Home > Gene Browser > ARHGAP33

ARHGAP33

Synonyms
NOMA-GAP, SNX26, TCGAP
External resources
Summary
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Alternative splice variants encoding different isoforms have been identified in this gene.

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
0
Likely pathogenic
0
VUS
3,321
Likely benign
11,975
Benign
0

Patient phenotypes

No patients carry pathogenic or likely pathogenic variants on ARHGAP33 gene.

Phenotype class
Patients in 3billion (%)

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