NM_173808.3(NEGR1):c.740G>C (p.Gly247Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004152786.1
Allele description [Variation Report for NM_173808.3(NEGR1):c.740G>C (p.Gly247Ala)]
NM_173808.3(NEGR1):c.740G>C (p.Gly247Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024