NM_021083.4(XK):c.657T>C (p.Ile219=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003015130.2
Allele description [Variation Report for NM_021083.4(XK):c.657T>C (p.Ile219=)]
NM_021083.4(XK):c.657T>C (p.Ile219=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024