NM_017780.4(CHD7):c.7952A>G (p.Asn2651Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 21, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001785541.2
Allele description [Variation Report for NM_017780.4(CHD7):c.7952A>G (p.Asn2651Ser)]
NM_017780.4(CHD7):c.7952A>G (p.Asn2651Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 2, 2024