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中文
一个单个碱基对的突变导致编码蛋白质的第335位由苯丙氨酸变为亮氨酸，这种非保守的序列变化。突变蛋白在与其他突变等位基因的遗传交互测试中表现出过量表型活性。(来源：J:92947)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
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
