NM_001101677.2(SOHLH1):c.1082C>T (p.Pro361Leu) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 24, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000961981.4
Allele description [Variation Report for NM_001101677.2(SOHLH1):c.1082C>T (p.Pro361Leu)]
NM_001101677.2(SOHLH1):c.1082C>T (p.Pro361Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024