NM_001267550.2(TTN):c.106117C>T (p.Gln35373Ter) AND multiple conditions
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Dec 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001975648.4
Allele description [Variation Report for NM_001267550.2(TTN):c.106117C>T (p.Gln35373Ter)]
NM_001267550.2(TTN):c.106117C>T (p.Gln35373Ter)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024