NM_001267550.2(TTN):c.48727C>T (p.Pro16243Ser) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001081356.16
Allele description [Variation Report for NM_001267550.2(TTN):c.48727C>T (p.Pro16243Ser)]
NM_001267550.2(TTN):c.48727C>T (p.Pro16243Ser)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024