NM_130770.3(HTR3C):c.1097del (p.Gln366fs) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 2, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000885175.3
Allele description [Variation Report for NM_130770.3(HTR3C):c.1097del (p.Gln366fs)]
NM_130770.3(HTR3C):c.1097del (p.Gln366fs)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023