NM_000490.5(AVP):c.363C>T (p.His121=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000923001.7
Allele description [Variation Report for NM_000490.5(AVP):c.363C>T (p.His121=)]
NM_000490.5(AVP):c.363C>T (p.His121=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024