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中文
这种在9:15067150(GRCh38.p6)位置的自发插入一个A，预测会导致第14外显子的框移，改变820-826位的氨基酸编码，接着是过早终止，以及通过 nonsense-mediated decay(ND)处理。(来源：J:276072)
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
