NM_004629.2(FANCG):c.739C>A (p.Gln247Lys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 16, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000500656.6
Allele description [Variation Report for NM_004629.2(FANCG):c.739C>A (p.Gln247Lys)]
NM_004629.2(FANCG):c.739C>A (p.Gln247Lys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024