NM_001166347.2(SLC26A11):c.545C>T (p.Pro182Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004237999.1
Allele description [Variation Report for NM_001166347.2(SLC26A11):c.545C>T (p.Pro182Leu)]
NM_001166347.2(SLC26A11):c.545C>T (p.Pro182Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024