NM_014727.3(KMT2B):c.7052C>T (p.Pro2351Leu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002653525.2
Allele description [Variation Report for NM_014727.3(KMT2B):c.7052C>T (p.Pro2351Leu)]
NM_014727.3(KMT2B):c.7052C>T (p.Pro2351Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024