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中文
这个突变被确定为在exon 10的第1092位，由C变为A的替换。产生的蛋白质在第310位氨基酸位置有一个酪氨酸到终止密码子的替换。这个突变位于P/S/T功能区域(来源：J:73625)。
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
