NM_020975.6(RET):c.1119G>A (p.Ala373=) AND not provided
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Mar 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000679710.21
Allele description [Variation Report for NM_020975.6(RET):c.1119G>A (p.Ala373=)]
NM_020975.6(RET):c.1119G>A (p.Ala373=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024