NM_002180.3(IGHMBP2):c.2322A>G (p.Glu774=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Dec 21, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000420667.1
Allele description [Variation Report for NM_002180.3(IGHMBP2):c.2322A>G (p.Glu774=)]
NM_002180.3(IGHMBP2):c.2322A>G (p.Glu774=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 5, 2024