NM_001139.3(ALOX12B):c.1566G>T (p.Pro522=) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Apr 27, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000791166.8
Allele description [Variation Report for NM_001139.3(ALOX12B):c.1566G>T (p.Pro522=)]
NM_001139.3(ALOX12B):c.1566G>T (p.Pro522=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Feb 4, 2024