NM_005199.5(CHRNG):c.951C>A (p.Ile317=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Dec 10, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000180614.9
Allele description [Variation Report for NM_005199.5(CHRNG):c.951C>A (p.Ile317=)]
NM_005199.5(CHRNG):c.951C>A (p.Ile317=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024