NM_014930.3(ZNF510):c.682C>T (p.His228Tyr) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004187624.1
Allele description [Variation Report for NM_014930.3(ZNF510):c.682C>T (p.His228Tyr)]
NM_014930.3(ZNF510):c.682C>T (p.His228Tyr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024