Home > Gene Browser > COMMD4

COMMD4

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
103
Likely pathogenic
0
VUS
4,616
Likely benign
0
Benign
0

Patient Phenotypes

Proportions of phenotypes among 32 patients carrying pathogenic or likely pathogenic variants on COMMD4 gene are displayed below. The following symptoms were found in patients with a variant in COMMD4. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of blood and blood forming tissues
25%
Abnormality of the nervous system
25%
Abnormality of the eye
21.9%
Abnormality of head or neck
18.8%
Abnormality of the musculoskeletal system
15.6%
Abnormality of the cardiovascular system
9.4%
Abnormality of the ear
9.4%
Abnormality of the immune system
9.4%
Abnormality of the integument
9.4%
Abnormality of limbs
6.3%
Abnormality of the digestive system
6.3%
Abnormality of the respiratory system
6.3%
Abnormality of metabolism homeostasis
3.1%
Abnormality of prenatal development or birth
3.1%
Abnormality of the genitourinary system
3.1%
Constitutional symptom
3.1%
Growth abnormality
3.1%
Abnormal cellular phenotype
0%
Abnormality of the breast
0%
Abnormality of the endocrine system
0%
Abnormality of the thoracic cavity
0%
Abnormality of the voice
0%
Neoplasm
0%

Have a question or need assistance? Ask here.

Send us your questions or comments related to the variant counts and/or patient phenotypes.