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中文
这个描述的变异发生在人类基因1的v38位置，具体是133,012,651号碱基对，或者在NC_000067的GenBank基因组区域的17,937号位置。这个变异会导致Mdm4基因的第416位氨基酸由phe变为ile，即F47I。这个信息来源于文献(J:265262)。
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
