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中文
在chrM:11780位置的一个T到A的突变，将异亮氨酸密码子(ATT)替换为甲硫氨酸密码子( mitochondrial ATA)，导致第13位氨基酸变为甲硫氨酸( p.I13M)。这个突变存在于VM菌株中。(来源：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
