NM_001267550.2(TTN):c.83571C>T (p.Pro27857=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000470533.9
Allele description [Variation Report for NM_001267550.2(TTN):c.83571C>T (p.Pro27857=)]
NM_001267550.2(TTN):c.83571C>T (p.Pro27857=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024