NM_017635.5(KMT5B):c.2020G>A (p.Gly674Ser) AND Intellectual disability, autosomal dominant 51
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 23, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003138860.3
Allele description [Variation Report for NM_017635.5(KMT5B):c.2020G>A (p.Gly674Ser)]
NM_017635.5(KMT5B):c.2020G>A (p.Gly674Ser)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024