NM_000390.4(CHM):c.825G>A (p.Pro275=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 16, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000870871.9
Allele description [Variation Report for NM_000390.4(CHM):c.825G>A (p.Pro275=)]
NM_000390.4(CHM):c.825G>A (p.Pro275=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024