NM_170606.3(KMT2C):c.53C>T (p.Pro18Leu) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 31, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002015640.4
Allele description [Variation Report for NM_170606.3(KMT2C):c.53C>T (p.Pro18Leu)]
NM_170606.3(KMT2C):c.53C>T (p.Pro18Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024