NM_014727.3(KMT2B):c.2268_2279dup (p.Gln759_Pro762dup) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (5 submissions)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000996841.24
Allele description [Variation Report for NM_014727.3(KMT2B):c.2268_2279dup (p.Gln759_Pro762dup)]
NM_014727.3(KMT2B):c.2268_2279dup (p.Gln759_Pro762dup)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024