NM_001130045.2(TTLL10):c.53C>T (p.Thr18Ile) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004149183.1
Allele description [Variation Report for NM_001130045.2(TTLL10):c.53C>T (p.Thr18Ile)]
NM_001130045.2(TTLL10):c.53C>T (p.Thr18Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024