACSNP019036100705 | chr8: 396471 | LM1 |
ENSMMUG00000011105: Intron |
C | T |
homozygote
|