NM_015382.4(HECTD1):c.2782A>G (p.Met928Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004234564.1
Allele description [Variation Report for NM_015382.4(HECTD1):c.2782A>G (p.Met928Val)]
NM_015382.4(HECTD1):c.2782A>G (p.Met928Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 18, 2024