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中文
这个突变发生在染色体5的第140,906,767个核苷酸（v38），或者在GenBank的基因组区域NC_000071中的第93,830位。在mRNA序列NM_175362的第5个外显子中，这个突变对应于第863位的氨基酸（Y181C）。引用信息为(J:221487)。
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
