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IGDCC3

Synonyms
HsT18880, PUNC
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
35
Likely pathogenic
0
VUS
3,814
Likely benign
459
Benign
0

Patient phenotypes

Proportions of phenotypes among 35 patients carring pathogenic or likely pathogenic variants on IGDCC3 gene are displayed below.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
40%
Abnormality of the cardiovascular system
25.7%
Abnormality of the musculoskeletal system
22.9%
Abnormality of the eye
20%
Abnormality of head or neck
14.3%
Growth abnormality
14.3%
Abnormality of limbs
11.4%
Abnormality of the ear
11.4%
Abnormality of the immune system
8.6%
Abnormality of blood and blood-forming tissues
5.7%
Abnormality of the digestive system
5.7%
Abnormality of prenatal development or birth
2.9%
Abnormality of the endocrine system
2.9%
Abnormality of the genitourinary system
2.9%
Neoplasm
2.9%
Abnormal cellular phenotype
0%
Abnormality of metabolism homeostasis
0%
Abnormality of the breast
0%
Abnormality of the integument
0%
Abnormality of the respiratory system
0%
Abnormality of the thoracic cavity
0%
Abnormality of the voice
0%
Constitutional symptom
0%

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