NM_001025389.2(AMPD3):c.1824C>T (p.His608=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 5, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000174267.4
Allele description [Variation Report for NM_001025389.2(AMPD3):c.1824C>T (p.His608=)]
NM_001025389.2(AMPD3):c.1824C>T (p.His608=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023