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EN
SNP rs8281486 is a G-to-A mutation at ChrM:9348 that changes valine codon 248 to an isoleucine codon (p.V248I). This mutation is found in the A/J, BALB/cJ, BALB/cByJ, BPL/1J, CBA/J, C3H/HeJ, C3H/He, I/LnJ, LT/SvEi, NOD/LtJ, SEA/GnJ, SEA/GnJ, and STR/ort strains. (J:143901)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
