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Varaico: Literature-Extracted Genetic Variants
hg38
Include likely false extractions
Gene:
TRIM27
Variant:
p.E307Splc
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TRIM27
NM_006510.5:p.E307Splc
hg38:chr6:28907264 T>C
Frequencies & domains
Associated Papers
New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.
Cox TC et al.
Human Molecular Genetics,
2000
11030761 (PubMed
)
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