NM_001164508.2(NEB):c.21751C>G (p.Gln7251Glu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 8, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000238962.5
Allele description [Variation Report for NM_001164508.2(NEB):c.21751C>G (p.Gln7251Glu)]
NM_001164508.2(NEB):c.21751C>G (p.Gln7251Glu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 16, 2025