NM_005006.7(NDUFS1):c.414T>C (p.Asp138=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Sep 13, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000127138.6
Allele description [Variation Report for NM_005006.7(NDUFS1):c.414T>C (p.Asp138=)]
NM_005006.7(NDUFS1):c.414T>C (p.Asp138=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024