NM_001127258.3(HHIPL1):c.1885C>T (p.Arg629Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 8, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004119326.1
Allele description [Variation Report for NM_001127258.3(HHIPL1):c.1885C>T (p.Arg629Cys)]
NM_001127258.3(HHIPL1):c.1885C>T (p.Arg629Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024