NM_002764.4(PRPS1):c.447G>A (p.Pro149=) AND not specified
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Feb 19, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000440183.9
Allele description [Variation Report for NM_002764.4(PRPS1):c.447G>A (p.Pro149=)]
NM_002764.4(PRPS1):c.447G>A (p.Pro149=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024