NM_001267550.2(TTN):c.98685T>C (p.Asn32895=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 15, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001487197.5
Allele description [Variation Report for NM_001267550.2(TTN):c.98685T>C (p.Asn32895=)]
NM_001267550.2(TTN):c.98685T>C (p.Asn32895=)
Condition(s)
Assertion and evidence details
Last Updated: Aug 5, 2023