NM_021830.5(TWNK):c.1366C>G (p.Leu456Val) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jun 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000415948.21
Allele description [Variation Report for NM_021830.5(TWNK):c.1366C>G (p.Leu456Val)]
NM_021830.5(TWNK):c.1366C>G (p.Leu456Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024