NM_003922.4(HERC1):c.13677C>T (p.Tyr4559=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002996688.2
Allele description [Variation Report for NM_003922.4(HERC1):c.13677C>T (p.Tyr4559=)]
NM_003922.4(HERC1):c.13677C>T (p.Tyr4559=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024