NM_002180.3(IGHMBP2):c.2025C>T (p.Thr675=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 9, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000430376.11
Allele description [Variation Report for NM_002180.3(IGHMBP2):c.2025C>T (p.Thr675=)]
NM_002180.3(IGHMBP2):c.2025C>T (p.Thr675=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 20, 2024