NM_025193.4(HSD3B7):c.357C>T (p.Thr119=) AND not provided
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Nov 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000957961.14
Allele description [Variation Report for NM_025193.4(HSD3B7):c.357C>T (p.Thr119=)]
NM_025193.4(HSD3B7):c.357C>T (p.Thr119=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 17, 2024