NM_005262.3(GFER):c.393G>A (p.Gln131=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002637915.3
Allele description [Variation Report for NM_005262.3(GFER):c.393G>A (p.Gln131=)]
NM_005262.3(GFER):c.393G>A (p.Gln131=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024