NM_022041.4(GAN):c.1416G>A (p.Val472=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001311453.21
Allele description [Variation Report for NM_022041.4(GAN):c.1416G>A (p.Val472=)]
NM_022041.4(GAN):c.1416G>A (p.Val472=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024