NM_031935.3(HMCN1):c.114G>T (p.Gly38=) AND not provided
- Germline classification:
- Benign/Likely benign (5 submissions)
- Last evaluated:
- Jan 18, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000954222.19
Allele description [Variation Report for NM_031935.3(HMCN1):c.114G>T (p.Gly38=)]
NM_031935.3(HMCN1):c.114G>T (p.Gly38=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024