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中文
AC>C帧移是因为在染色体16的v38版本中1个碱基对(19,956,966)的缺失，或者在GenBank的NC_000082基因组区域的第26,083位。这个变异对应于mRNA序列NM_183390中c.888delA的位置，位于7个总exons的第3个exon内。预测的蛋白质产物会因为这个帧移开始于第279位，并在包含40个异常氨基酸后终止。(来源：J:274963)
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
