NM_003000.3(SDHB):c.597C>T (p.Tyr199=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 14, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000934713.1
Allele description
NM_003000.3(SDHB):c.597C>T (p.Tyr199=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Jul 2, 2022