NM_017780.4(CHD7):c.6111C>T (p.Pro2037=) AND not provided
- Germline classification:
- Benign (4 submissions)
- Last evaluated:
- Mar 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000857516.23
Allele description [Variation Report for NM_017780.4(CHD7):c.6111C>T (p.Pro2037=)]
NM_017780.4(CHD7):c.6111C>T (p.Pro2037=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 20, 2024