NM_000112.4(SLC26A2):c.1761C>T (p.Leu587=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000250262.5
Allele description [Variation Report for NM_000112.4(SLC26A2):c.1761C>T (p.Leu587=)]
NM_000112.4(SLC26A2):c.1761C>T (p.Leu587=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024