NM_020937.4(FANCM):c.4627C>T (p.Leu1543Phe) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 24, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001820930.11
Allele description [Variation Report for NM_020937.4(FANCM):c.4627C>T (p.Leu1543Phe)]
NM_020937.4(FANCM):c.4627C>T (p.Leu1543Phe)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024