Home > Gene Browser > TBC1D3L

TBC1D3L

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
30
Likely pathogenic
0
VUS
3,650
Likely benign
1,989
Benign
0

Patient Phenotypes

Proportions of phenotypes among 29 patients carrying pathogenic or likely pathogenic variants on TBC1D3L gene are displayed below. The following symptoms were found in patients with a variant in TBC1D3L. However, patients may have been diagnosed with a different variant.

Phenotype class
Patients in 3billion (%)
Abnormality of the nervous system
37.9%
Abnormality of head or neck
27.6%
Abnormality of the ear
27.6%
Abnormality of the eye
27.6%
Abnormality of the cardiovascular system
24.1%
Abnormality of the integument
24.1%
Abnormality of the musculoskeletal system
24.1%
Abnormality of limbs
13.8%
Abnormality of the endocrine system
13.8%
Abnormality of metabolism homeostasis
6.9%
Abnormality of the genitourinary system
6.9%
Growth abnormality
6.9%
Abnormality of blood and blood forming tissues
3.4%
Abnormality of the breast
3.4%
Abnormality of the respiratory system
3.4%
Abnormal cellular phenotype
0%
Abnormality of prenatal development or birth
0%
Abnormality of the digestive system
0%
Abnormality of the immune system
0%
Abnormality of the thoracic cavity
0%
Abnormality of the voice
0%
Constitutional symptom
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.