NM_000433.4(NCF2):c.1462T>C (p.Ser488Pro) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002592582.2
Allele description [Variation Report for NM_000433.4(NCF2):c.1462T>C (p.Ser488Pro)]
NM_000433.4(NCF2):c.1462T>C (p.Ser488Pro)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Hordeum vulgare f. agriocrithon
Hordeum vulgare f. agriocrithonbiosample
-
Homologene neighbors for GEO Profiles (Select 63838244) (0)
GEO Profiles
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024