NM_001025930.5(TTLL3):c.238G>A (p.Gly80Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004079651.1
Allele description [Variation Report for NM_001025930.5(TTLL3):c.238G>A (p.Gly80Ser)]
NM_001025930.5(TTLL3):c.238G>A (p.Gly80Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024