NM_206937.2(LIG4):c.2016C>G (p.Ser672Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 29, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000193141.6
Allele description [Variation Report for NM_206937.2(LIG4):c.2016C>G (p.Ser672Arg)]
NM_206937.2(LIG4):c.2016C>G (p.Ser672Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024