NM_130849.4(SLC39A4):c.999C>T (p.Ala333=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 11, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003045381.3
Allele description [Variation Report for NM_130849.4(SLC39A4):c.999C>T (p.Ala333=)]
NM_130849.4(SLC39A4):c.999C>T (p.Ala333=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024