NM_014877.4(HELZ):c.4448T>C (p.Ile1483Thr) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004117474.1
Allele description [Variation Report for NM_014877.4(HELZ):c.4448T>C (p.Ile1483Thr)]
NM_014877.4(HELZ):c.4448T>C (p.Ile1483Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024