NM_016175.4(MRNIP):c.692A>G (p.Gln231Arg) AND Paget disease of bone 3
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000391145.5
Allele description [Variation Report for NM_016175.4(MRNIP):c.692A>G (p.Gln231Arg)]
NM_016175.4(MRNIP):c.692A>G (p.Gln231Arg)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023