NM_003482.4(KMT2D):c.15230T>C (p.Leu5077Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 10, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000178654.4
Allele description [Variation Report for NM_003482.4(KMT2D):c.15230T>C (p.Leu5077Pro)]
NM_003482.4(KMT2D):c.15230T>C (p.Leu5077Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024