NM_020975.6(RET):c.951G>A (p.Thr317=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000251081.6
Allele description [Variation Report for NM_020975.6(RET):c.951G>A (p.Thr317=)]
NM_020975.6(RET):c.951G>A (p.Thr317=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024