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SOBP

Synonyms
JXC1, MRAMS
External resources
Summary
The protein encoded by this gene is a nuclear zinc finger protein that is involved in development of the cochlea. Defects in this gene have also been linked to intellectual disability.

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
0
Likely pathogenic
0
VUS
1,917
Likely benign
317
Benign
282

Patient phenotypes

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

Phenotype class
Patients in 3billion (%)

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