NM_001277115.2(DNAH11):c.8266T>C (p.Cys2756Arg) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 2, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000251345.9
Allele description [Variation Report for NM_001277115.2(DNAH11):c.8266T>C (p.Cys2756Arg)]
NM_001277115.2(DNAH11):c.8266T>C (p.Cys2756Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 15, 2024