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中文
这个分子异常发生在染色体11的第59,565,850位(A-G)转换，或者在GenBank的NC_000077基因组区域的第24,282位，对应于NM_145827 mRNA序列中的第3,063个核苷酸，位于10个总exons中的第4个外显子。这个变异导致NLRP3蛋白中第946位的天冬氨酸(D)被甘氨酸(G)替换，Polyphen-2预测为良性(评分为0.017)。(来源：J:216047)
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
