NM_145260.3(OSR1):c.181G>A (p.Ala61Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004125511.1
Allele description [Variation Report for NM_145260.3(OSR1):c.181G>A (p.Ala61Thr)]
NM_145260.3(OSR1):c.181G>A (p.Ala61Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024