NM_176812.5(CHMP4B):c.439A>G (p.Thr147Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004111345.1
Allele description [Variation Report for NM_176812.5(CHMP4B):c.439A>G (p.Thr147Ala)]
NM_176812.5(CHMP4B):c.439A>G (p.Thr147Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024