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PRR23C

Synonyms
-
External resources

Variant Counts

Variant classification counts, according to ACMG guideline on all identified variants among our tested samples, are listed. The variants with over 5% variant frequency in population genome databases ( gnomAD, dbSNP, etc.) are excluded.

Pathogenic
32
Likely pathogenic
0
VUS
694
Likely benign
14
Benign
0

Patient Phenotypes

Proportions of phenotypes among 32 patients carrying pathogenic or likely pathogenic variants on PRR23C gene are displayed below. The following symptoms were found in patients with a variant in PRR23C. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
43.8%
Abnormality of the musculoskeletal system
25%
Abnormality of the cardiovascular system
21.9%
Abnormality of the immune system
15.6%
Abnormality of head or neck
12.5%
Abnormality of the integument
12.5%
Growth abnormality
12.5%
Abnormality of blood and blood forming tissues
9.4%
Abnormality of metabolism homeostasis
9.4%
Abnormality of the ear
9.4%
Abnormality of the eye
9.4%
Abnormality of the digestive system
6.3%
Abnormality of the genitourinary system
6.3%
Neoplasm
6.3%
Abnormality of limbs
3.1%
Abnormality of prenatal development or birth
3.1%
Abnormality of the respiratory system
3.1%
Abnormality of the voice
3.1%
Constitutional symptom
3.1%
Abnormal cellular phenotype
0%
Abnormality of the breast
0%
Abnormality of the endocrine system
0%
Abnormality of the thoracic cavity
0%

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