NM_000512.5(GALNS):c.106C>T (p.Leu36=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001531863.20
Allele description [Variation Report for NM_000512.5(GALNS):c.106C>T (p.Leu36=)]
NM_000512.5(GALNS):c.106C>T (p.Leu36=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024