Individual SNV ID | Position | Inidvidual | Gene: Location | Reference | Alteration | Genotype |
---|---|---|---|---|---|---|
MACSNP017072229825 | chr20: 5199 | PM1 |
ENSMMUG00000000586: Intron |
T | C |
homozygote
|
MACSNP017072229831 | chr20: 5457 | PM1 |
ENSMMUG00000000586: Intron |
T | C |
homozygote
|
MACSNP017072229840 | chr20: 5806 | PM1 |
ENSMMUG00000000586: Intron |
C | T |
homozygote
|
MACSNP017072229842 | chr20: 5897 | PM1 |
ENSMMUG00000000586: Intron |
C | G |
homozygote
|
MACSNP017072229847 | chr20: 6157 | PM1 |
ENSMMUG00000000586: Intron |
A | G |
heterozygote
|
MACSNP017072229857 | chr20: 7496 | PM1 |
ENSMMUG00000000586: Intron |
C | T |
heterozygote
|
MACSNP017072229864 | chr20: 8358 | PM1 |
ENSMMUG00000000586: Intron |
C | T |
homozygote
|
MACSNP017072229876 | chr20: 8736 | PM1 |
ENSMMUG00000000586: Intron |
A | C |
heterozygote
|
MACSNP017072229878 | chr20: 8790 | PM1 |
ENSMMUG00000000586: Intron |
T | C |
heterozygote
|
MACSNP017072229879 | chr20: 8816 | PM1 |
ENSMMUG00000000586: Intron |
C | A |
heterozygote
|