NM_000035.4(ALDOB):c.759C>T (p.Thr253=) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Nov 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000372800.6
Allele description [Variation Report for NM_000035.4(ALDOB):c.759C>T (p.Thr253=)]
NM_000035.4(ALDOB):c.759C>T (p.Thr253=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 20, 2024