NM_000514.4(GDNF):c.429G>A (p.Arg143=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Feb 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001657856.7
Allele description [Variation Report for NM_000514.4(GDNF):c.429G>A (p.Arg143=)]
NM_000514.4(GDNF):c.429G>A (p.Arg143=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 10, 2024