NM_001267550.2(TTN):c.99197C>G (p.Ala33066Gly) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 15, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001059537.7
Allele description [Variation Report for NM_001267550.2(TTN):c.99197C>G (p.Ala33066Gly)]
NM_001267550.2(TTN):c.99197C>G (p.Ala33066Gly)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024