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FAT3

Synonyms
CDHF15, CDHR10, hFat3
External resources
Summary
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Variant counts

The variants found in rare patients tested by 3billion are classified and counted according to ACMG guidelines. The variants with over 5% variant frequency in population genome databases ( gnomAD, dbSNP, etc) are excluded.

Pathogenic
11
Likely pathogenic
0
VUS
18,032
Likely benign
4,616
Benign
0

Patient phenotypes

Proportions of phenotypes among 9 patients carrying pathogenic or likely pathogenic variants on FAT3 gene are displayed below.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
33.3%
Abnormality of the cardiovascular system
22.2%
Abnormality of the ear
22.2%
Abnormality of the eye
22.2%
Abnormality of the immune system
22.2%
Abnormality of the musculoskeletal system
22.2%
Abnormal cellular phenotype
11.1%
Abnormality of blood and blood-forming tissues
11.1%
Abnormality of head or neck
11.1%
Abnormality of limbs
11.1%
Abnormality of the digestive system
11.1%
Abnormality of the integument
11.1%
Growth abnormality
11.1%
Abnormality of metabolism homeostasis
0%
Abnormality of prenatal development or birth
0%
Abnormality of the breast
0%
Abnormality of the endocrine system
0%
Abnormality of the genitourinary system
0%
Abnormality of the respiratory system
0%
Abnormality of the thoracic cavity
0%
Abnormality of the voice
0%
Constitutional symptom
0%
Neoplasm
0%

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