NM_004168.4(SDHA):c.17G>A (p.Gly6Asp) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- May 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000216190.11
Allele description [Variation Report for NM_004168.4(SDHA):c.17G>A (p.Gly6Asp)]
NM_004168.4(SDHA):c.17G>A (p.Gly6Asp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024