NM_004629.2(FANCG):c.640C>T (p.Arg214Cys) AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Mar 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000121040.10
Allele description [Variation Report for NM_004629.2(FANCG):c.640C>T (p.Arg214Cys)]
NM_004629.2(FANCG):c.640C>T (p.Arg214Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024